314 Scientific Writing Jobs

As a Medical Writer at Novartis, your role involves writing, supporting, and managing projects to prepare high-quality medical and scientific communications. This includes conducting literature reviews, creating abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or internal medical and clinical team meetings. Your key responsibilities will include: - Preparing literature reviews, abstracts, posters, slide sets, and complex manuscripts using data from various sources such as clinical study reports and patient profiles. - Performing quality control checks and proofreading deliverables to ensure they meet customer expectations. - Managing multiple projects simultaneously, focusing on up to two brands at a time. - Obtaining feedback from customers and implementing customer management tactics. - Following Novartis specifications for documentation and tracking clinical trial milestones for assigned projects. - Maintaining records for all projects, including archiving and ensuring audit, SOP, and training compliance. - Training new team members and colleagues when required, in addition to performing any other assigned tasks. The minimum requirements for this role are: - Science degree or equivalent, B.Sc./equivalent with 8 years of Clinical Research (CR) experience, or M.Sc./M.Pharm +6 years of clinical research (CR) experience. - Desired qualifications include a Doctoral Degree or a Qualification in Medical Sciences (MBBS/MD/equivalent). - Alternatively, a PhD + 4 years of CR experience, MBBS/equivalent + 4 years of CR experience, or MD + 2 years of CR experience. Novartis is dedicated to reimagining medicine to improve and extend people's lives. By becoming a part of Novartis, you will contribute to our vision of becoming the most valued and trusted medicines company globally. If you are ready to join a mission-driven organization with a commitment to diversity and inclusion, consider applying to be a Medical Writer at Novartis. To learn more about our company culture and career opportunities, visit: [Novartis People and Culture](https://www.novartis.com/about/strategy/people-and-culture). Explore our benefits and rewards in the Novartis Life Handbook: [Novartis Benefits and Rewards](https://www.novartis.com/careers/benefits-rewards). Join the Novartis Network to stay connected and receive updates on future career opportunities: [Novartis Network](https://talentnetwork.novartis.com/network). As a Medical Writer at Novartis, your role involves writing, supporting, and managing projects to prepare high-quality medical and scientific communications. This includes conducting literature reviews, creating abstracts, posters, slide sets, and complex manuscripts for publication or presentation at congresses or internal medical and clinical team meetings. Your key responsibilities will include: - Preparing literature reviews, abstracts, posters, slide sets, and complex manuscripts using data from various sources such as clinical study reports and patient profiles. - Performing quality control checks and proofreading deliverables to ensure they meet customer expectations. - Managing multiple projects simultaneously, focusing on up to two brands at a time. - Obtaining feedback from customers and implementing customer management tactics. - Following Novartis specifications for documentation and tracking clinical trial milestones for assigned projects. - Maintaining records for all projects, including archiving and ensuring audit, SOP, and training compliance. - Training new team members and colleagues when required, in addition to performing any other assigned tasks. The minimum requirements for this role are: - Science degree or equivalent, B.Sc./equivalent with 8 years of Clinical Research (CR) experience, or M.Sc./M.Pharm +6 years of clinical research (CR) experience. - Desired qualifications include a Doctoral Degree or a Qualification in Medical Sciences (MBBS/MD/equivalent). - Alternatively, a PhD + 4 years of CR experience, MBBS/equivalent + 4 years of CR experience, or MD + 2 years of CR experience. Novartis is dedicated to reimagining medicine to improve and extend people's lives. By becoming a part of Novartis, you will contribute to our vision of becoming the most valued and trusted medicines company globally. If you are ready to join a mission-driven organization with a commitment to diversity and inclusion, consider applying to be a Medical Writer at Novartis. To learn more about our company culture and career opportunities, visit: [Novartis People and Culture](https://www.novartis.com/about/strategy/people-and-culture). Explore our benefits and rewards in the Novartis Life Handbook: [Novartis Benefits and Rewards](https://www.novartis.com/careers/benefits-rewards). Join the Novartis Network to stay connected and receive updates on future career opportunities: [Novartis Network](https://talentnetwork.novartis.com/network).

Role Overview: As a Remote Consultant Senior Medical Writer at our company, you will be responsible for writing regulatory clinical documents such as clinical trial reports, investigators brochures, summary documents, and other documents covering interpretation and documentation of clinical data. You should have a Masters Degree in Pharmacy or Medicine with a minimum of 7 to 9 years of experience in Medical Writing. Your expertise in scientific research methods and scientific writing skills will be crucial in this role. Additionally, you must have excellent written and spoken English skills at a professional level, along with a genuine interest in scientific communication. Key Responsibilities: - Write regulatory clinical documents including clinical trial reports, investigators brochures, and summary documents - Interpret and document clinical data effectively - Demonstrate expertise in scientific research methods and scientific writing skills - Ensure all documents meet regulatory requirements and guidelines - Collaborate with cross-functional teams to ensure accuracy and completeness of documents Qualifications Required: - Masters Degree in Pharmacy or Medicine - Minimum 7 to 9 years of experience in Medical Writing - Strong written and spoken English skills at a professional level - Demonstrated expertise in scientific research methods and scientific writing - Genuine interest in scientific communication Please email your resume in pdf or doc format to career@ancillarie.com if you are ready to take on challenges, turn opportunities into success, and aim to excel in your career.,

Role Overview: You will be joining the Global Scientific Communications Content Hub team as a Scientific Writer. This team is responsible for developing medical communications, medical education, and medical information content in collaboration with various teams across Healthcare R&D, focusing on key therapy areas such as Oncology, Neurology & Immunology, Fertility, Cardio-metabolic, and Endocrinology. Key Responsibilities: - Independently develop high-quality medical information documents (e.g., Global Response Documents, Medical Inquiries, FAQs, etc.) following defined processes and timelines. - Contribute actively to improvement initiatives within the Global Scientific Communications Content Hub and Medical Information teams. - Demonstrate a successful track record in scientific writing, capable of developing various content types simultaneously and prioritizing tasks to meet deadlines. - Stay informed about emerging trends in the scientific communications field. - Possess strong analytical skills to comprehend complex scientific datasets effectively. Qualifications Required: - 1-3 years of professional experience in preparing medical information materials within an international Pharma/Biotech/agency setting. - Hold an advanced university degree in science, medicine, or a related field. - Therapeutic expertise/experience in at least one of the organization's key therapy areas, with a preference for Oncology and knowledge in Neurology and Immunology, Fertility, Cardio-metabolic, and Endocrinology. Additional Details: You will have the opportunity to work in a diverse, inclusive, and flexible culture that encourages personal development and career advancement globally. The company values a variety of backgrounds, perspectives, and life experiences, believing that this diversity fosters excellence and innovation in leading science and technology. By joining this team, you will contribute to creating a culture of inclusion and belonging, impacting millions and empowering individuals to drive human progress through sparking discovery and elevating humanity. Apply now to be part of a team dedicated to these aspirations!,

You will be joining Axtria, a global provider of cloud software and data analytics to the life sciences industry, with a commitment to transforming product commercialization for improved healthcare outcomes. The company is dedicated to aligning operations with universal principles and advancing societal goals. As a member of the team, you will contribute to projects related to literature reviews, scientific publications, and market access documents. Your role will involve ensuring the highest quality and timely delivery of data, conducting quality control checks, and mentoring junior team members. Key Responsibilities: - Contribute to projects such as Targeted Literature Reviews (TLR), Systematic Literature Reviews (SLR), Value Dossiers (GVD), and Scientific Publications - Ensure clear, complete, accurate, and concise presentation of data - Perform quality control checks and proofreading of assigned documents - Demonstrate excellent knowledge of systematic review methodology and HTAs submissions - Write market access documents like AMCP dossiers and GVD - Analyze and interpret data, including report writing - Take accountability for writing, reviewing, literature searches, and project management - Support business growth through client relationship development - Guide and mentor junior team members Qualifications: - Masters degree, PharmD, PhD, or equivalent in medicine/pharmacy - 3-6 years of experience in HEOR and medical writing domains - Knowledge of reference management software like EndNote/Reference Manager - Experience in conducting meta-analysis and network-meta-analyses (RevMan, STATA, R) - Proficiency in Microsoft Word, Excel, and PowerPoint Additional Skills: - Understanding of economic evaluation techniques and basic health economic modeling - Knowledge of real-world evidence studies and global market access environment - Strong time management, project management, and communication skills - Ability to interpret data, write reports, and make recommendations - Proactive problem-solving approach and willingness to learn and adapt - Experience in primary research or conducting workshops with key opinion leaders Company's Employee Value Proposition: - Inclusive environment encouraging diverse perspectives - Challenging opportunities to contribute to organizational success - Technical challenges impacting across geographies - Self-development opportunities through Axtria Institute, global knowledge sharing, and external certifications - Sponsored Tech Talks & Hackathons - Possibility to relocate for short and long-term projects Benefit Package: - Health benefits - Retirement benefits - Paid time off - Flexible Benefits - Hybrid/FT Office/Remote work options If interested, please share your profile with Deepika (deepika.biswas@axtria.com),

Role Overview: You will be responsible for leading the scientific manuscript publication process for JoVE's prestigious JoVE Journal. This role involves managing cross-functional teams to ensure the efficient delivery of a high volume of scientific publications. As a part of a rapidly growing company, you will play a crucial role in maintaining scientific rigor and editorial excellence across all published content. Key Responsibilities: - Lead and manage the JoVE Journal teams, including Peer Review Editors, Content Writers, and Video Production staff to ensure smooth publishing operations. - Oversee the complete manuscript workflow from peer review to publication, focusing on timeliness, quality, and adherence to journal standards. - Identify inefficiencies and process bottlenecks; implement continuous improvement initiatives to enhance throughput and reduce publication timelines. - Monitor industry trends and emerging technologies like AI to optimize workflows, enhance productivity, and improve the author experience. - Define team KPIs and departmental goals, monitoring performance and ensuring accountability. - Maintain scientific rigor and editorial excellence across all published content to align with JoVE's standards. - Identify new journal sections or special issues in response to emerging research trends. Qualifications Required: - A Masters or Ph.D. in life sciences. - 10+ years of experience in academic, scientific publishing, or edtech content production, with a specialization in managing publication workflows. - 7+ years of proven management experience. - Strong understanding of peer review, open access trends, and evolving scientific publishing models. - Experience with digital publishing technologies, Content Management System (CMS), and workflow automation tools. - Demonstrated experience in integrating technology and digital tools to improve publishing workflows, quality, and efficiency; familiarity with AI-based or automated solutions is a strong plus. - Exceptional attention to detail, with strong communication skills. - Self-starter with a results-driven mindset, thriving in a fast-paced environment. - Experience working in a global environment is a strong plus. Additional Details of the Company: JoVE is the world-leading producer and provider of science video solutions, dedicated to enhancing scientific research and education. With a diverse and international team, JoVE offers you the opportunity to make a direct impact in accelerating science research and improving student learning in science education. The company's strong promotion from within culture provides a clear path for advancing your career within JoVE.,

As a Scientific Writing - Project Specialist at Opella in Hyderabad, your role involves providing project management support to the scientific writer to ensure effective project delivery of designated publications/medical education deliverables. You will be responsible for initiating and amending submissions based on comments, supporting internal and external stakeholder communication, tracking delivery activities, managing issues and risks, ensuring compliance with publication processes, managing budgets, and tracking external spend. Key Responsibilities: - Support the scientific writer in end-to-end project delivery of designated publications/medical education deliverables - Initiate and amend submissions based on comments - Support internal and external stakeholder communication - Track delivery activities, manage issues and risks - Ensure compliance with publication processes and tools - Manage the assigned publication or medical education within the agreed budget - Track external spend and ensure compliance with associated activities and approvals - Collaborate with scientific communication global and/or local teams and medical content enhancement teams Qualifications Required: - Experience: 1-2 years post-qualification experience - Soft skills: Stakeholder management, communication skills, ability to work independently and within a team environment - Technical skills: Project management, Scientific/Medical writing/communications, experience in managing assets in tools like PromoMats, DAM, iEnvision & DataVision, Pharma experience - Education: University degree level (Graduate degree, preferably in science), relevant advanced/postgraduate degree in life sciences/pharmacy/similar discipline desirable - Languages: Excellent knowledge of spoken and written language In addition to your responsibilities, you will have the opportunity to work on challenging and purposeful projects at Opella. You will be part of a collaborative and inclusive culture where personal growth and development are encouraged. Join us in our mission to bring health into people's hands. Visit www.opella.com/en/careers to explore opportunities with us.,

As an Associate - Scientific Writing Omnichannel Marketing at Indegene, you will be responsible for leading the development of scientific and promotional content for pharmaceutical and healthcare brands. Your key responsibilities will include: - Content Development: - Drafting, reviewing, and editing scientific and promotional content for various channels. - Translating complex scientific/clinical data into clear and engaging messaging. - Preparing medical claims matrices and references to support content. - Research & Accuracy: - Conducting literature reviews and synthesizing findings into brand-relevant content. - Ensuring all materials are scientifically accurate and aligned with the source data. - Staying updated on therapeutic areas, clinical trial updates, and pharma industry trends. - Compliance & MLR Submissions: - Preparing and submitting content for approval through platforms like Veeva Promomats. - Incorporating Medical, Legal, and Regulatory feedback in a timely manner. - Ensuring all content meets FDA, HIPAA, and client-specific compliance standards. - Collaboration: - Working with medical reviewers, brand managers, and creative teams to ensure content quality. - Supporting omnichannel campaign teams in aligning content with brand strategies. Qualifications: - Experience: - 4-6 years as a scientific/medical content writer in the US pharmaceutical or healthcare industry. - Experience in developing content across digital and omnichannel formats. - Hands-on experience with Veeva Promomats or similar MLR platforms. - Skills: - Strong ability to interpret and simplify scientific/clinical data. - Excellent writing, editing, and attention to detail. - Knowledge of referencing styles and medical literature review. - Ability to work effectively in cross-functional and regulatory-driven environments. - Education: - Bachelors/Masters degree in Life Sciences, Pharmacy, Medicine, or related field. - Training or certification in medical/scientific writing is an advantage. Indegene is a technology-led healthcare solutions provider with a purpose to enable healthcare organizations to be future-ready. They offer accelerated global growth opportunities for individuals who are bold, industrious, and nimble. At Indegene, you will experience a career guided by passion, innovation, collaboration, and empathy. Join Indegene to work at the exciting intersection of healthcare and technology and be mentored by industry experts for a differentiated career journey.,

Job Description: As a Medical-Regulatory Writer Assistant Manager, your main responsibility will be to plan and manage Medico-Regulatory Writing in accordance with relevant Regulatory Guidelines. You will be expected to deliver high-quality medical and scientific writing, provide technical consultation and advice on strategy and regulations, demonstrate subject matter expertise, effectively manage writing projects to meet deadlines, collaborate with internal and external clients, and produce various types of reports including CTD Modules, Safety Reports, and Aggregate Reports. Key Responsibilities: - Conduct science reviews of aggregate reports - Ensure document compliance with client specifications - Attend project meetings - Stay updated on regulatory guidance - Maintain Aggregate Report Tracker - Perform detailed searches on regulatory agency websites - Mentor associates - Provide effective communication for operational excellence Qualifications Required: - Master's degree in Pharmacology/Pharmacy/Medicine with a minimum of 5 years of experience - Advanced degree preferred - Previous experience in the pharmaceutical/CRO industry - Additional qualifications in medical writing (AMWA, EMWA, RAC) would be advantageous,

As an experienced and motivated Adjunct Faculty member with a strong background in medicine, nutrition, or related life sciences, your role will involve supporting content development and academic writing. This fully remote position offers flexibility while contributing to the creation of high-quality educational materials, research summaries, and scientific communications. Ideally suited for fresh MBBS graduates preparing for their MD, PhD students, or fresh PhDs in specialities listed below in qualifications. **Key Responsibilities:** - Develop educational content for courses, workshops, and publications in the fields of nutrition, exercise science, molecular biology, and allied health. - Write, edit, and review scholarly articles, research summaries, and academic materials. - Ensure scientific accuracy, clarity, and adherence to academic standards in all written materials. - Collaborate virtually with faculty, researchers, and instructional teams to translate complex concepts into accessible content. - Stay updated with recent research and advances in relevant fields to inform content creation. **Required Qualifications:** - MBBS. - MD specialities - Path, Internal Medicine, OB-GYN, Paediatrics, Family Medicine, Preventive Healthcare, Community Medicine, Physical Therapy, Sports Medicine, Public Health, Endocrinology. - PhD in Nutrition, Exercise Science, or related discipline. - Proven track record of academic publications in peer-reviewed journals. - Demonstrated experience in academic writing, scientific communication, or content development. - Strong command of scientific writing standards, referencing, and ethical research reporting. **Preferred Skills:** - Experience in curriculum or educational content development. - Ability to simplify complex scientific concepts for diverse audiences. - Familiarity with digital content tools and platforms for academic publishing. In addition to the above, there are multiple positions available for this fully remote role, offering flexibility in work location and hours. If you are interested and suitable for the role, please send your resume and cover letter to career@fittr.com with the subject line: Application for (Position Name) (Your Name).,

As a Medical Writer - Manager, your role is crucial in driving and translating creative and contemporary ideas into impactful designs. You will be responsible for designing and deploying creative campaigns for global clients, including Fortune 50 companies. In this role, your key responsibilities will include: - Writing clear, engaging, and medically accurate content for various audiences such as press materials, consumer campaigns, digital assets, and educational tools. - Translating complex clinical and scientific information into language that resonates with non-specialist audiences like patients, caregivers, and media outlets. - Developing messaging that aligns with brand strategy while simplifying technical data for broader understanding without compromising accuracy. - Partnering with internal teams (account, strategy, and creative) to ideate and execute content that is impactful, on-brand, and compliant. - Revising and refining copy based on internal and client feedback as well as MLR reviewer input. You will collaborate closely with our global creative agency teams and work with a team of talented designers to deliver high-quality services. Qualifications required for this role: - 11+ years of experience in healthcare communications agencies (AMA experience preferred). - Bachelor's degree or equivalent experience with a focus on pharma/science/medicine. - Portfolio containing work samples demonstrating medical writing for various communication forms (e.g., sales aids, direct mail, websites, social media) for diverse audiences (e.g., healthcare professionals, patients, consumers). - Knowledge of the AMA Style Guide (certification not mandatory). - Experience with referencing, annotating, and client MLR submissions requirements. - Ability to understand and process healthcare information. - Ability to multitask in a fast-paced environment as a member of a highly collaborative team. - Desire to work with diverse teams, projects, and clients. - Strong conceptual ability, creative thinking, and exceptional writing skills. Join us as we continue to grow rapidly and provide stellar products and services in various areas. Let's build this together!,

As a Scientific Officer at the American Board of Education (ABE) in Kochi, Kerala, India, your primary role will involve coordinating and overseeing scientific research projects, supporting curriculum development, and providing guidance in related disciplines. You will be responsible for conducting and publishing research, advising on academic initiatives, and collaborating with educational institutions to enhance teaching strategies and student outcomes. **Key Responsibilities:** - Coordinate and oversee scientific research projects - Support curriculum development efforts - Provide guidance in related disciplines - Conduct and publish research in scientific fields - Advise on academic initiatives - Collaborate with educational institutions to enhance teaching strategies and student outcomes **Qualifications Required:** - PhD in any discipline - Outstanding English communication skills for writing, editing, and presentations - Strong analytical, organizational, and time-management skills - Proficiency with research tools, referencing styles, and MS/Google productivity suites - Experience in curriculum development is a plus - Experience in University Teaching and Research is a plus The American Board of Education (ABE) is a U.S.-based non-profit organization committed to accrediting post-secondary institutions and career colleges globally. Headquartered in Los Angeles, California, ABE evaluates academic quality, instructional delivery, and student outcomes, while supporting partner institutions in curriculum development and standardized program delivery. ABE certifies individual competencies through rigorous examinations and awards globally recognized professional credentials. In addition to accreditation, ABE provides strategic advisory services to enhance institutional performance and academic innovation. ABE's flagship School Research Program nurtures early talent, guiding students from grade eight to develop research skills and publish in international journals. To apply for this position, please email your resume (and a brief cover note) to careers@educationboard.us with the subject line "Scientific Officer - Kochi". Preferred Start Date: ASAP Compensation: Competitive; commensurate with experience EEO: The American Board of Education (ABE) is an equal opportunity employer.,

As an Editorial Language Editor specializing in Life Sciences and Medical Writing, you will play a crucial role in ensuring the clarity, accuracy, and publication readiness of academic manuscripts, research papers, and scientific content for global scientific and medical journals. Your responsibilities will include: - Performing comprehensive language editing of manuscripts in life sciences, medicine, biotechnology, and related fields. - Ensuring that scientific content is clear, concise, and coherent, while adhering to journal-specific guidelines and formatting requirements. - Editing for grammar, punctuation, style, tone, syntax, and consistency, maintaining the authors" original intent. - Conducting structural and substantive editing, including sentence-level rewrites to enhance logical flow and clarity. - Collaborating with in-house editorial, quality assurance, and production teams to deliver high-quality content. - Researching and integrating subject-specific terminology to uphold scientific accuracy. - Providing constructive feedback to authors for improving content quality and structure. - Ensuring timely delivery of edited content while upholding quality benchmarks and meeting tight turnaround timelines. Your must-have competencies include: - Excellent command of written and spoken English with the ability to simplify complex scientific language. - Hands-on experience in academic and scientific editing within life sciences, medicine, biotechnology, or pharmaceuticals. - Proficiency in MS Office tools such as Word, Excel, and PowerPoint. - Strong attention to detail, organizational skills, and multitasking abilities. - Capability to work independently and meet deadlines in a fast-paced editorial environment. - Familiarity with scientific publishing standards, referencing styles (APA, MLA, Vancouver, etc.), and peer-reviewed journal requirements. Preferred qualifications for this role consist of: - Experience in medical/scientific writing or editing for publishers, CROs, or academic institutions. - Knowledge of editorial workflows, QA processes, and handling author queries. - Recognition or certifications in editing or writing from reputable bodies (e.g., IGMPI, AMWA, BELS). - Previous involvement in freelance, contract, or full-time editorial positions for medical journals, life sciences publications, or educational content platforms. In terms of educational requirements, a Ph.D. or Masters Degree in Life Sciences, Biochemistry, Biotechnology, or related fields is preferred. A Bachelor's degree in Medical Laboratory Technology or an equivalent clinical/scientific degree would be an added advantage. Certifications in medical writing or scientific editing (e.g., Executive Diploma in Medical Writing) are also desirable. Your key soft skills should include: - Strong interpersonal and communication skills. - Team player mindset with a keen eye for detail. - Excellent time management and prioritization abilities. By joining this purpose-driven editorial team, you will have the opportunity to work on impactful global content within the scientific and healthcare domains. You will be part of an organization that values quality, precision, continuous learning, and collaboration with renowned authors and researchers.,

Role Overview: As a Scientific Writer at the company, you will be responsible for providing high-quality writing support and project management of scientific communication projects in compliance with good publication practices. Your role will involve translating complex clinical data into clear and accessible content tailored to healthcare professionals (HCPs), patients, and other stakeholders both external and internal. Key Responsibilities: - Possess the ability to understand a therapeutic area and product strategy to ensure scientific communication objectives are met. - Learn quickly to understand a new therapeutic area and adapt work across multiple therapeutic areas. - Translate complex scientific information and clinical trial data into content that meets the needs of various audiences, including HCPs and patients. - Write key scientific communication deliverables such as abstracts, posters/presentations, and manuscripts. - Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure global content is relevant, up-to-date, and aligned with evolving data. - Maintain robust version control and document tracking to ensure transparency, audit-readiness, and traceability in Teva's publication tracking tool. - Establish relationships with authors, external experts, and clinical trial investigators to ensure efficient development of high-quality publications. - Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams to gain input and approval of scientific communication deliverables. - Follow Good Publication Practices and internal SOPs to ensure consistency and compliance. - Conduct peer reviews of content developed by other writers to uphold high-quality standards. - Participate in initiatives to enhance the content development process, including the use of AI tools, structured content libraries, and digital asset management systems. - Support the development of derivative content assets such as field medical affairs materials, congress preparation content, and other digital assets. Qualifications Required: - Education: Advanced degree (PharmD, PhD, MD, or Masters in Life Sciences or related field) required. - Language: English (Professional level competency) - Experience: 10-12 years of experience in medical writing, medical information, or scientific communications within the pharmaceutical, biotech, or medical device industry. - Experience with medical publication writing, scientific literature analysis, and congress content preparation. - Knowledge of Good Publication Practices and ICMJE Guidelines. - Familiarity with publication management systems (e.g., Datavision, Pubstrat, Komodo) and publication workflows. Role Overview: As a Scientific Writer at the company, you will be responsible for providing high-quality writing support and project management of scientific communication projects in compliance with good publication practices. Your role will involve translating complex clinical data into clear and accessible content tailored to healthcare professionals (HCPs), patients, and other stakeholders both external and internal. Key Responsibilities: - Possess the ability to understand a therapeutic area and product strategy to ensure scientific communication objectives are met. - Learn quickly to understand a new therapeutic area and adapt work across multiple therapeutic areas. - Translate complex scientific information and clinical trial data into content that meets the needs of various audiences, including HCPs and patients. - Write key scientific communication deliverables such as abstracts, posters/presentations, and manuscripts. - Collaborate with Scientific Communication Leads and Therapeutic Area Leads to ensure global content is relevant, up-to-date, and aligned with evolving data. - Maintain robust version control and document tracking to ensure transparency, audit-readiness, and traceability in Teva's publication tracking tool. - Establish relationships with authors, external experts, and clinical trial investigators to ensure efficient development of high-quality publications. - Work cross-functionally with Medical Affairs, Clinical Development, Safety, and other teams to gain input and approval of scientific communication deliverables. - Follow Good Publication Practices and internal SOPs to ensure consistency and compliance. - Conduct peer reviews of content developed by other writers to uphold high-quality standards. - Participate in initiatives to enhance the content development process, including the use of AI tools, structured content libraries, and digital asset management systems. - Support the development of derivative content assets such as field medical affairs materials, congress preparation content, and other digital assets. Qualifications Required: - Education: Advanced degree (PharmD, PhD, MD, or Masters in Life Sciences or related field) required. - Language: English (Professional level competency) - Experience:

As the Scientific Communications MLR Technical Reviewer at the company, your role involves checking all medical content for data and scientific accuracy, and reference appropriateness for materials submitted through the Medical, Legal, and Regulatory (MLR) process. It is your responsibility to ensure that all content aligns with Amgen's scientific and compliance standards, facilitating timely review and approval of assets that educate and engage healthcare providers, patients, and internal stakeholders. Working in collaboration with the US Scientific Communications MLR Reviewer, your scientific expertise, attention to detail, and compliance awareness play a crucial role in evaluating submissions and maintaining the quality and consistency of Amgen's communications. **Roles & Responsibilities:** - Conduct a review of proactive materials for scientific accuracy and reference appropriateness - Review the material to ensure appropriate medical context, scientific balance, and compliance are maintained - Ensure timely and high-quality review of MLR materials within established SLAs and agreed-upon timeframes - Collaborate with the US Scientific Communication MLR Reviewer to provide clear guidance on action items - Work within Amgen's MLR systems to apply clear review comments per company process - Conduct and participate in knowledge-sharing sessions to align on therapeutic areas, products, and review best practices - Provide scientific guidance to cross-functional teams regarding appropriate interpretation and use of data in promotional and medical content - Support standardization of review practices, templates, and criteria to enhance efficiency and consistency across reviews - Stay current on therapeutic area developments, industry guidelines, and regulatory requirements relevant to MLR reviews - Contribute to process improvement initiatives and adoption of new technologies that enhance review workflows **Basic Qualifications and Experience:** - Doctorate degree & 2 years of directly related experience OR - MBBS or Masters degree & 4 years of directly related industry experience OR - Bachelors degree & 4 years of directly related industry experience OR - Associates degree & 6 years of directly related industry experience **Functional Skills:** - Doctorate degree in life sciences, pharmacy, biomedical sciences, or a related field - 5+ years of experience in medical review, medical writing, scientific communications, publications, or related industry role - Familiarity with the MLR review process and regulatory requirements for medical and promotional materials - Strong ability to critically evaluate data, references, and claims for scientific accuracy and compliance - Prior experience with content management and MLR review systems (e.g., Veeva PromoMats or equivalent) - Excellent attention to detail and organizational skills to manage multiple, concurrent submissions under tight timelines - Strong written and verbal communication skills to interact effectively with cross-functional stakeholders - Knowledge of therapeutic areas such as oncology, cardiovascular, inflammation, bone, and rare diseases is a plus - Understanding of US compliance, copyright, and transfer-of-value requirements **Competencies:** - Scientific Integrity: Upholds rigorous standards in data accuracy and interpretation - Collaboration: Works effectively with cross-functional global teams in MLR review cycles - Attention to Detail: Ensures consistency, accuracy, and compliance in content review - Time Management: Prioritizes high-volume review workload and meets critical deadlines - Adaptability: Adjusts to evolving review practices, systems, and regulatory expectations - Compliance: Demonstrates commitment to integrity in all aspects of review work Please note that the company is committed to providing reasonable accommodations for individuals with disabilities during the job application, interview process, essential job functions, and other benefits and privileges of employment. Feel free to reach out to request accommodation if needed.,

Role Overview: As an Associate Scientific Director at Red Nucleus, you will be a key member of the Medical Communications team. Your role will involve leading scientific accounts, providing high-quality editorial review, and acting as a scientific and therapeutic expert for assigned project teams. You will set standards for content development, mentor medical writing staff, and support business development efforts. Key Responsibilities: - Set standards for the assigned team to drive continuous improvement in quality and client interactions - Evaluate internal processes related to content development and suggest improvements - Ensure high-quality outputs from the scientific team - Identify training needs within the team, develop plans, and oversee implementation - Lead medical writers to develop clear and accurate content - Provide medical direction and develop strategy for clients" medical/scientific communications programs - Interact with external thought leaders, client colleagues, and clinical leads - Cultivate expertise in assigned therapeutic areas - Work closely with Client Services to ensure projects are resourced, completed on time, and within budget - Oversee medical writer recruitment for assigned account(s) - Identify opportunities for account growth and participate in client discussions - Assist new/junior writers with content development and serve as a resource - Comply with editorial procedures and ethical standards - Represent the company at client meetings in a professional manner Qualifications Required: - PhD in a biomedical science/PharmD/MD preferred - Minimum of 4 years of experience in medical communications as a medical writer - Experience mentoring junior writers - Knowledge of scientific and regulatory requirements for clinical studies - Excellent communication, leadership, and organizational skills - Familiarity with GPP and ICMJE guidelines - CMPP preferredAbility to travel (Note: The additional details about the company and employee benefits have been omitted as they were not explicitly mentioned in the job description),

As a Medical Communications Associate at Novartis, you will work in partnership with the Client Engagement team, Medical Communications, and the Writing delivery team for a designated client group/therapeutic area (TA)/brand. Your responsibilities will include: - Ensuring medical communications deliverables are aligned with assigned scientific goals and objectives. - Ensuring written materials contain appropriate scientific statements and support learning objectives. - Developing original content, leading faculty and client communications relating to scientific content of medical communications deliverables. - Ensuring quality, scientific accuracy, and integrity of assigned projects. - Assisting the client to achieve medical communication objectives through the creation and execution of scientific and educational materials. - Training and mentoring the Writing delivery teams on selected therapy areas. Your key responsibilities will involve: - Supporting the planning and execution of scientific communications for assigned franchises/TA or group of aligned TAs. - Overseeing the delivery of client-requested support of medical/scientific communications plans and medical communications workshops for assigned franchises/TA or group of aligned TAs. - Leading the review of the medical/scientific communication plans with stakeholders to ensure their requirements are met. - Collaborating with Content Development - US Medical Affairs in developing plans and materials for new business development meetings with existing and prospective clients. - Demonstrating the ability to think creatively and applying extensive knowledge of assigned franchises/TA or group of aligned TAs. - Maintaining thorough knowledge of key competitors and recommending strategy-aligned medical communications solutions to meet client needs. Additionally, you will be responsible for: - Overseeing medical communication content development for high-profile and scientifically complex therapeutic areas. - Ensuring the quality and scientific accuracy/integrity of projects. - Providing guidance and direction to writers/editorial project team. - Detecting/anticipating strategic inconsistencies or potential problems and developing solutions. - Leading by example in terms of working with the client and championing optimum collaboration between Content Development - US Medical Affairs and the internal client. Qualifications required: - Education: Healthcare professional degree or degree in a healthcare-related field. - Desirable: Advanced degree (PhD, PharmD, MD) in life science/healthcare. Experience: - At least 5 years of experience working with international Medical Communications for either an agency or in an internal role within the pharmaceuticals industry. - Experience in various Medical Communications activities, including publications, slide decks, symposia, standalones, advisory board meetings, etc. - Track record in developing Medical Communications plans. - Desired experience in digital solutions and innovation. - Experience in a multi-cultural work environment and international working. In addition to the above, Novartis is committed to diversity and inclusion. Join our Novartis Network to stay connected and learn about suitable career opportunities. Novartis offers benefits and rewards to help you thrive personally and professionally. At Novartis, we are dedicated to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.,

You will be joining VyasLife, a rapidly expanding startup in the healthcare technology and services sector, as a Team Lead in Medical Writing. Your role will involve using your scientific knowledge to create accurate and informative content, providing leadership and mentorship to a team of medical writers, collaborating with cross-functional teams, managing multiple projects simultaneously, and enhancing the team's writing skills and knowledge of medical and scientific concepts. - Effectively create accurate, informative, and precise content that adheres to technical specifications - Provide leadership, guidance, and mentorship to a team of medical writers, setting clear objectives, goals, and priorities - Collaborate with cross-functional teams to align on content requirements and timelines - Manage multiple projects simultaneously, ensuring timely completion and adherence to deadlines - Conduct skill development sessions to enhance the team's writing skills and knowledge of medical and scientific concepts - Possess effective presentation, proofreading, and interpersonal skills with a team-oriented approach - Interpret and present clinical data and other complex information based on principles of clinical research - Life-sciences graduate with a master's or PhD degree - 5 to 7 years of proven experience in medical writing within the pharmaceutical, biotech, or healthcare industries - Strong leadership and managerial skills with the ability to motivate the team - Excellent oral and written English communication skills - Superb English writing and editing skills with attention to detail - In-depth knowledge of medical terminology, clinical research, and regulatory requirements,

As a Scientific Communications Associate Project Manager at Amgen, your role involves providing project management support across the Scientific Communications portfolio, including publications, medical content, and congress deliverables. You will work in alignment with business priorities, quality standards, and compliance requirements. Your responsibilities include managing stakeholder communication, tracking activities, timelines, ensuring compliance with Amgen's Scientific Communications processes, and collaborating with global and local teams for timely, accurate, and compliant project delivery. **Roles & Responsibilities:** - Planning and managing end-to-end project schedules, scope, dependencies, and deliverables for publications, medical content, and congress activities - Facilitating team meetings, capturing decisions and action items, and driving timely follow-through - Supporting in building dashboards and routine reports to monitor data quality, assess impact, and communicate KPIs and compliance measures - Coordinating congress planning and execution support in alignment with established processes - Supporting in the end-to-end management of publication or other scientific communications deliverables - Supporting publications operations in partnership with US-based publication planners and subject matter experts - Driving continuous improvement by identifying process inefficiencies and opportunities for automation, contributing to user acceptance testing, and training for adoption of new tools - Ensuring adherence to Amgen Standard Operating Procedures (SOPs), quality standards, and regulatory requirements **Basic Qualifications and Experience:** - Masters degree in life sciences/pharmacy/MBA/similar discipline OR - Bachelors degree in life sciences/pharmacy/MBA/similar discipline & 1.5 years of directly related industry experience OR - Associates degree & 3 years of directly related industry experience **Preferred Qualifications:** - 3+ years of project management experience leading cross-functional initiatives, preferably in a regulated, compliance-driven environment - Working experience in publications, scientific writing, or scientific communications processes - Working knowledge of common biotech platforms, such as Salesforce and Veeva Vault - Knowledge of publication submission process, congresses, and tools - Proficiency with modern productivity and collaboration tools (e.g., Microsoft 365, SharePoint, Miro) and MS Planner or similarly structured project management applications - Strong written and verbal communication skills; proven experience facilitating meetings, summarizing decisions, and producing clear status updates - Exposure to automation and AI-assisted workflows to streamline processes and improve quality - Ability to work independently and within a team environment - Ability to work effectively across time zones and in a highly matrixed organization At Amgen, we prioritize providing reasonable accommodation to individuals with disabilities throughout the job application, interview process, essential job functions, and other benefits of employment. Feel free to contact us to request an accommodation.,

Role Overview: As a Medical Writer II (Narrative Writing) at Syneos Health, you will be part of a leading fully integrated biopharmaceutical solutions organization focused on accelerating customer success. Your main responsibility will be to compile, write, edit, and coordinate medical writing deliverables that present scientific information clearly and accurately. You will work as a medical writer within and across departments with minimal or moderate supervision. Your role will involve completing various documents such as clinical study protocols, clinical study reports, patient narratives, annual reports, and more. You will adhere to established regulatory standards and ensure timely completion of medical writing projects within budget. Key Responsibilities: - Main experience in CSR safety narratives writing including authoring, addressing review comments, and collaborating with teams. - Compilie, write, edit, and coordinate medical writing deliverables that present scientific information clearly and accurately. - Complete a variety of documents including clinical study protocols, patient narratives, annual reports, and more. - Adhere to established regulatory standards, company standard operating procedures, and client standards when completing medical writing projects. - Coordinate quality and editorial reviews, lead document reviews, and resolve comments from clients. - Interact and build good working relations with clients, department heads, and peers to produce writing deliverables. - Perform online clinical literature searches and comply with copyright requirements. - Mentor less experienced medical writers on projects as necessary. - Maintain a strong working knowledge of drug development process, regulatory guidelines, and industry standards. - Work within budgeted hours and communicate status and changes to medical writing leadership. Qualifications Required: - Bachelor's degree in a relevant discipline with relevant writing experience; graduate degree preferred. - At least 2 years of relevant experience in science, technical, or medical writing. - Experience working in the biopharmaceutical, device, or contract research organization industry preferred. - Familiarity with FDA and ICH regulations, other regulatory guidelines, and good publication practices strongly preferred. - Extensive knowledge of English grammar and ability to communicate clearly; familiar with AMA Manual of Style. (Note: The above qualifications mentioned are as per the Job Description provided. Any equivalent experience, skills, and education may also be considered.),

As an Expert Scientific Writer at Novartis Healthcare Private Limited in Hyderabad, your primary responsibility will be to manage and complete various Medical Communications deliverables with high quality standards and within agreed timelines. Your projects will include manuscripts, abstracts, posters, slide sets, satellite symposia content, congress or advisory board reports, publication planning, and medical education materials for internal medical and/or clinical teams. Key Responsibilities: - Demonstrate a command of assigned therapeutic areas and expertise with assigned products - Research and write original content for various publications activities - Prepare meeting materials for satellite symposia and reports from advisory boards - Perform quality control checking and proofreading of documents - Clearly communicate medical scientific concepts in a condensed, audience-appropriate way - Interpret and apply clinical data in medical communication deliverables - Develop and adhere to logical and attainable timelines for project completion - Lead and/or participate in author/client teleconferences - Provide accurate citations in text and bibliography for medical review - Participate in strategic and tactical publications planning Qualifications Required: - Minimum science degree or equivalent education - Desirable: MSc, PhD, PharmD, or MD - Minimum of 5 years of experience in medical communications - Medical writing experience - Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) As part of the Novartis team, you will play a crucial role in reimagining medicine to improve and extend people's lives. Novartis is committed to creating an inclusive work environment and diverse teams that are representative of the patients and communities served. If you are looking to be part of a community of smart, passionate individuals dedicated to making a difference in patients" lives, then join our mission at Novartis. For more information about benefits and rewards, you can refer to the Novartis Life Handbook available at: [Novartis Life Handbook](https://www.novartis.com/careers/benefits-rewards). Novartis is dedicated to providing reasonable accommodations to individuals with disabilities. If you require accommodation during the recruitment process, please contact [email protected] with your request and contact information, mentioning the job requisition number in your message. Join the Novartis Network to stay connected and learn about suitable career opportunities in the future: [Novartis Network](https://talentnetwork.novartis.com/network).,