3,501 Medical Research Jobs in Chengalpattu

Role Overview: As the Primary scientific face of the organization to Thought Leaders & physicians for a given therapy area at Dr. Reddys Laboratories Ltd., your main responsibility will be the Identification, mapping, and profiling of thought leaders in a given geography and therapy area on an ongoing basis. Key Responsibilities: - Engage identified key thought leaders through medical affairs activities in alignment with the overall strategic plan. - Execute strategic medical affairs plans including medical education, product education, medical evidence generation, advisory boards, pre-license activities, and special projects. - Act as a therapeutic area scientific expert to discuss scientific data, patients treatment trends, and studies in the relevant therapeutic areas with leading specialists. - Support optimal patient outcomes through effective communication of data, information, knowledge, and insights. - Represent the organization in various internal and external scientific platforms. - Gather deep insights on disease trends and treatment patterns from key thought leaders and convey them back to therapy lead and commercial teams. - Proactively conduct disease trend analysis and contribute to the development of the annual Medical Affairs Strategy Plan. - Receive and process scientific information requests from physicians. - Ensure all activities are conducted in alignment with the organization's COBE (Code of Business Ethics) Policy and compliance guidelines. - Collaborate with thought leaders to conduct therapy-specific reviews, meta-analysis, case studies, and publish them in reputable journals. - Devise optimal training plans to keep sales and marketing teams updated with the latest medical developments. - Develop Medical Affairs strategic plans for identified therapeutic areas and products. - Identify knowledge, practice, and data gaps, and develop strategic medical action plans. - Handle complex questions from healthcare professionals related to products or disease areas satisfactorily. - Ensure promotional, physician, and patient education materials are approved within stipulated timelines and in alignment with the organization's policies. - Identify unmet needs through stakeholder interactions and contribute to new product ideation and development. Qualification Required: - Educational Qualification: MBBS with a full-time post-graduate qualification of at least 2-years duration in any discipline of medicine or M.B.B.S with M.B.A. from a reputed institute. - Minimum work experience: Fresh postgraduate or up to 2 years of experience in Field-based Medical Affairs. Additional Details (if present): Dr. Reddys Laboratories Ltd. is a leading multinational pharmaceutical company committed to accelerating access to affordable and innovative medicines. With a focus on deep science, progressive people practices, and robust corporate governance, the company aims to reach over 1.5 billion patients worldwide by 2030. Dr. Reddys fosters a culture of empathy and dynamism, where individuals are supported in a collaborative environment to make a difference in healthcare.,

Role Overview: As an MBBS/MD, your primary responsibility will be to write brief case report types of questions (MCQs) with detailed explanations for all the options. These questions should be prepared on various medicine exams/MBBS subjects. You are expected to work remotely from home for 20-25 hours per week and commit to a two-year duration. Key Responsibilities: - Create brief case report types of MCQs with detailed explanations for all options - Ensure the questions are based on various medicine exams/MBBS subjects - Maintain a high level of technical accuracy and avoid factual errors - Produce plagiarism-free content - Demonstrate excellent writing abilities and attention to detail - Collaborate effectively with editors and team leads - Follow in-house guidelines and style guide strictly Qualifications Required: - Minimum 5 years of experience in educational content creation - Experience in US medical board exam/question writing is a plus - Proficiency in writing on all MBBS subjects - History of association with a professional company - At least 5 published articles in reputable international journals - Strong motivation and goal-oriented mindset - Ability to work well in a team environment - Submission of a cover letter explaining why you are the best candidate for the job - Submission of a professional and complete CV/resume - Submission of published international articles Please note that BDS/MDS candidates are not eligible for this position. Only serious candidates meeting the above criteria should apply for this remote work opportunity.,

Role Overview: You will be joining NovoBliss Research as a Clinical Investigator for the Research Unit based in Ahmedabad. Your main responsibilities will include assisting in medical research, conducting and managing medicine-related tasks, overseeing clinical trials, and contributing to the development of study designs for various product categories. Key Responsibilities: - Assist in medical research and conduct clinical trials - Manage medicine-related tasks effectively - Utilize and oversee clinical trials for various products - Contribute to the development and implementation of robust study designs Qualifications Required: - BDS, MDS, BAMS or Pharm D degree - Experience in conducting research and clinical trials - Proficiency in medicine-related tasks - Strong understanding of medical terminology - Attention to detail and accuracy in data management - Knowledge of regulatory requirements in clinical research - Bachelor's degree in Medicine, Clinical Research, or related field - Certification in Clinical Research would be beneficial,

Role Overview: As a Medical Officer at Modern Homeopathy Pvt. Ltd. in Nashik, your primary responsibility will be to lead the medical team and oversee healthcare services. You will play a crucial role as a clinical advisor, manage clinical trials, and ensure exceptional standards of inpatient care. Your contribution to patient care and dedication to maintaining the highest standards of healthcare services will be essential in this role. Key Responsibilities: - Contribute clinical expertise to patient care - Supervise junior physicians - Handle administrative duties and risk management - Ensure the highest standards of patient care are met - Verify complex diagnoses and assist in treatment plans - Recruit, supervise, and mentor healthcare professionals - Collaborate with consultants - Manage allocated budgets - Identify areas for improvement in inpatient care - Stay updated on field advancements - Participate in medical research programs - Ensure compliance with healthcare regulations and safety standards - Maintain accurate medical records - Act as a liaison between administrative and medical staff Qualifications Required: - BHMS qualification - Freshers and experienced individuals are welcome - Passion for making a difference in healthcare Please feel free to apply for this position by contacting us at +91 8956611981 or via email at headhr@modernhomeopathy.com.,

BHMS Provides understanding of patient care, medical terminology, and clinical documentation useful for data analysis and research. BDS Strong medical foundation; suitable for analyzing clinical or dental research data and quality improvement metrics. BMS (Biomedical) Excellent fit offers scientific and analytical training directly relevant to healthcare data analysis. JD Valuable if focusing on healthcare compliance, legal risk analysis, or policy/regulatory data analytics.

Please Note:This opportunity is for overseas placement only!This job is strictly for abroad placements, not for positions within India.Call & WhatsApp: Ms. Pallavi Singh 96-435-99936   Major Roles & Responsibilities   Accounts for coding and abstracting of patient encounters, including diagnostic and procedural information, significant reportable elements, and complications.Researches and analyzes data needs for reimbursement.Analyzes medical records and identifies documentation deficiencies.Serves as a resource and subject matter expert to other coding staff.Reviews and verifies documentation supports diagnoses, procedures and treatment results.Identifies diagnostic and procedural information.Audits clinical documentation and coded data to validate documentation supports services rendered for reimbursement and reporting purposes.Assigns codes for reimbursements, research and compliance with regulatory requirements utilizing guidelines.Follows coding conventions. Serves as coding consultant to care providers.Identifies discrepancies, potential quality of care, and billing issues.Researches, analyzes, recommends, and facilitates a plan of action to correct discrepancies and prevent future coding errors.Identifies reportable elements, complications, and other procedures.Serves as a resource and subject matter expert to other coding staff.Assists lead or supervisor in orienting, training, and mentoring staff.Provides ongoing training to staff as needed.Handles special projects as requested.  

As a skilled Promotional Medical Content Writer/Medical copywriter, you will be responsible for developing high-quality, engaging, and compliant medical content for omnichannel pharmaceutical marketing. Your expertise in crafting content for both healthcare professionals (HCPs) and patients across various platforms, including digital, print, social media, email campaigns, and sales enablement materials, will be crucial. You will need to blend scientific accuracy with creative storytelling to enhance brand messaging, drive engagement, and ensure regulatory compliance. Key Responsibilities: - Create compelling, evidence-based promotional content for HCPs and patients across multiple channels such as websites, eDetailers, webinars, emails, social media, brochures, and videos. - Translate complex scientific and clinical data into clear, engaging, and persuasive messaging tailored to different audiences. - Align content with brand strategy, medical positioning, and omnichannel marketing goals. - Develop SEO-optimized medical content for digital platforms like websites, blogs, and online portals. - Collaborate with marketing and creative teams to produce interactive content for omnichannel campaigns such as eDetailing, mobile apps, AI-driven chatbots, and virtual events. - Assist in developing personalized content journeys based on audience segmentation. - Ensure all content adheres to regulatory and compliance requirements (FDA, EMA, PhRMA, etc.). - Work closely with Medical, Legal, and Regulatory (MLR) teams to gain approvals for promotional materials. - Maintain accuracy in referencing scientific literature and clinical guidelines. - Collaborate with Medical Affairs, Brand, and Sales teams to align messaging with medical and commercial objectives. - Partner with designers, UX teams, and digital marketers to enhance content delivery. - Monitor content engagement metrics and adapt strategies based on insights. - Continuously update materials based on new scientific data, market trends, and HCP/patient feedback. Key Qualifications & Skills: - Educational Background: Bachelor's or Master's degree in Life Sciences, Pharmacy, Medicine, or Journalism with a medical writing focus. An advanced degree (PhD, PharmD, MD) is a plus. - Experience: 5+ years in medical content writing for pharma marketing, healthcare communications, or healthcare advertising agency. Experience in HCP and patient-focused content creation for omnichannel marketing. Knowledge of therapeutic areas like cardiology, endocrinology, oncology, or rare diseases is an advantage. Exposure to global markets (US/EU markets and their approval processes) will be a plus. - Technical & Soft Skills: Strong understanding of clinical research, scientific writing, and pharma promotional guidelines. Proficiency in English spoken and written is a must. Ability to simplify complex medical concepts for non-specialist audiences. Familiarity with SEO, UX writing, social media marketing, and email automation. Experience using content management systems (CMS), CRM platforms (Veeva, Salesforce), and analytics tools. Excellent project management, collaboration, and adaptability in fast-paced environments.,

As a Freelance Specialist Medical Writer and Editor at Pepgra, you play a crucial role in ensuring client satisfaction by producing high-quality research and evidence-based policy documents for publication in prestigious journals and regulatory submissions across various subject areas. Currently, we are seeking specialized freelance medical and clinical writers in Orthopaedics, particularly skilled in handling a wide range of disorders like Osteoarthritis, Rheumatoid Arthritis, Cubital Tunnel Syndrome, Carpal Tunnel Syndrome, Lateral Epicondylitis, and Medial Epicondylitis. Proficiency in English is essential, preferably as a first language (e.g., USA, Europe, UK), to collaborate with us on clinical research, writing, and editing projects. **Role Overview:** - Scientific research and writing in Orthopaedics involving writing, editing, proofreading, and peer-reviewing various manuscripts and clinical documents. - Adherence to job-specific instructions and working within set deadlines. - Conducting research on industry-related topics and delivering plagiarism-free content. - Ensuring correctness in content, terminology, flow, transition, and coherence. **Key Responsibilities:** - Hold a Post Doc/PhD/Master's degree or expertise in Orthopedics. - Possess research/writing experience and certification in academic writing, editing, publishing, and scientific communication. - Familiarity with different styles and conventions in academic and scientific writing. - Excellent writing and editing skills with keen attention to detail. **Qualifications Required:** - Post Doc/PhD/Master's degree in Orthopedics. - Research/writing experience with certification in academic writing and editing. - Knowledge of academic and scientific writing styles. - Strong writing and editing skills with attention to detail. As part of our team, you will have the opportunity to enhance your research writing skills, gain insights into editing nuances, access articles on industry trends, and receive writing tips through our learning platform. Moreover, you will gain valuable exposure to global research practices. Join us at Pepgra to contribute to impactful publications and regulatory submissions in the field of Orthopaedics.,

As a Medical Writer at our company, you will play a crucial role in creating engaging and compliant scientific content. Your responsibilities will include: - Storyboard Development: - Create structured clinical storyboards for various visual content formats. - Collaborate with design and animation teams to ensure scientific accuracy and narrative flow. - Interpret data and research to develop visually appealing and compliant content. - Scientific Writing: - Draft manuscripts, CME content, and medical articles of various lengths. - Ensure accuracy, referencing, and compliance with scientific and regulatory standards. - Summarize complex data into clear and concise communication for clinicians. - Content Ideation: - Generate topic descriptions and content ideas for client projects. - Identify emerging therapy trends to create innovative scientific content. - Assist in campaign and CME theme conceptualization. Qualifications: - Masters or PhD in Life Sciences, Pharmacy, or Medicine. - Minimum of 15 years of experience in medical writing or scientific communication. - Strong understanding of clinical research, publication standards, and evidence-based medicine. - Excellent research, writing, and communication skills. In addition to the above responsibilities and qualifications, our company values the following core competencies in our Medical Writers: - Scientific accuracy and attention to detail. - Ability to simplify complex medical concepts for a wider audience. - Creative storytelling within clinical contexts. - Collaboration with cross-functional teams to deliver high-quality content.,

Please Note:This opportunity is for overseas placement only!This job is strictly for abroad placements, not for positions within India.Call & WhatsApp: Ms. Pallavi Singh 96-435-99936   Major Roles & Responsibilities   Accounts for coding and abstracting of patient encounters, including diagnostic and procedural information, significant reportable elements, and complications.Researches and analyzes data needs for reimbursement.Analyzes medical records and identifies documentation deficiencies.Serves as a resource and subject matter expert to other coding staff.Reviews and verifies documentation supports diagnoses, procedures and treatment results.Identifies diagnostic and procedural information.Audits clinical documentation and coded data to validate documentation supports services rendered for reimbursement and reporting purposes.Assigns codes for reimbursements, research and compliance with regulatory requirements utilizing guidelines.Follows coding conventions. Serves as coding consultant to care providers.Identifies discrepancies, potential quality of care, and billing issues.Researches, analyzes, recommends, and facilitates a plan of action to correct discrepancies and prevent future coding errors.Identifies reportable elements, complications, and other procedures.Serves as a resource and subject matter expert to other coding staff.Assists lead or supervisor in orienting, training, and mentoring staff.Provides ongoing training to staff as needed.Handles special projects as requested.  

As a PMR Senior Manager at Novartis, you will lead strategic decision-making by collaborating with Product Strategy, Marketing Strategy, cross-functional teams, and Illuminators to support brand growth and optimize launch impact. Your role will involve designing innovative market research approaches, leveraging diverse data sources for evaluating brand performance, and assessing marketing initiatives while ensuring alignment with global and country insights teams. You will drive patient and customer centricity, foster innovation, and share best practices to shape strategy and build a cohesive, forward-looking insights capability. Key Responsibilities: - Define and implement the strategic roadmap for deployment operations. - Ensure deployment processes align with broader marketing and organizational goals. - Serve as the primary point of contact for senior stakeholders and reflect their requirements in deployment strategies. - Present high-level updates and key metrics to executive leadership. - Analyze and report on deployment success trends, identifying areas for improvement. - Establish KPIs for the team and evaluate their contributions against organizational expectations. - Advocate for new technologies and processes to optimize deployment operations. - Drive continuous improvement initiatives by identifying inefficiencies and recommending solutions. - Own the risk mitigation strategy for deployment processes and ensure compliance with security protocols. - Take ultimate responsibility for resolving systemic challenges impacting deployment success. - Act as a bridge between various teams involved in deployment setup and streamline workflows. Qualifications Required: - 10+ years of experience in market research or within specialist agencies. - Extensive experience managing multi-methodology market research projects across multiple markets. - Proven ability to collaborate effectively within a matrix and cross-functional environment. - Expertise in project management, communication, and credibility at a senior level. - Strong business acumen, solution-oriented mindset, and proficiency in budget and P&L management. - Experience in managing remote relationships and delivering on-shore/off-shore capabilities. - Preferred: Familiarity with pharmaceutical disease areas, strong leadership, and communication skills. Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities served. If you need reasonable accommodation for any part of the recruitment process due to a medical condition or disability, please contact diversityandincl.india@novartis.com with your request and contact information.,

As a Medical Science Liaison in Oncology for a Global Pharma MNC, your role will involve building and strengthening the medical affairs presence in oncology by engaging key stakeholders, supporting research, and sharing scientific insights on hard-to-treat cancers. This field-based position will require you to cover India. **Key Responsibilities:** - Engage with Key Opinion Leaders (KOLs), hospitals, and institutions to provide fair and balanced medical information. - Support company-sponsored studies, Investigator-Initiated Trials (IITs), registries, and Real-World Evidence (RWE) projects. - Offer medical expertise and field insights to internal teams. - Collaborate with sales, market access, and other functions to implement regional medical plans. - Ensure compliance with regulations and contribute to patient awareness/ Patient Support Program (PSP) initiatives. **Qualifications Required:** - MBBS/ MD/ PhD with extensive experience in Oncology. - 0-5 years of relevant experience. In addition to the above job responsibilities, ensure that you hold a qualification of MBBS/ MD/ PhD with 12 years of oncology experience. You should possess strong communication skills, stakeholder management abilities, and scientific knowledge. Your capacity to work collaboratively across functions with integrity and business acumen will be crucial. Proficiency in English is mandatory. If you meet the qualifications and experience mentioned above, you are encouraged to reach out to pooja.j@domniclewis.com to expedite the application process.,

As a Clinical Research (CRA) Manager at Medpace, you will be an integral part of the growing clinical operations team based in Navi Mumbai, India. Your main role will involve overseeing the clinical trial management process and ensuring that the team of Clinical Research Associates (CRAs) effectively fulfill their monitoring responsibilities. This position is ideal for individuals seeking a challenging career opportunity to leverage their expertise and enhance their professional growth. **Key Responsibilities:** - Manage a team of CRAs, including recruitment, training, and development to ensure they meet monitoring expectations. - Allocate assignments, track CRA resourcing, and manage turnover and retention in alignment with company objectives. **Qualifications Required:** - Bachelor's degree with 4-6 years of experience in the pharmaceutical industry. - Minimum of 3 years" experience as a CRA and 1-2 years as a CRA Manager. - Advanced knowledge of Good Clinical Practice. - Strong leadership and mentoring skills. - Excellent communication abilities. - Proficiency in Microsoft Office software. - Willingness to travel occasionally for CRA evaluations. Medpace is a prominent full-service clinical contract research organization (CRO) dedicated to accelerating the global development of safe and effective medical therapeutics. With expertise in various therapeutic areas such as oncology, cardiology, and CNS, Medpace aims to positively impact patients" lives worldwide through meaningful work. The company offers a flexible work environment, competitive compensation and benefits, structured career paths for professional growth, employee appreciation events, and health and wellness initiatives. Recognized by Forbes as one of America's Most Successful Midsize Companies and recipient of CRO Leadership Awards, Medpace is committed to fostering a supportive and rewarding work culture. If you are passionate about making a difference in the field of clinical research and contributing to improving healthcare outcomes, we invite you to apply for the Clinical Research (CRA) Manager position at Medpace. Your qualifications will be carefully reviewed, and if there is mutual interest, the team will reach out to you with further details on the next steps. Join Medpace today and be part of the mission to advance medical therapeutics for the benefit of patients worldwide.,

As a Medical Microbiology Faculty at our organization, you will be responsible for the following: - Delivering lectures and conducting practical sessions in the field of Medical Microbiology - Developing and implementing curriculum for students - Guiding and mentoring students in their academic and research projects - Participating in academic and administrative activities of the department To qualify for this role, you should possess one of the following qualifications: - MD in Microbiology or - MSc in Microbiology with a PhD in Medical Microbiology If you are looking for a rewarding opportunity in the field of Medical Microbiology, this position offers competitive salary packages and accommodation based on availability.,

You will be joining Alembic Pharmaceuticals Limited, a renowned pharmaceutical company in India with a rich history dating back to 1907. At Alembic, they specialize in the development, manufacturing, and marketing of pharmaceutical products, substances, and intermediates. Their expertise lies in the Macrolides segment of anti-infective drugs, where they hold a prominent position in the Indian market. With manufacturing facilities in Vadodara and Baddi, Himachal Pradesh, along with cutting-edge research facilities in Vadodara, Alembic is committed to delivering high-quality products to both domestic and global markets, backed by US FDA approved facilities. - Achieving sales targets by promoting and selling Alembic's pharmaceutical offerings to healthcare professionals - Fostering strong relationships with customers - Ensuring customer satisfaction through exceptional service - Visiting healthcare practitioners and providing detailed product information - Addressing customer inquiries and delivering top-notch service to uphold customer loyalty To excel in this role, you should possess a blend of medical sales and customer service skills, coupled with strong communication abilities. A solid foundation in medicine and pharmacy will be beneficial, alongside excellent relationship-building capabilities and a customer-centric approach. The role requires a high level of independence and effective time management skills. - A Bachelor's degree in Pharmacy, Life Sciences, or a related field is essential - Prior experience in medical sales would be advantageous in this position,

As a Freelance Medical & Regulatory Writer at Pepgra scientific editing and publication division, you will play a crucial role in ensuring compliance with EU and US standards and protocols. Your responsibilities will include: - Writing and editing Clinical Evaluation Plans and Clinical Evaluation Reports, as well as other clinical CER deliverables. - Facilitating communication and document exchange between various stakeholders, both internal (Regulatory Affairs, R&D, Clinical R&D, Sales and Marketing, etc.) and external (CROs, Medical Writers, Reviewers). - Providing strategic guidance on regulatory requirements to new product development and sustaining teams. - Writing and editing clinical study protocols, reports, regulatory briefing documents, and safety update reports. - Managing document reviews and ensuring quality control for adherence to regulatory guidelines. - Supporting technical/clinical/regulatory writing for global regulatory submissions. - Writing and maintaining Standard Operating Procedures and Style Manuals. - Preparing manuscripts, review articles, abstracts, posters, and presentations according to ICMJE standards. - Quality auditing all documents before publishing. To excel in this role, you will need: - A PhD/Masters/Bachelors degree or expertise in healthcare, medicine, surgery, or Cancer Research. - Excellent English editing skills with a keen eye for detail. - AMWA/EMWA certification would be a valuable addition. Subject areas that you may be working on include, but are not limited to: Medicine: - Anesthesiology and pain medicine - Dentistry - Internal medicine - Immunology - Genetics - Ophthalmology - Radiology - Respiratory care - Veterinary sciences Allied Healthcare: - Diabetes research - Emergency and critical care - Geriatric medicine - Infectious diseases - Nursing and hospital medicine - Public health - Clinical Allergies Cancer Research: - Chemo radiotherapy - Molecular cancer research - Radiotherapy planning Organ systems, physical medicine, and rehabilitation: - Cardiology - Dermatology - Gastroenterology - Obstetrics and Gynaecology - Orthopedics - Paediatrics - Plastic and reconstructive surgery - Sports medicine - Urology - Cardiology Surgery This position offers you the flexibility to manage your schedule, potential high earnings based on availability, and continuous learning opportunities. Additionally, you will receive regular feedback on your freelance editing assignments.,

Role Overview: As an Associate Director, Safety Writing at GSK, you will be responsible for leading the safety writing team and ensuring accurate, clear, and compliant preparation of Aggregate Reports and Risk Management Plans (RMP). Your role will involve managing a team of in-house medical writers, providing oversight and input into all aspects of aggregate reports and RMP preparation, and driving key organizational process improvement initiatives. Your contribution will play a crucial role in impacting the health of millions of people worldwide. Key Responsibilities: - Manage a team of 8-10 in-house medical writers to develop aggregate reports and RMPs in scope to support delivery of the portfolio. Identify needs for development and capability expansion of team members. - Ensure medical writers are trained in relevant procedures, policies, and standards for safety writing activities. Lead the development of training materials and provide mentoring and coaching to individuals or teams. - Evaluate resources required for safety writing activities to align with organizational objectives. Provide project updates to leadership and propose solutions for shifting timelines and staffing requirements. - Interface with cross-functional safety teams and third parties to ensure appropriate input and alignment for the resourcing and generation of safety reports. - Drive and implement key organizational process improvement initiatives, generate ideas for improvement, and promote an empowering environment for idea generation. - Provide leadership, strategic planning, delegation of responsibilities, and tasks. Monitor project progress and assess overall performance. - Measure and monitor efficiency and quality of the team's output, collect and evaluate metrics to identify the need for process improvement. Qualification Required: - Minimum qualification required is a master's degree in Life Sciences/Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.). A degree in Medicine/Dentistry/Physiotherapy/Experimental Medicine is advantageous. - 6-8 years of experience in safety writing, including leading the development of safety reports in a post-market setting within the pharmaceutical/Contract Research Organization industry. Company Details: GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. With a focus on impacting the health of 2.5 billion people by the end of the decade, GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing. The company's innovative approach to discovering and delivering vaccines and medicines aims to transform lives and accelerate significant assets that meet patients" needs with the highest probability of success.,

Your day-to-day responsibilities: - Identify and establish strategic partnerships with hospitals and healthcare institutions to promote Emoha's home care services, subscription plans, and value-added offerings. - Develop and activate channels to engage with doctors, specialists, and medical professionals to generate referrals and leads for home care cases. - Proactively identify potential leads and opportunities within the healthcare ecosystem, including hospitals, clinics, nursing homes, and other healthcare providers. - Leverage existing relationships and networks in the healthcare industry to expand Emoha's presence and foster collaboration with key stakeholders. - Implement targeted sales and marketing strategies to promote Emoha's services to hospitals, doctors, and healthcare professionals. - Build and maintain strong relationships with key decision-makers, influencers, and opinion leaders in the healthcare sector. - Conduct market research and analysis to identify market trends, competitor activities, and opportunities for growth. Benefits: - Cell phone reimbursement - Health insurance - Paid sick time - Provident Fund Work Location: Remote,

As a Business Process Management company, you will be responsible for various tasks including populating databases with information from multiple sources, extracting data for analyst teams, creating PowerPoint and Excel templates, interpreting data for presentations, and conducting statistical analysis on market research data. Additionally, you will be involved in data validation, quality checks, editing reports, and identifying discrepancies in text and data tables. To qualify for this role, you will need an undergraduate degree with a strong academic record, preferably in Business or Commerce. An advanced degree or relevant experience in the biopharma, healthcare, or market research sector would be advantageous. Attention to detail, analytical skills, proficiency in SPSS software, and excellent English communication skills are essential. Proficiency in software like E-tabs, SQL, and Tableau, as well as a collaborative and flexible approach to work, are desired qualities. You should possess strong critical thinking skills, time management abilities, self-motivation, and the capacity to work under pressure and meet deadlines. The role also requires initiative, adaptability to process improvements, and proficiency in Microsoft Word, Excel, and PowerPoint. Knowledge of pharmaceutical or medical device industries and experience in data visualization are assets but not mandatory. In this fast-paced environment, you will be expected to handle multiple requests efficiently and demonstrate excellent written and verbal communication skills. The position may involve rotational shifts, and a minimum of 2 years of SLA is required. Moreover, you should have excellent communication skills and be capable of working effectively in a team setting. Please note that you should be prepared to question assumptions, theories, and facts, provide new ideas, and adapt to process improvements. Overall, your role will be crucial in supporting the company's client deliverables and ensuring data accuracy and professional presentation.,

As a Marketing Executive (Medical) at Otsuka Nutraceutical India Pvt. Ltd. in Ahmedabad, your role will involve promoting the company's pharmaceutical and nutraceutical products through field marketing activities. You will be responsible for building and nurturing strong relationships with healthcare professionals and pharmacists. Additionally, you will play a crucial role in providing feedback on market trends, competitor activities, and customer needs. Timely reporting and documentation as per company norms will be a key part of your responsibilities. You will also be involved in performing sampling activities, BTL activations, and participating in CMEs, Medical Conferences, and other medical marketing events. Qualifications Required: - A Bachelor's degree in pharmacy or science is preferred. - Additional qualifications in Marketing will be advantageous. Key Responsibilities: - Conduct field marketing activities to promote pharmaceutical and nutraceutical products. - Build and maintain relationships with healthcare professionals and pharmacists. - Provide feedback on market trends, competitor activities, and customer needs. - Ensure timely reporting and documentation. - Perform sampling activities and BTL activations. - Participate in CMEs, Medical Conferences, and other medical marketing events. Experience: - 2 to 4 years of relevant experience in the pharmaceutical, nutraceutical, or B2C industries. - Prior experience as a Medical Representative (MR) is preferred. - Field marketing experience is essential. Other Requirements: - Good communication and interpersonal skills. - Ability to work independently and travel within the territory. - Familiarity with the Ahmedabad City landscape is a plus. If you are interested in this opportunity, please share your CV at shivani.patil@otsukanutraceutical.in or contact +91 86554 81558.,