4 internal Medicine Jobs nearby Bangalore

Job description Roles and Responsibilities Provide high-quality patient care to patients with various medical conditions, including acute and chronic illnesses. Conduct thorough physical examinations, take medical histories, and order diagnostic tests as needed. Develop treatment plans for patients based on their individual needs and medical history. Collaborate with other healthcare professionals to ensure comprehensive care for patients. Stay up-to-date with latest medical research, guidelines, and best practices in internal medicine. Desired Candidate Profile 0-5 years of experience in general medicine or related field. Medical-MS/MD degree from a recognized institution. Strong knowledge of general medicine principles, diagnosis, and treatment options.

Medicine Specialistdiagnoses and treats a wide range of diseases and conditions, primarily in adults. Key responsibilities include conducting physical exams, interpreting diagnostic tests, developing and implementing treatment plans, prescribing medication, and collaborating with other healthcare professionals. They must also maintain accurate patient records and stay current with medical advancements through continuous learning. Core responsibilities    Patient care: Conduct thorough physical exams and patient interviews to diagnose and manage a wide range of medical conditions.    Treatment planning: Develop and implement personalized treatment plans, which may include prescribing medications, therapies, or surgical referrals.    Diagnostics: Order and interpret laboratory tests, imaging studies, and other diagnostic procedures to inform diagnoses.    Collaboration: Work closely with other healthcare professionals, such as nurses, specialists, and other physicians, to provide comprehensive and holistic care.    Communication: Clearly explain diagnoses, treatment options, and potential side effects to patients and their families.    Documentation: Maintain accurate and confidential patient records, including medical history, treatment plans, and progress notes.    Professional development: Stay up-to-date with the latest medical research, advancements, and best practices in internal medicine.    Preventative care: Advise patients on healthy habits and preventative measures to promote overall healthRequired qualifications    Doctor of Medicine or degree from an accredited institution.    Valid medical license to practice.    Board certification in a relevant specialty, such as Internal Medicine.    Residency training in their specialty.    Strong clinical, diagnostic, and analytical skills.    Excellent communication and interpersonal skills.

As a Manager Regulatory Affairs, Labeling at Teva Pharmaceuticals, you will be responsible for setting strategic goals, managing and leading teams, driving operational efficiency, and making high-level decisions that impact the team's success. You will supervise, critically review, and approve established US Gx labeling documents filed under an ANDA/505(b)2s while ensuring compliance with federal regulations, internal processes, and meeting timelines aligned with company goals. Additionally, you will oversee team databases and trackers to ensure projects remain on track. Key Responsibilities: - Establish and implement labeling strategies for all US generic product ANDAs/505(b)2s, both pre and post-approval - Ensure compliance with all FDA reporting obligations according to business objectives and regulations - Provide guidance on best practices in the labeling arena - Lead daily workload activities and assign labeling projects - Develop, review, and compile labeling documents in alignment with RLD, FDA safety changes, company initiatives, and submission requirements - Maintain labeling trackers and ensure project timelines are met - Expertise in Structured Product Labeling (SPL) to align with FDA regulations and guidances - Collaborate with Regulatory Operations to meet submission deadlines following eCTD requirements - Coordinate with external departments to align with product strategy for pre and post-approval portfolio - Attend relevant meetings and create/revise SOPs/WIs as needed - Stay updated on US regulations, guidelines, and SOPs/WIs related to US Gx labeling - Experience in developing labeling content requiring carve outs due to protected language associated with patent/exclusivities is preferred Qualifications Required: - MPharm/BPharm with a Scientific or Regulatory background or equivalent - Minimum 8 years of US labeling experience and at least 3 years of supervisory experience preferred - Minimum 8 years of Pharmaceutical industry experience, specifically in Regulatory Affairs & US ANDA/505(b)(2) labeling As a part of Teva Pharmaceuticals, you will contribute to the mission of making good health more affordable and accessible to help millions around the world enjoy healthier lives. With a diverse workforce spread across nearly 60 countries, you will have the opportunity to work with the world's leading manufacturer of generic medicines and play a vital role in improving global healthcare. Apply now to be a part of our mission and make a difference!,

As a Clinical Coder at Bengaluru Luxor North Tower, your role will involve the following key responsibilities: - Understanding the scope of requests and generating and maintaining sets of medical and pharmacy codes for use in studies using healthcare data - Driving stakeholder engagement by identifying coding needs for real-world database studies - Maintaining a coding library platform to store code sets and support re-use of standardized code sets - Identifying opportunities for automation in code list generation process - Conducting effective literature reviews to create/update code lists accurately - Documenting and archiving code lists in the coding library platform - Updating the Repository data internal platform dictionary with latest codes when external tools are unavailable - Learning and delivering code lists for new coding systems used in different datasets - Providing guidance and support to project teams/vendors on Clinical coding process - Defining and driving metrics and reports creation for Senior Management - Identifying process improvements and implementing innovative solutions for efficiency and quality enhancement Qualifications required for this role include: - MSc/PhD in Life Science, B-Pharm/ M-Pharm/ medicines - Minimum 10 years of experience in clinical coding - Proficiency in using coding systems such as ICD-10-CM, HCPCS, CPT, NDC, SNOMED, LOINC, etc. - Familiarity with tools/systems to retrieve codes - Understanding of regulatory guidelines and compliance requirements related to clinical coding - Experience with AI/ML tools for code list generation process - Expertise in R with proficiency in other programming languages such as SQL and visualization tools - Excellent problem-solving skills and ability to think strategically At Bengaluru Luxor North Tower, you will be part of a global biopharma company with a purpose to positively impact the health of 2.5 billion people by the end of the decade. The company is committed to creating an environment where people can thrive and focus on making a difference in patients" lives. If you are looking for an opportunity to be part of a successful and growing company where innovation and impacting health at scale are priorities, then this role might be the perfect fit for you. If you require any adjustments during the recruitment process, feel free to reach out to our Recruitment Team at IN.recruitment-adjustments@gsk.com. Please note that GSK does not accept referrals from employment businesses/agencies without prior written authorization. If you come across any unsolicited emails or job advertisements not ending in gsk.com, please inform us at askus@gsk.com to verify the authenticity of the job.,

As the Manager, Regional Traffic & Customs Operations at Apotex Inc., your main responsibility is to oversee all Transportation and Logistics functions for assigned origin operations, including Freight and Transportation, Freight Forwarding, and Customs Clearance. You will collaborate with various internal and external stakeholders to ensure the efficient and cost-effective movement of goods from India, China, and Europe, aligning with departmental and corporate strategic plans. Your key responsibilities will include: - Liaising with Global External Operations, ARPL, Global Traffic & Customs, CMOs, and Freight Forwarder for planning and execution of full loads, reporting on cost savings and missed opportunities - Managing Regional Freight Forwarder performance and relationships - Planning, executing, managing, and monitoring temperature-sensitive shipments for product quality and regulatory compliance - Participating in the development of long-term planning, recommending process improvements, and proposing cost-effective transportation methods - Providing regional transportation updates, KPIs, and actionable insights for strategic decision-making - Evaluating various modes of transportation, making recommendations to Management for approval - Collaborating with internal departments/customers for document preparation and shipment scheduling - Recommending actions for non-compliance with international customs and regulatory agencies - Developing and maintaining relationships with external stakeholders to support cost-effective movement of goods - Participating in cross-functional project teams, systems, policies, and procedures implementation - Providing detailed timelines for regional traffic investigations and collaborating with Transportation provider - Ensuring completeness of shipments with required documentation and overseeing the shipment process - Responding to complex queries regarding regional Traffic and Customs issues - Working in accordance with established regulatory, compliance, and safety requirements - Demonstrating organizational values: Collaboration, Courage, Perseverance, and Passion - Adhering to all compliance programs including Global Business Ethics, Quality policies, Safety and Environment policies, and HR Policies For this role, you should have: Education: - University degree in Business, Science, Supply Chain/Operations, or related field - MBA and/or PMP certification (considered an asset) - Recognized designation (FITT, ASCM, CITT, P.Log) and/or Lean Six Sigma certification (considered an asset) Knowledge, Skills, and Abilities: - Excellent knowledge of INCO terms, AMPs, TDG, FDA, and DEA terms and requirements - Strong interpersonal and communication skills - Flexibility to work during different time zones - Ability to deal with ambiguity and manage through difficult situations - Strong working knowledge of enterprise systems and supply chain practices - Experience leading teams and driving improvements - Computer literacy with MS Office suite of tools Experience: - 10-15 years in Freight Forwarding, Logistics, Customs, or Supply Chain environment - Pharmaceutical industry experience preferred Join Apotex Inc. to contribute to improving access to affordable, innovative medicines and health products globally.,

You will be responsible for providing scientific and technical expertise of the highest standards for local medical information, including interactions with Key External Experts (KEEs) and Key Opinion Leaders (KOLs). Additionally, you will provide medical and scientific input and information for business strategy for the region. Key Responsibilities: - Develop and sustain credible networking with appropriate Health Care Practitioners (HCPs). - Plan, facilitate, and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and other product-specific campaigns. - Deliver scientific presentations with consistent messages for key products at various meetings. - Support scientific presentations at medical education meetings. - Understand and support Scientific Engagement (SE) activities as per Medical Plans. - Become an expert in oncology for GSK brands and associated activities. - Stay updated on scientific knowledge in oncology, GSK molecules, and their PI for effective on-label communications. - Support in the feasibility assessment of potential research sites, develop concept notes, proposals, budgets, and monitoring tools for field studies. - Provide medical inputs into the development and execution of brand strategy. - Support Named Safety contact in strengthening oncology Pharmacovigilance. - Ensure continuous self-learning in Pharmacovigilance. Qualifications Required: - Minimum Level of Education: MBBS with post-graduate qualification. - Preferred Level of Education: Post-graduate qualification in Pharmacology/Public Health. - Preferred Education Level Reason: To interact effectively with specialized HCPs. Job-Related Experience: - Excellent written and oral communication skills in English and the local language. - Experience presenting scientific topics in various settings. - Solid understanding of ICH-GCP principles and internal SOPs. - Ability to comprehend scientific methods and experimental design. - 1-2 years in the pharmaceutical industry, preferably in oncology therapy with a preference for Hemato-oncology. Other Job-Related Skills/Background: - Presentation skills at scientific meetings. - Effective communication skills, both verbal and written. - Technical writing skills. - Ability to stay updated with new developments. - Capacity to provide and receive constructive feedback. - Build and maintain relationships with colleagues. - Share knowledge with team members. - Collaborate effectively within a team to achieve common goals. - Contribute creative ideas for continuous improvement. - Develop strong relationships with key opinion leaders. --- **About the Company:** GSK is a global biopharma company focused on uniting science, technology, and talent to get ahead of disease together. Their purpose is to positively impact the health of 2.5 billion people by the end of the decade. GSK aims to prevent and treat diseases with innovation in specialty medicines and vaccines across therapeutic areas such as respiratory, immunology, inflammation, oncology, HIV, and infectious diseases. The company values creating an environment where employees can thrive and focus on delivering for patients, shareholders, and the community. **Inclusion at GSK:** As an inclusive employer, GSK encourages candidates to reach out if they require any adjustments during the recruitment process. Candidates can contact the Recruitment Team at IN.recruitment-adjustments@gsk.com to discuss their needs. --- **Note:** GSK does not accept referrals from employment businesses/agencies without prior written authorization. If you receive unsolicited emails from email addresses not ending in gsk.com or job advertisements with suspicious instructions, please inform GSK at askus@gsk.com to verify the job's authenticity.,

As a Regional Medical Advisor (RMA) for General & Specialty Medicine in the South Region, you will play a crucial role as a key representative for the company. Your primary objective will be to engage with essential stakeholders in the field and provide scientific expertise across identified regions, products, and therapy areas to valued customers. **Responsibilities and Primary Activities:** - **Scientific Expertise:** Develop and maintain a comprehensive understanding of the company's products, particularly in the cardiovascular therapeutic area. Stay updated on the latest medical advancements, clinical guidelines, and treatment protocols. - **Stakeholder Engagement:** Build and maintain relationships with Scientific Leaders (SLs), Key Decision Makers (KDMs), healthcare professionals, and academic institutions. Engage in scientific discussions, present clinical data, and provide educational support to Key Opinion Leaders (KOLs) regarding the company's products and therapeutic areas. - **Support to Medical Strategy:** Collaborate with the line manager to provide strategic inputs and expertise to product management. - **Medical Education:** Deliver scientific and medical education to internal stakeholders, including sales and marketing teams. Collaborate with the Medical Affairs team to develop and present training materials. - **Scientific Exchange:** Facilitate knowledge transfer between the company and external stakeholders by participating in medical conferences, advisory boards, and scientific meetings to gather insights and share data. - **Clinical Data Communication:** Interpret and communicate clinical trial data, real-world evidence, and other scientific information to healthcare professionals and regulators, ensuring compliance with regulations and company policies. - **Clinical Research Support:** Provide medical support for local studies, including identifying study sites for Investigator Initiated Trials. - **Cross-Functional Collaboration:** Work closely with Clinical Development, Regulatory Affairs, Marketing, and Market Access teams to provide scientific input, support clinical trial design, and align on medical communication plans. - **Medical Initiatives:** Support and lead medical projects aligned with the therapy area, involving strong stakeholder interaction. - **Medical Information:** Address medical inquiries and provide timely, accurate responses to healthcare professionals and other stakeholders, ensuring that medical information materials are current and compliant. - **Sales Force Training:** Train sales colleagues on assigned therapy areas and assist in pre-launch and launch training for new products. - **Compliance:** Adhere to legal, regulatory, and compliance guidelines, ensuring all activities are conducted ethically and in accordance with applicable laws. **What You Must Have:** - **Educational Background:** A strong academic foundation in life sciences, such as a medical degree (MD) or doctorate (Ph.D.). - **Industry Experience:** At least 1 year of experience in the pharmaceutical cardiovascular therapy area, including roles in clinical research or medical affairs. - **Therapeutic Area Expertise:** Demonstrated knowledge and expertise in the relevant cardiovascular therapeutic area. - **Scientific and Clinical Knowledge:** Strong understanding of medical and scientific principles, clinical trial design, data analysis, and interpretation. - **Communication and Relationship-Building Skills:** Excellent interpersonal, communication, and presentation skills. - **Analytical and Problem-Solving Skills:** Ability to analyze complex scientific data and provide recommendations. - **Adaptability and Flexibility:** Capability to work in dynamic environments and travel frequently. - **Regulatory and Compliance Knowledge:** Familiarity with legal, regulatory, and compliance guidelines. In summary, as an RMA in Medical Affairs, you will act as a scientific expert and liaison between the company and external stakeholders, contributing to building scientific credibility, fostering relationships, and supporting strategic objectives in the healthcare industry.,

Role Overview: As a Local Case Intake Advisor (Chinese language) at Global Business Services, you will be responsible for managing the intake, processing, and reporting of individual case safety reports (ICSRs) at the local level. Your role will involve supporting specific local Marketing Companies to ensure compliance with AstraZeneca (AZ) and relevant national regulatory requirements, acting as the primary liaison between Marketing Companies and GBS-PS. Your fluency in English will be crucial as you work under the guidance of Case Intake Team Managers to deliver routine activities independently, resolve moderate scope problems, and maintain compliance with standards. Key Responsibilities: - Support the provision of pharmacovigilance activities including local processes, procedures, and systems for collection, reporting, and tracking of Adverse Events (AEs). - Review, assess, and process safety data from various sources, distributing reports to internal and external third parties. - Identify Product Quality Complaint (PQC) and Product Security complaints, collecting necessary information for AE complaint reporting. - Provide prompt support for regulatory authority queries related to the Patient Safety function. - Implement Corrective and Preventative Actions in the event of local non-compliance. - Ensure reconciliations for the accuracy of pharmacovigilance data transferred and received. - Periodically screen regulatory authority databases for adverse events. - Perform literature search and related activities for MC product portfolio if required. - Undertake manual follow-up where required, disseminating clear and accurate information based on approved call scripts. - Maintain filing and archiving practices of patient safety documents. - Actively contribute to maintaining Good Pharmacovigilance Practice and being audit and inspection ready. - Support external service providers to meet company and local regulatory PV requirements. - Assist the local PS team in audits or regulatory authority inspections. - Complete all required patient safety trainings and obtain access to relevant systems. - Maintain current knowledge of relevant country regulatory authority regulations, global and local procedural documents, marketed status of products, and conditions relating to product safety. Qualifications Required: - Degree Qualified in Pharmacy/Medical/Science - Language skill in Chinese - Pharmacovigilance knowledge excellence - Good Pharmacovigilance Practice - Knowledge of health authority regulations - Cross-functional collaborative approach - Effective and lateral thinking - Problem-solving skills - Vendor management experience - Excellent attention to detail - Excellent written and verbal communication skills Additional Company Details (if present in JD): At AstraZeneca, the work directly impacts patients by transforming the ability to develop life-changing medicines. The company empowers the business to perform at its peak by combining cutting-edge science with leading digital technology platforms and data. Joining AstraZeneca provides the opportunity to innovate, take ownership, and explore new solutions in a dynamic environment that encourages lifelong learning. The company values in-person collaboration to unleash bold thinking and inspire life-changing medicines, balancing office expectations with individual flexibility. If you are ready to make a difference and contribute to the development of life-changing medicines, apply now to join the AstraZeneca team!,

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 an experienced Life Sciences Subject Matter Expert (SME) with expertise across Commercial Analytics and R&D functions, your role will involve partnering with clients to shape solution strategies, evangelize data-driven offerings, and drive innovation across the drug development and commercialization lifecycle. Acting as a trusted advisor to senior stakeholders, you will also enable internal teams to design and deliver impactful solutions. **Key Responsibilities:** - **Commercial Analytics Strategy & Enablement** - Evangelize advanced analytics solutions in areas such as sales & marketing effectiveness, patient journey analytics, market access, pricing & reimbursement, and digital engagement. - Guide biopharma and medtech clients on leveraging real-world data (RWD), claims, EMR, and patient registries to optimize brand performance and market share. - Support forecasting, targeting, segmentation, and omnichannel analytics to maximize commercial impact. - **R&D & Clinical Development Insights** - Advise on applying AI/ML and advanced analytics in drug discovery, clinical trial design, site selection, patient recruitment, and safety monitoring. - Promote solutions around clinical operations optimization, trial feasibility, and biomarker-driven development. - Drive integration of RWD, clinical, genomic, and digital biomarker data to accelerate R&D decision-making. - **Data-Driven Innovation** - Partner with data engineers and analytics teams to design dashboards, predictive models, and GenAI/Agentic AI solutions supporting both commercial and R&D use cases. - Shape innovative offerings for functions like medical affairs insights, pharmacovigilance automation, and evidence generation. - Guide strategies for harmonizing structured and unstructured data (e.g., publications, trial protocols, regulatory submissions) for actionable insights. - **Stakeholder Engagement & Business Development** - Lead requirement workshops, solution strategy discussions, and roadmap design with client stakeholders. - Collaborate with sales and business development teams by providing SME support in pursuits, RFP responses, and client presentations. - Act as a bridge between client needs and technical delivery teams to ensure alignment on business value. - **Regulatory, Compliance & Thought Leadership** - Stay current with global regulatory requirements (FDA, EMA, ICH, GxP, GDPR, etc.) and industry trends affecting both commercial and R&D domains. - Contribute to whitepapers, industry forums, and client education sessions to position the organization as a leader in life sciences analytics. - Monitor emerging trends in digital health, decentralized trials, and personalized medicine to inform solution innovation. **Qualifications Required:** - 8-10 years of experience in Life Sciences industry consulting, commercial analytics, or R&D strategy. - Strong understanding of pharma/biotech value chain, spanning R&D, clinical, regulatory, market access, and commercial operations. - Hands-on experience with healthcare data sources: claims, EHR, registries, RWD, RWE, genomics, clinical trial data.,

Role Overview: As an Administrative Support for the Clinical Systems at our company, you will be responsible for providing guidance and assistance in various administrative tasks related to the Clinical Systems. Your essential functions will include but are not limited to: Key Responsibilities: - Handling internal User Access management requests for Clinical Systems and other business systems. - Entering data into the Global Directory within Precisions Clinical System across all Sites, Institutions, and updating as necessary. - Creating Studies, Countries, and Sites within the Clinical System as per requests. - Addressing help desk tickets to answer questions, troubleshoot problems, and identify system performance issues or deficiencies. - Supporting Clinical System modifications and updates to picklists, field requirements. - Assisting Clinical teams in reviewing Clinical System access and removing access as needed. - Supporting leads or managers in any ad-hoc tasks assigned. Qualifications Required: - Degree, or equivalent combination of education and experience in information systems or technology. Other Details of the Company: Please note that any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice. If you require a reasonable accommodation to complete any part of the application process due to a disability or limitations in accessing the online application process, please contact Precision Medicine Group at QuestionForHR@precisionmedicinegrp.com. Please be cautious of fraudulent offers from individuals or organizations posing as potential employers. Our organization follows a formal interview process and does not extend job offers without prior communication with our recruiting team and hiring managers.,

Role Overview: As a Supervisor of the Sample Management Support team in Bangalore, India, you will play a crucial role in supporting the client facing Sample Management team for various sample management activities. Your responsibilities will involve leading a team of specialists, collaborating with key stakeholders, and ensuring the smooth execution of all data activities related to sample management. Your close coordination with internal stakeholders will be vital in delivering study setup, sample handling, shipment coordination, data reconciliation, and study close-out activities. Key Responsibilities: - Assist in setting up new studies by understanding study design and sample management requirements. - Support site training by creating targeted materials for documentation compliance, sample handling, and shipment. - Aid in data entry tasks, including data discrepancies, EDC reconciliation, and e-portal management. - Coordinate courier and logistics needs, including setup, scheduling, tracking, and coordination between sites, labs, and clients. - Reconcile data and track sample collections and kits across various sites. - Handle data reporting needs for study queries and generate sample management reports. - Ensure client deliverables are appropriately billed and documented. - Document sample-related issues, corrections, and compliance with QMS standards. - Assist in study close-out activities, including sample inventory transfers/destruction and document close-out. Qualifications: Minimum Requirements: - Minimum of 6 years of relevant experience. - At least 3 years of leadership or supervisory experience. - Proficiency in managing diverse clinical research tasks. - Comprehensive understanding of drug, device, and/or biologic development processes. - Experience with clinical database management systems. - Strong expertise in data quality standards and practices. - Proficiency in Microsoft Office Suite. Preferred Qualifications: - Background in clinical, scientific, or healthcare disciplines. - Familiarity with data privacy regulations (e.g., GDPR, HIPAA). - Experience with Power BI, Power Query, and/or Power Automate. - Knowledge of Laboratory Information Management Systems (LIMS) and Biospecimen Inventory Systems. - Experience using Smartsheet for project tracking and collaboration.,

You will be responsible for the assessment, diagnosis, treatment, and management of patients with a wide range of acute and chronic medical conditions. You will work under the supervision of Consultant Physicians to provide high-quality patient care. Key Responsibilities: - Assessing patients" medical conditions - Making accurate diagnoses - Developing and implementing treatment plans - Managing patients" ongoing care - Collaborating with other healthcare professionals - Keeping detailed and accurate medical records Qualifications Required: - MD or DNB in Internal Medicine Experience: - 0-3 years of experience, freshers can also apply Work Type: - Full-time Benefits: - Paid sick time - Paid time off Work Location: - In person,

Role Overview: You will be responsible for engaging with key opinion leaders (KOLs) and healthcare professionals (HCPs) in the fields of medical genetics, genomics, reproductive medicine, oncology, and other relevant specialties. Your role will involve presenting scientific and clinical data accurately, serving as the primary scientific contact for genetics-based products and services, and participating in scientific advisory boards, conferences, and symposia. Additionally, you will support the development and delivery of scientific training programs for internal teams, conduct educational sessions and academic presentations for external stakeholders, and assist in creating and reviewing medical/clinical content. Key Responsibilities: - Build and maintain strong relationships with KOLs and HCPs - Present scientific and clinical data accurately - Serve as the primary scientific contact for genetics-based products and services - Participate in scientific advisory boards, conferences, and symposia - Support the development and delivery of scientific training programs - Conduct educational sessions and academic presentations - Assist in creating and reviewing medical/clinical content - Provide scientific support for clinical trials and post-marketing studies - Collect and report medical insights from the field - Support clinicians with test interpretation and report explanation - Ensure compliance with regulatory, ethical, and legal guidelines - Maintain up-to-date knowledge of relevant literature, genetic technologies, and clinical guidelines Qualifications: - PhD, MD, BDS, MDS, with specialization in Medical Genetics, Molecular Biology, Genomics, or related fields Company Details: HaystackAnalytics is a HealthTech company that specializes in creating clinical genomics products to enable accurate and personalized diagnostics. Supported by India's most respected science agencies, the company has launched innovative genomics-based diagnostic solutions for infectious diseases. Their products have been recognized for their impact and were even launched by the Prime Minister of India at a prestigious event. (Note: Skills section has been omitted as it does not directly contribute to the job description),

As a Safety Specialist II at our company, your role will involve the following responsibilities: - Authoring and reviewing various Aggregate Safety Reports such as DSURs, PBRERs, PSURs, PADERs, and Canadian Aggregate Reports as required by the project. - Reviewing aggregate safety data, generating line listings (LL) and summary tabulations (ST), and incorporating them into the appropriate templates. - Analyzing safety and regulatory data provided by clients to prepare comprehensive Aggregate Reports. - Conducting literature screening to include significant safety articles in the respective sections of aggregate reports. - Compiling benefit-risk evaluation sections provided by medical reviewers. - Ensuring compliance with internal and external timelines and addressing comments from reviewers. - Participating in audits and inspections by clients and health authorities. In addition, you will be responsible for: - Screening, data mining, and frequency tabulation for potential signals, including signal estimation using appropriate tools. - Drafting signal detection, validation, assessment, and benefit-risk analysis. - Developing Risk Management Plans in alignment with specific SOPs. - Tracking identified signals and monitoring their status. - Supporting the Individual Case Safety Report and Literature review teams as needed. - Assisting in report scheduling and demonstrating a good understanding of medical and Pharmacovigilance terminologies. - Having knowledge of GCP, GVP, ICH, USFDA guidelines, and other relevant regulations. - Possessing basic competence in medical and therapeutic terminology. - Demonstrating a strong understanding of patient safety regulatory obligations. - Being familiar with regulatory and pharmacovigilance guidelines. - Having proficiency in written and spoken English, with additional languages being advantageous. - Having good command over MS Office tools. - Exhibiting soft skills such as motivation, communication, organization, reliability, and teamwork. If you join us in Bangalore, India, you should hold a graduate or postgraduate degree in life sciences, pharmacy, medicine, dentistry, allied health sciences, or related fields. This is a full-time role in the Analyst category under Regulatory Affairs.,

As a Junior Consultant at Sahyadri Narayana Multispeciality Hospital in Shimoga, Karnataka, your role will involve managing inpatient, outpatient, and critical care responsibilities in the field of Cardiology. You will work closely with senior cardiologists, multidisciplinary teams, patients, and families to ensure continuity of care while adhering to hospital protocols and professional standards. Key Responsibilities: - Conduct and document detailed patient history and physical examinations - Formulate differential diagnoses - Prepare daily progress notes and discharge summaries - Develop, implement, and modify individualized care plans - Order and interpret relevant laboratory, radiological, and hemodynamic investigations - Prescribe medications and order blood transfusions as required - Perform and interpret echocardiography, ECGs, and other non-invasive cardiac assessments - Monitor and interpret hemodynamic parameters in critically ill patients - Perform CPR, endotracheal intubation, nasogastric intubation, and insert invasive lines under supervision - Assist cardiologists in invasive procedures - Independently perform basic Cath Lab procedures under supervision - Obtain informed consent for procedures - Provide patient and family education regarding diagnosis, treatment options, and prognosis - Conduct OPDs in the absence of senior cardiologists - Manage inpatient cases and coordinate with multidisciplinary teams - Ensure continuity of care - Work under the supervision of senior consultants - Maintain accurate records - Comply with hospital policies - Contribute to departmental academic and clinical discussions Qualifications Required: - MBBS/MD/DNB/DM in Cardiology - 0 - 3 years of relevant clinical experience in Cardiology or Internal Medicine In addition to the specific responsibilities mentioned above, your role will require proven ability to conduct patient history, physical examinations, diagnoses, progress notes, and discharge summaries. You should also have proficiency in performing and interpreting ECGs, echocardiography, laboratory, and radiology results, with experience in managing critically ill patients. Strong communication skills and the ability to interact empathetically with patients, families, and multidisciplinary teams are essential for this position. Demonstrating reliability, attention to detail, and effective collaboration in high-pressure clinical environments will be key to success in this role.,

Job Description: You will be responsible for teaching and conducting research in the field of Internal Medicine. Your key responsibilities will include: - Providing lectures, seminars, and practical demonstrations to medical students - Supervising the clinical work of medical students and residents - Participating in academic and administrative activities of the department To qualify for this position, you must have: - MBBS degree - MD/DNB in General Medicine - Eligibility as per NMC norms Please note that the salary offered for this position is the best in the industry. This is a full-time, permanent role located in Bangalore/Tamil Nadu where you will be required to work in person.,

As an Internal Medicine MD DNB Consultant at Shivamoga, Karnataka, you play a crucial role in delivering comprehensive medical care and consultation to a diverse range of patients. Your expertise and contributions significantly impact the overall patient care and treatment strategy. Key Responsibilities: - Conduct detailed patient assessments and medical histories - Order and interpret diagnostic tests and procedures - Formulate and execute effective treatment plans - Provide medical consultation and guidance to patients and their families - Oversee chronic medical conditions - Collaborate with healthcare team members for holistic patient care - Engage in medical research and clinical trials - Participate in quality improvement initiatives at departmental and hospital levels Qualifications Required: - MD or DNB in Internal Medicine - Valid state medical license in Karnataka - Demonstrated experience as an Internal Medicine Consultant - Thorough understanding of internal medicine principles and practices - Proficiency in clinical and diagnostic skills - Excellent communication and interpersonal capabilities - Ability to thrive in a multidisciplinary team environment - Commitment to continuous professional development - Dedication to delivering high-quality patient care - Adherence to medical ethics and confidentiality standards In addition to the core responsibilities, you are encouraged to engage in medical research, clinical trials, and quality improvement initiatives to enhance patient care. Your expertise in ethics, healthcare, professional development, medical consultation, confidentiality, clinical and diagnostic skills, internal medicine, and communication will be instrumental in your success in this role.,

At nFerence Labs, you will be part of the team building the world's first large-scale computational platform for reverse engineering biology, known as the "Google of Biomedicine." **Key Responsibilities:** - Work closely with the software and data science team to develop deep learning models based on ECG inputs - Tag datasets with high accuracy for AI model development - Curate disease codes, procedure codes, lab codes, etc from external or internal sources as needed - Review patient notes in Electronic Health Records (EHR) - Develop technically sound user stories by utilizing existing or in-progress apps **Qualifications Required:** - MBBS or higher qualification from a reputed institution in India **Requirements:** - Strong understanding of medicine with a focus on patient care, preferably in Cardiology, Internal Medicine, or ICU - Proficiency in programming languages like Python or R - Basic interpretation skills for ECGs - Strong interest in research and product development - Optional: Basic knowledge of Python, SQL, and biostatistics In this role, you will have the opportunity to work alongside brilliant minds in the field, contributing to research publications and solving real-world problems through Artificial Intelligence, Machine Learning, analytics, and insights derived from biomedical literature and large-scale datasets. Additionally, you have the chance to become a permanent part of the groundbreaking work at the forefront of biomedicine, as recognized by the Washington Post.,

Role Overview: As a Global Scientific Advisor at Novo Nordisk in the MedComm, Rare Disease Product and Portfolio Strategy department, you will be responsible for driving scientific communication, medical education, and cross-functional collaboration across Global Medical Affairs. Your role will involve developing and delivering high-quality, compliant scientific content, supporting global clinical and educational activities, and engaging with key opinion leaders to enhance scientific dialogue. You will lead medical communication strategies, support publication and medical education initiatives, and ensure alignment across medical affairs, medical excellence, and focus markets. Key Responsibilities: - Serve as a therapeutic-area expert across rare bleeding disorders, haemoglobinopathies, and rare endocrine conditions - Lead the development and critical review of scientific and omni-channel engagement materials, slide decks, graphical abstracts, and educational content to ensure scientific accuracy, medical appropriateness, and regulatory compliance - Provide internal medical guidance by prioritizing launch product timelines and ensuring accurate scientific data in communication materials - Drive strategic initiatives, mentor new team members, and identify opportunities for value creation and process improvements - Utilize and develop AI tools to enhance medical communication activities Qualifications: - MD or PhD with substantial clinical and/or research expertise in a relevant therapeutic area (e.g., Endocrinology, General Practice, or Internal Medicine). Additional education or professional experience in medical communication - Minimum 6 plus years of relevant experience in medical affairs and/or medical communications within the pharmaceutical or healthcare industry. Proven experience in clinical medicine, clinical research, and drug development - Demonstrated success in independently planning and executing global medical events (e.g., symposia, advisory boards, continuing medical education, and scientific programs) - Strong ability to influence and collaborate effectively with internal stakeholders and external experts at a global level - Expertise in developing high-quality, compliant scientific content - Excellent communication and interpersonal skills. Ability to work independently and make informed decisions - Familiarity with AI tools and their application in medical communication Kindly note that Novo Nordisk does not extend unsolicited employment offers and does not charge prospective employees with fees or make requests for funding as part of the recruitment process. The company is committed to an inclusive recruitment process and equality of opportunity for all job applicants.,