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Lead medical strategy for key therapeutic areas. Experience in clinical trials and regulatory affairs needed. **Key Responsibilities:** - Provide high-quality patient care. - Collaborate with cross-functional teams. - Ensure compliance with medical standards. - Maintain accurate patient records. **About the Role:** This is a key position within our growing team. We offer competitive compensation and opportunities for professional development.
About role & responsibilities • Provide primary and emergency medical care to patients • Diagnose illnesses and prescribe appropriate treatment • Maintain patient medical records and reports • Handle medical emergencies and first aid services • Support public health and preventive care programs • Ensure compliance with health and safety protocolsName of the PostsNo.of VacanciesQualificationMedical Officer 10MBBS Skills • Strong clinical assessment and diagnostic skills • Good patient-handling and communication skills • Emergency care and first aid management • Basic computer documentation skills Experience • Freshers and experienced MBBS candidates can apply Salary • ₹35,000 per month Benefits • Government health department employment • Stable job profile • Fixed monthly salary • No application fee Apply • Attend walk-in interview at the address mentioned in the official notification • Walk-in date: 02-01-2026 About the company • Chief Medical Officer, Bokaro is a government healthcare authority • Responsible for public health services and medical administration in Bokaro districtOfficial NotificationClick Here
About role & responsibilities • Deliver undergraduate and postgraduate medical/dental education • Conduct clinical teaching and academic mentoring • Participate in patient care and clinical services • Support research activities and academic publications • Contribute to departmental academic programs and CME activities • Maintain academic and administrative records • Participate in institutional development activitiesName of the PostsNo.of VacanciesQualificationAssistant Professor 18MBBS, BDS, MDS, MD/ MS Skills • Strong subject knowledge and teaching ability • Clinical decision-making and patient management • Research orientation and academic writing skills • Good communication and presentation skills Experience • As per AIIMS norms Salary • ₹1,01,500 per month (minimum) Benefits • Central government medical college employment • Competitive academic pay scale • Career growth and promotion opportunities • Teaching and research exposure Apply • Pay applicable application fee (UR/EWS/OBC: ₹1000; SC/ST/PwBD/Women: Nil) • Last date to apply: 21-01-2026 • Application start date: 22-12-2025 About the company • AIIMS Bhubaneswar is a premier central government medical institute • Provides advanced medical education, research and patient careOfficial Notification and Apply Online linkClick Here
About role & responsibilities • Provide medical consultation and primary healthcare services to students and staff • Diagnose illnesses and prescribe appropriate treatment • Maintain medical records and health reports • Handle medical emergencies and first aid services • Ensure implementation of health and safety protocols within the campus • Participate in health awareness and preventive care programs Qualification • MBBS Skills • Strong clinical assessment and diagnostic skills • Good communication and patient-handling ability • Basic computer and medical record documentation skills • Emergency care and first aid management Experience • Freshers and experienced MBBS candidates can apply Salary • ₹50,000 per month Benefits • Government institute employment • Stable and secure job profile • Fixed monthly salary • No application fee Apply • Send the completed form to the address mentioned in the official notification • Last date to apply: 15-01-2026 About the company • National Institute of Technology Meghalaya is a premier government engineering institute • Provides quality education and campus healthcare servicesOfficial Notification and Application FormClick Here
About Role & Responsibilities • Provide high-quality, patient-centered care for cardiology patients • Collaborate with multidisciplinary teams to ensure optimal patient outcomes • Participate in quality improvement initiatives and medical research • Ensure compliance with hospital policies and international medical standards Qualification • Board Certification in Cardiology • Western Qualification preferred Experience • 5+ years of experience in cardiology Skills • Cardiovascular medicine expertise • Patient care and management • Team collaboration • Research and quality improvement About the Company Cleveland Clinic Abu Dhabi is a world-class healthcare provider, offering comprehensive services in a state-of-the-art facility
About Role & Responsibilities • Lead daily clinical operations and provide high-quality patient care • Manage patient consultations, treatments, and follow-ups • Mentor junior staff and support their professional development • Participate in quality improvement and clinical audits to enhance patient services • Maintain accurate patient records and ensure compliance with health regulations Qualification • FRACGP (Fellow of the Royal Australian College of General Practitioners) • AHPRA (Australian Health Practitioner Regulation Agency) Registration Experience • Minimum 3 years of experience as a General Practitioner (GP) Skills • Strong clinical and diagnostic skills • Team leadership and mentorship • Knowledge of quality improvement processes About the Company Sonic HealthPlus is one of Australia’s leading healthcare providers, offering a wide range of medical services across various industries
About role & responsibilities • Act as scientific ambassador for oncology portfolio and provide non-promotional scientific exchange • Build and maintain peer-to-peer relationships with KOLs and healthcare professionals in oncology • Deliver balanced, evidence-based scientific information on oncology products and disease areas • Facilitate advisory boards, CMEs and scientific roundtables • Implement country-level medical affairs plans aligned with global strategy • Gather and synthesize field insights to support clinical development and lifecycle management • Support real-world evidence generation • Drive scientific support for oncology product launches • Train internal sales and marketing teams on disease state and product science • Develop educational content for healthcare professionals and internal stakeholders • Collaborate with Clinical Development, Regulatory, Market Access and Commercial teams • Ensure compliance with SOPs, ICH-GCP and local regulatory guidelines • Report adverse events and product complaints accurately Qualification • Advanced degree in Life Sciences – MBBS, MD, PhD or equivalent Skills • Strong knowledge of oncology, hematology and biomarkers • Excellent scientific communication and presentation skills • Ability to interpret and discuss clinical trial data • Strategic thinking and execution agility • Strong relationship-building with senior clinicians and thought leaders • Proficiency in MS Office and CRM tools • Understanding of Indian oncology treatment landscape and healthcare system Experience • Minimum 2+ years of experience as MSL or in Medical Affairs (Oncology) Benefits • Opportunity to work with a research-driven biopharmaceutical organization • Exposure to oncology clinical development and global medical affairs projects • Inclusive and collaborative work culture • Continuous learning and professional growth About the company • Research-driven biopharmaceutical company focused on innovative medicines and vaccines • Committed to world-class science, diversity, inclusion and patient-centric healthcare solutions
About role & responsibilities • Build and maintain scientific relationships with KOLs, HCPs and medical associations • Represent Turacoz at CMEs, conferences, webinars and scientific meetings • Deliver accurate and updated scientific information to healthcare professionals • Provide training to field teams and external speakers • Collect and communicate medical insights for strategy development • Collaborate with Medical, Marketing and Sales teams • Support clinical research initiatives and identify potential investigators • Ensure compliance with medical, ethical and regulatory guidelines Qualification • MBBS Skills • Strong scientific understanding of therapeutic areas • Excellent communication, presentation and relationship-building skills • Familiarity with ICH, GCP and medical governance practices • Data analysis and insight sharing ability • Proactive and adaptable with field-based work capability Experience • 0–2 years (Fresh MBBS graduates welcome) Benefits • Competitive compensation • Flexible/remote work options for select roles • Exposure to scientific communication and research projects • Professional growth and learning opportunities About the company • Turacoz is a medical communications company providing customized medical writing and scientific communication solutions • Offers publication, clinical research, regulatory writing, digital marketing and medical content development services • Conducts medical writing training workshops to promote ethical and accurate medical communication
About role & responsibilities • Work in Life Sciences R&D vertical supporting global pharmacovigilance operations • Create and manage ICSR case identification, data entry, MedDRA coding, case processing, submission and follow-ups • Monitor and assess safety of pharmaceutical products across clinical and post-marketing stages • Ensure compliance with global regulatory requirements and client guidelines • Analyse moderately complex safety data and develop appropriate solutions • Support detection, evaluation and prevention of adverse drug reactions • Manage small teams or work efforts when assigned • Collaborate with internal and client stakeholders • Work in rotational shifts as required Qualification • Bachelor of Pharmacy • Master of Pharmacy • MBBS Skills • Pharmacovigilance operations and ICSR processing • MedDRA coding and safety database management • Regulatory compliance knowledge • Analytical and problem-solving ability • Strong documentation and communication skills Experience • 7 to 11 years of experience in Pharmacovigilance / Drug Safety Salary • Salary Competitive (as per company standards) Benefits • Exposure to global life sciences and pharmacovigilance projects • Career growth and leadership opportunities • Professional and collaborative work environment About the company • Accenture is a global professional services company with strong capabilities in digital, cloud and security • Provides strategy, consulting, technology and operations services across 120+ countries • Serves global biopharma clients through advanced technology and intelligent operations centers
About role & responsibilities • Execute Medical Affairs strategy for CVRM products • Engage with healthcare professionals and scientific experts • Deliver scientific exchange and product education • Organize advisory boards, symposiums and medical events • Support real-world evidence and investigator studies • Gather and share actionable medical insights • Ensure compliance with PV, GxP and ethical standards Qualification • Master’s degree in scientific discipline • MD / PhD / PharmD preferred Skills • Strong scientific communication • Presentation and stakeholder engagement • Analytical and project management skills • Knowledge of pharmacovigilance and compliance Experience • Pharmaceutical / clinical research / medical affairs experience • Therapeutic area experience preferred Salary • Salary Competitive Benefits • Global medical affairs exposure • Career growth opportunities • Inclusive and collaborative culture About the company • AstraZeneca is a global science-led biopharmaceutical company • Focused on innovative medicines for serious chronic diseases • Operates across 100+ countries with strong R&D leadership
Key Responsibilities Act as scientific expert within franchise cross-functional teams Lead medical strategy, product ideation, evaluation, and regulatory scientific support Prepare SEC submissions, launch materials, CME and training content Review and approve promotional / non-promotional medical content Drive KOL engagement, advisory boards, medical education programs Support RWE studies, publications, and evidence generation Train sales and marketing teams on disease and product science Provide scientific responses to HCP and internal queries Represent Sun Pharma in internal and external scientific forums Eligibility & Experience MD Pharmacology 1–3 years experience as Medical Advisor / Sr. Medical Advisor Knowledge of ICH-GCP, Indian regulatory and ethics guidelines (MCI, UCPMP, DCGI) Strong research, scientific communication and medical writing skills Work Model Office-based (Mumbai) Travel: Less than 1 week per month
Key Responsibilities Lead and govern global PV safety systems, data marts, UAT and system validation Ensure data integrity, compliance, inspection readiness and regulatory reporting (PSUR, DSUR, PADER) Oversee EDC–Safety DB integrations and reporting solutions (QBE, dashboards) Drive automation, AI adoption and PV process innovation Develop SOPs, training programs and mentor teams Support audits, inspections and QPPV-delegated activities Required Skills & Experience Strong experience with Argus / ArisGlobal LifeSphere Knowledge of global PV regulations, SDLC and system validation Reporting tools: Cognos, Spotfire, Tableau; Oracle DB, PL/SQL, Python preferred Pharma / Health Authority experience mandatory Education Doctorate OR Master’s + 3 yrs OR Bachelor’s + 5 yrs OR Associate’s + 10 yrs OR High School + 12 yrs relevant experience
Role Summary Support global HEOR projects through economic modelling, evidence synthesis, and value assessments Key Responsibilities Support cost-effectiveness, budget impact and economic analyses Conduct literature searches and extract clinical, economic and epidemiology data Assist in building, adapting and maintaining health economic models Prepare model inputs, run analyses and document assumptions and results Support evidence synthesis, summary tables and technical report sections Contribute to value-for-money and HTA assessments Maintain data records related to modelling activities Prepare technical reports, presentations and slide decks Collaborate with epidemiology, market access and project teams Monitor timelines and proactively flag risks Required Qualifications Master’s degree in Economics, Biostatistics, Mathematics, Pharmacy, Public Health or related field 2–3 years’ experience in HEOR economic modelling (consulting/pharma preferred) Knowledge of health economics, HTA, decision modelling and epidemiology Strong data handling and interpretation skills Advanced Excel skills with VBA (mandatory) Basic knowledge of R and/or Python (preferred) Strong communication, teamwork and attention to detail Preferred Skills Hands-on experience in de novo and adapted health economic models Why Syneos Health Global exposure in HEOR & market access Inclusive, high-performance culture Strong career growth in healthcare analytics
Role Summary Support HEOR and RWE analytics teams in real-world evidence generation and statistical analysis Work on retrospective database studies and healthcare analytics projects Key Responsibilities Extract, clean, manipulate, and analyze healthcare data using SAS and R Analyze large US claims and EU EMR databases (CPRD, SNDS, etc.) Support design and execution of retrospective observational studies Apply regression, propensity scoring, and sensitivity analysis methods Create analytical tables, figures, and summaries for reports and manuscripts Support RWE reports, manuscripts, and presentations Translate analytical results into actionable insights for stakeholders Ensure timely delivery of project milestones Contribute to internal analytics process improvements Required Qualifications Master’s degree or higher in Biostatistics, Data Science, Epidemiology, Health Economics, or related field 2–3 years of HEOR/RWE analytics experience (consulting or pharma preferred) Proficiency in SAS and R Experience with US claims and EU EMR databases Strong communication and teamwork skills Preferred Skills Hands-on experience in RWE database analysis and statistical modeling Why Syneos Health Global CRO exposure Collaborative and inclusive culture Career growth in real-world evidence and analytics
About the Role Axtria is hiring experienced RWE analytics professionals to support global healthcare clients through advanced real-world data analytics, evidence generation, and strategic insights. This role blends healthcare analytics, machine learning, and consulting to improve clinical, medical, and commercial decision-making. Key Responsibilities Analyze large real-world healthcare datasets (claims, EHRs, patient charts) Perform retrospective database studies for RWE and R&D programs Apply advanced statistics and machine learning techniques Develop technical reports, SAPs, manuscripts, abstracts, and presentations Design studies and analytical strategies with cross-functional teams Present insights to internal and external stakeholders Manage project timelines, quality, and budgets Contribute to publications, conferences, and thought leadership Support innovative analytics (causal inference, GenAI, digital twins, etc.) Eligibility & Skills 3–8 years of experience in RWE analytics, healthcare data science, or consulting Strong knowledge of disease pathways and therapeutic areas Proficiency in SQL, Python, R, statistics, and data visualization tools Excellent communication, stakeholder management, and project leadership skills Bachelor’s in Life Sciences / Engineering / Statistics / OR Master’s in HEOR, Outcomes Research, Econometrics, or related field preferred Why Axtria Work with global pharma clients, cutting-edge AI/ML technologies, and a high-performance analytics culture focused on improving real-world patient outcomes
About Role & Responsibilities • Serve as a scientific peer-to-peer resource for disease experts and healthcare professionals • Engage in scientific discussions with key opinion leaders (KOLs) • Provide educational support and information on disease states and treatment modalities • Facilitate the exchange of scientific knowledge and research • Support the development of medical strategies Qualification • PhD, PharmD, or MD Experience • Experience in the pharmaceutical or medical industry preferred Skills • Strong scientific knowledge • Excellent communication and interpersonal skills • Ability to engage with KOLs and healthcare professionals Benefits • Health insurance • Paid time off • Continuing education support About the Company Novartis India is a global healthcare company that focuses on providing life-changing treatments across various therapeutic areas
Job ID: 25650 About the Role Execute medical affairs strategy in the assigned zone, driving scientific engagement, medical projects, and regulatory support to strengthen Boehringer Ingelheim’s diabetes portfolio. Key Responsibilities Engage with HCPs, attend scientific forums, and review literature to gather insights on therapy trends Deliver clear, non-promotional scientific communication to internal and external stakeholders Execute medical projects including IIS studies Support medico-marketing strategy implementation Identify and develop relationships with KOLs and expert experts (EEs) Provide medical support for product registrations, new indications, and defense of marketed products Prepare and review labeling and regulatory documentation Support regulatory affairs with expert access Eligibility Medical degree (Pharmacology preferred) or Life Sciences qualification 0–3 years pharma/healthcare experience (Fresh MD Pharmacology graduates can apply) 10+ years field experience acceptable for non-doctoral candidates Strong scientific knowledge in diabetes therapy area Good communication and MS Office skills
About Role & Responsibilities • Lead the medical affairs team to support the development and delivery of innovative medicines • Provide medical expertise in the development of marketing strategies • Collaborate with cross-functional teams to ensure medical alignment and compliance • Manage relationships with KOLs, researchers, and healthcare professionals • Ensure the adherence to regulatory standards and medical guidelines Qualification • Medical degree (MBBS/MD) or PhD in Life Sciences or related field Experience • 5+ years of experience in medical affairs, with leadership experience Skills • Strong leadership and team management skills • In-depth knowledge of medical affairs processes • Excellent communication, presentation, and interpersonal skills About the Company Dr. Reddy's Laboratories is a global pharmaceutical company dedicated to providing affordable and innovative medicines
About Role & Responsibilities • Lead and oversee the medical affairs department's operations • Provide strategic and medical expertise to support business goals • Work closely with cross-functional teams to align on medical strategies • Manage relationships with key opinion leaders (KOLs), regulatory bodies, and healthcare professionals • Ensure regulatory compliance in all medical activities and interactions Qualification • Medical degree (MBBS/MD) or PhD in Life Sciences or related fields Experience • 4+ years of experience in medical affairs with leadership or consultancy roles Skills • Strong leadership and team management skills • Excellent communication and collaboration skills • In-depth understanding of regulatory standards and medical practices About the Company Dr. Reddy's Laboratories is a multinational pharmaceutical company focused on providing high-quality, affordable medicines
About Role & Responsibilities • Manage clinical trial documentation • Perform clinical data analysis and reporting • Ensure protocol compliance • Support audits and inspections Qualification B.Pharm / M.Pharm / Pharm.D / MSc / BSc Experience 0–3 years Skills • Clinical data management • Documentation • MS Excel & reporting About the Company TRDFIN provides clinical research and data management services to pharma companies