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Role & Responsibilities • Review published biomedical literature for identification of adverse reaction case reports and non-individual case reports • Apply regulatory and internal guidance to determine case validity and reportability • Perform relevancy assessment based on accepted pharmacovigilance guidelines • Provide training and guidance to literature scanners on inclusion criteria • Collaborate with subject matter experts to ensure team capability and compliance • Perform additional pharmacovigilance tasks as assigned by lead or manager Qualification • MBBS or MD Experience • 0–3 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of global PV regulatory guidelines • Narrative writing and medical case assessment • MedDRA coding proficiency • Understanding of pharmacological concepts About the Company Wipro is a leading global information technology, consulting, and business process services company that delivers innovation-led solutions to clients across industries, including life sciences and healthcare. With a strong presence worldwide, Wipro supports pharmaceutical organizations in ensuring drug safety, regulatory compliance, and patient-centric healthcare delivery.Interested candidates can share their resumes at varsha.kamalapurkar@wipro.com

Role & Responsibilities • Lead therapeutic area (TA) medical strategy and act as core scientific member of cross-functional franchise team • Plan and execute medical affairs strategy including publications, medical education, research, and patient support programs • Engage Key Opinion Leaders and Thought Leaders for scientific exchange and advisory activities • Drive regional medical affairs execution including product education and special projects • Provide scientific training and medical insights to sales and marketing teams • Serve as TA scientific expert for interpretation and communication of clinical and real-world data • Ensure compliance with Indian regulations, UCPMP, MCI code, and Drugs & Cosmetics Act • Support development of long-term medical affairs strategic plans Qualification • MBBS with MD (Pharmacology/Medicine) or full-time postgraduate medical qualification Experience • 2–4 years as Medical Advisor in pharmaceutical or research organizations Skills • Strong therapeutic area knowledge and research methodology understanding • Medical writing and clinical trial knowledge (ICH-GCP preferred) • Strategic thinking and scientific communication skills • Regulatory compliance knowledge (Indian regulations) • Excellent stakeholder engagement and presentation abilities About the Company Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company operating in 66 countries, driven by the purpose “Good Health Can’t Wait.” With strong R&D, manufacturing, and commercial presence, Dr. Reddy’s focuses on access, affordability, and innovation to serve over 1.5 billion patients worldwide by 2030 while maintaining sustainability, integrity, and people-centric work culture.

Role & Responsibilities • Perform medical review of company, literature, and regulatory ICSRs • Select and assess adverse events for seriousness and expectedness • Conduct MedDRA coding review of adverse events • Review causality assessments and perform label assessment • Classify product role (suspect, concomitant, interacting) • Review medical history, concomitant conditions, and laboratory data • Evaluate case narratives for medical accuracy and completeness • Perform medical review and quality review of aggregate safety reports (PSURs, PADERs) • Conduct medical review of Risk Management Plans (RMPs) • Review Signal Management Reports and support signal evaluation Qualification • MBBS or MD (Pharmacology preferred) Experience • Relevant experience in pharmacovigilance medical review or drug safety preferred Skills • Strong knowledge of pharmacovigilance regulations and safety reporting standards • MedDRA coding proficiency • High attention to clinical detail and document quality • Strong written and verbal communication skills • Ability to work with global safety documentation and regulatory timelines About the Company The hiring organization operates in regulated pharmacovigilance and drug safety domains, supporting global pharmaceutical safety surveillance, aggregate reporting, and risk management activities aligned with international regulatory standards.

Role & Responsibilities • Support and conduct biomedical and biotechnology research projects • Assist in experimental design, data collection, and analysis • Prepare research documentation, reports, and scientific manuscripts • Maintain laboratory records and ensure compliance with research protocols • Coordinate with project investigators and multidisciplinary research teams • Ensure proper handling of laboratory equipment, samples, and reagents • Participate in project meetings, audits, and review activitiesName of the PostsNo.of VacanciesQualificationResearch Associate03MD/MS MDS, BDS/M.Pharm, M.V.Sc, M.E/ M.Tech Experience • Research exposure in biomedical, biotechnology, or related domains preferred • Fresh or experienced candidates eligible as per NABI norms Skills • Laboratory research and experimental handling • Data analysis and scientific documentation • Understanding of research methodologies and protocols • Attention to detail and regulatory compliance • Team coordination and communication About the Company The National Agri-Food Biotechnology Institute (NABI) is an autonomous research institute under the Department of Biotechnology, Government of India, dedicated to cutting-edge research in agri-food biotechnology, nutrition, and translational sciences aimed at improving national food security and public health.Date of Walk-in-Interview08-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Provide inpatient and outpatient medical care under the supervision of senior consultants • Diagnose, treat, and manage patients as per institutional protocols • Participate in ward rounds, emergency duties, and clinical procedures • Maintain accurate patient records and clinical documentation • Assist in teaching undergraduate and postgraduate students • Support departmental research, audits, and academic activities • Ensure adherence to hospital policies, ethical standards, and patient safety normsName of the PostsNo.of VacanciesQualificationSenior Resident 10MD/MS, DNB, Post-Graduation Experience • Fresh or experienced postgraduates eligible as per IGIMS norms • Clinical residency exposure preferred Skills • Strong clinical decision-making ability • Patient assessment and case management • Medical documentation and record-keeping • Team collaboration and communication • Ability to work in a hospital-based clinical environment About the Company Indira Gandhi Institute of Medical Sciences (IGIMS), Patna is a premier government medical institute committed to delivering advanced tertiary healthcare, medical education, and research, serving as a major referral center for Bihar and neighboring regions.Date of Walk-in-Interview07-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Perform dental examinations, diagnosis, and routine oral procedures • Repair, extract, and restore damaged teeth • Fill cavities and perform root canal treatments • Develop and implement patient-specific treatment plans • Prescribe and administer medications for pain management and infection control • Evaluate dental X-rays and oral health conditions • Educate patients on oral hygiene and preventive dental care • Measure, fit, and place dental appliances • Refer patients to specialists when required Qualification • BDS (Bachelor of Dental Surgery) Experience • Minimum 4+ years of clinical dental experience • RCT experience preferred Skills • Clinical dentistry and oral surgery skills • Diagnosis and treatment planning • Patient communication and counseling • X-ray interpretation and documentation • Time management and chairside efficiency About the Company The hiring dental clinic in Hyderabad is a growing healthcare facility committed to delivering quality oral care services with a patient-centric approach, providing modern dental treatments in a professional clinical environment.

Role & Responsibilities • Deliver undergraduate and postgraduate medical teaching as per NMC curriculum • Conduct lectures, practical sessions, clinical postings, and assessments • Guide and mentor students in academic and clinical training • Participate in research activities and publications • Maintain academic records, attendance, and internal assessments • Support departmental academic planning and development • Assist in curriculum updates, examinations, and accreditation activitiesName of the PostsVacanciesEducationAssistant Professor220MD / MS , DNB, Post-graduation Experience • As per NMC / APMSRB norms Skills • Teaching and academic mentoring skills • Strong clinical knowledge in the specialty • Communication and presentation skills • Research and documentation abilityOC Candidates: Rs. 2,000/-BC, SC, ST, EWS, PWD Candidates: Rs. 1500/. About the Company Andhra Pradesh Medical Services Recruitment Board (APMSRB) is the official government body responsible for recruiting qualified medical faculty to strengthen teaching hospitals and medical colleges across Andhra Pradesh.Starting date08-01-2026Closing date22-01-2026 Official NotificationClick Here

Role & Responsibilities • Provide Unani medical consultation and treatment to patients • Diagnose illnesses and prescribe Unani medicines • Maintain patient case records and treatment documentation • Educate patients on diet, lifestyle, and preventive healthcare • Participate in government health programs and camps • Ensure adherence to clinical protocols and public health guidelines Qualification • MBBS / BUMS Experience • Freshers and experienced candidates Skills • Clinical diagnosis and patient management • Knowledge of Unani medicine principles • Good communication and documentation skills About the Company Madhya Pradesh Public Service Commission (MPPSC) is the state recruiting authority responsible for appointing qualified healthcare professionals to strengthen government healthcare services across Madhya Pradesh.Starting date13-03-2026Closing date12-04-2026Official NotificationClick Here

Role & Responsibilities • Provide outpatient and primary medical consultation to ECHS beneficiaries • Diagnose, treat and manage common medical conditions • Prescribe medications and ensure rational drug use • Maintain patient medical records and documentation • Refer patients to specialists when required • Participate in health screening and preventive programsName of the PostsVacanciesEducationMedical Officer47MBBS, MD/MS Experience • Freshers or experienced medical professionals Skills • Strong clinical diagnosis and patient care skills • Good communication and documentation skills • Ethical medical practice and decision making About the Company The Ex-Servicemen Contributory Health Scheme (ECHS) is a Government of India healthcare organization providing comprehensive medical care to ex-servicemen and their dependents through a nationwide network of polyclinics and empanelled hospitals.Starting date02-01-2026Closing date28-01-2026Official NotificationClick HereApplication FormClick Here

Role & Responsibilities • Oversee pharmacovigilance vendors and CRO partners in a sponsor environment • Review, manage and approve SAEs, SUSARs and ICSR submissions • Support preparation and medical review of DSURs and aggregate safety reports • Provide safety input into clinical protocols, Investigator’s Brochures and trial documents • Coordinate with Clinical Operations, QA and Regulatory Affairs teams • Support inspection readiness, audits and safety governance meetings • Manage long-term follow-up and safety activities specific to Cell & Gene Therapy trials • Ensure compliance with ICH-GCP, ICH E2 and global PV regulations Qualification • Degree in Pharmacy, Life Sciences or related discipline Experience • Experience in Pharmacovigilance and Clinical Trials • Prior exposure to sponsor oversight or CRO/vendor management preferred Skills • Strong understanding of clinical safety reporting and PV regulations • Ability to work in cross-functional sponsor teams • Good documentation, coordination and communication skills • Exposure to Cell & Gene Therapy, Oncology or Rare Disease programs preferred About the Company This is a growing sponsor organization focused on developing innovative Cell & Gene Therapy programs, driving advanced clinical research with strong regulatory compliance and patient safety governance at its core.

Role & Responsibilities • Review high-value and complex medical claims for up-coding, unbundling, duplication, and misrepresentation • Prevent fraudulent, abusive, and non-compliant claim payments • Apply CPT and diagnosis coding knowledge during claim investigations • Ensure compliance with CMC guidelines, benefit plans, and client-specific policies • Identify provider aberrant behavior and risk patterns • Support reporting, audits, and special investigative projects • Maintain adherence to state and federal healthcare regulations Qualification • BPT / MPT • BHMS / BAMS / BUMS • BDS / B.Sc Nursing (minimum 1 year corporate experience mandatory) Experience • 6 months – 4 years in healthcare, claims review, or medical auditing roles Skills • Strong analytical and investigation skills • Understanding of healthcare documentation and billing systems • High attention to detail and quality orientation • Good communication and reporting skills About the Company Optum is a global healthcare and analytics organization delivering data-driven insights, technology, and services to improve healthcare quality, efficiency, and patient outcomes worldwide.

Role & Responsibilities • Collect, assess, and investigate adverse events, product malfunctions, and complaints related to medical devices • Prepare and submit MDV reports to CDSCO, US FDA, and EU authorities • Maintain documentation for recalls, FSCAs, risk assessments, and CAPA implementation • Handle end-to-end complaints management and audit support • Monitor and report ADRs from spontaneous reports, literature, and clinical trials • Prepare and submit ICSRs, PSURs, and DSURs • Perform signal detection, trend analysis, and risk–benefit assessments • Execute Post-Marketing Surveillance (PMS) activities • Ensure compliance with global PV and MV regulatory requirements Qualification • B.Pharm / M.Pharm Experience • 1–6 years in Pharmacovigilance or Medical Device Vigilance Skills • Strong knowledge of global PV and MDV regulations • ICSR, PSUR, DSUR preparation • Complaints handling and CAPA management • Audit readiness and regulatory compliance • Good communication and documentation skills About the Company Appasamy is a leading medical device and pharmaceutical organization known for its high-quality ophthalmic products and strong commitment to patient safety, regulatory compliance, and innovation in healthcare solutions.

Role & Responsibilities • Provide medical oversight for clinical trials • Review safety data and adverse events • Ensure protocol compliance Qualification • MD Pharmacology Experience • Fresher Skills • Safety evaluation, clinical judgment, documentation About the Company Cliantha Research is a global CRO conducting multinational clinical trials.

Role & Responsibilities • Perform medical review and approval of post-marketing ICSRs and clinical trial SAE reports • Assess seriousness, expectedness, causality and coding accuracy of safety cases • Prepare company medical comments, follow-up queries and similar event analysis • Complete and maintain safety trackers and supporting documentation • Support the Qualified Person for Pharmacovigilance in evaluation of safety issues • Review and provide medical input into periodic safety reports • Review literature screening strategies and evaluate articles for safety case identification • Contribute to medical evaluation of safety signals and ongoing risk assessment Qualification • MD (Doctor of Medicine) Experience • Open to Medical Doctors seeking entry or early-career growth in pharmacovigilance Skills • Strong understanding of pharmacovigilance principles and safety reporting • Ability to plan, organize, prioritize and manage multiple safety tasks • Excellent written and verbal English communication (minimum B2 level) • Strong presentation and documentation skills • Advanced proficiency in MS Office tools • Ability to work effectively across cultures and cross-functional teams About the Company PrimeVigilance is a global pharmacovigilance and regulatory affairs organization with operational presence across North America, Europe and Asia, supporting pharmaceutical and biotech companies with end-to-end drug safety, medical information and risk management services.

Role & Responsibilities • Author, manage and lead development of regulatory medical writing documents for global and domestic submissions • Prepare protocols, clinical study reports, investigator brochures, briefing documents, IND/NDA/MAA and regulatory response documents • Collect, evaluate and integrate cross-functional scientific data into showing cohesive submission strategies • Plan, outline, write, review, coordinate approvals and finalize regulatory documents • Conduct document initiation and comment-resolution meetings for stakeholder alignment • Ensure accuracy, consistency and scientific integrity across related documents • Perform quality checks, peer reviews and maintain audit-ready documentation • Coordinate scientific reviews and manage timelines and delivery risks • Maintain therapeutic area knowledge and regulatory guideline updates • Provide coaching, support metrics tracking and contribute to process improvements • Maintain training records and support vendor coordination when required Qualification • Doctoral or Post-Graduate degree in Life Sciences / Pharmacy or clinical degrees (MBBS / BDS / BAMS / BHMS etc.) • Advanced degree (MD / PhD) preferred Experience • Minimum 3+ years of experience in regulatory medical writing with leadership exposure Skills • Strong knowledge of ICH, global regulatory guidelines and pharma industry standards • Excellent scientific writing, documentation and editing skills • Strong project management, decision-making and risk-mitigation abilities • Excellent communication, stakeholder management and interpersonal skills • Innovative, detail-oriented and adaptable working approach About the Company Sun Pharmaceutical Industries Ltd (SPIL) is India’s largest pharmaceutical company and a leading global specialty generics organization with a strong R&D-driven culture delivering high-quality, affordable medicines across more than 100 countries.

Role & Responsibilities • Engage with Thought Leaders (Doctors) to exchange and disseminate scientific, educational and research-based information • Conduct proactive on-label and reactive off-label scientific discussions in line with regulatory guidelines • Respond to medical and scientific queries from Medical Societies regarding company products • Organize, support and participate in advisory board meetings • Attend congresses and conventions to network with key stakeholders and gather competitive intelligence • Plan and coordinate scientific education programs and training sessions within assigned therapeutic areas • Identify, profile and segment Thought Leaders and develop engagement strategies aligned with Medical Affairs plans • Prepare activity reports and track performance against objectives • Provide additional external scientific training and educational support as required Qualification • Degree in natural sciences or medical background (MD / MBBS / BAMS / BDS / MDS) Experience • Experience in Medical Affairs or MSL roles preferred • Prior exposure to pharmaceutical or clinical research environment preferred Skills • Basic understanding of therapy areas and related molecules • Knowledge of clinical trial design and rationale • Strong presentation, written and verbal communication skills • Ability to work independently and collaboratively • Relationship-building and stakeholder management skills About the Company Bayer is a global life science company operating in the healthcare and agriculture sectors, committed to delivering innovative solutions that improve health outcomes and quality of life worldwide.

Role & Responsibilities • Perform medical review of adverse events for investigational and marketed products • Assess and interpret ICSRs using MedDRA and safety databases such as ARGUS • Ensure compliance with global pharmacovigilance regulations and SOPs • Provide medical input for PSURs, PADERs and other aggregate safety reports • Identify, evaluate and manage potential safety signals • Liaise with client safety and medical teams for case assessments • Maintain medical surveillance of clinical and post-marketing safety data • Support mentoring and training of pharmacovigilance staff • Maintain ongoing medical education in drug safety and clinical development Qualification • MD / MBBS / DO from a recognized institution • Completed accredited residency Experience • 1–2 years of clinical practice experience preferred • Minimum 1 year experience in pharmacovigilance / pharmaceutical or biotechnology industry preferred Skills • Strong knowledge of global pharmacovigilance regulations • Proficiency with MedDRA, ARGUS and safety databases • Excellent written and verbal communication skills • Strong analytical and risk assessment abilities • Proficiency in MS Word, Excel, PowerPoint and safety systems • Ability to collaborate across cross-functional teams About the Company Syneos Health® is a global, fully integrated biopharmaceutical solutions organization operating across more than 110 countries. With over 29,000 employees, Syneos Health supports clinical development, medical affairs and commercialization for pharmaceutical and biotech companies, having contributed to the majority of recent FDA and EMA-approved therapies worldwide.

Key Responsibilities • Lead and support development of AMCP Dossiers (Format v5.0) • Perform targeted literature searches and structured evidence summaries • Prepare disease burden, epidemiology, unmet need and value narratives • Support HE economic model inputs and burden-of-illness assessments • Develop Global Value Dossiers (GVDs), reimbursement dossiers & payer slide decks • Translate complex clinical and economic evidence into payer-friendly content • Manage timelines and deliverables in a consulting environment • Collaborate with HEOR, market access and evidence generation teams • Provide quality oversight and mentoring to junior writersEssential Requirements • Master’s degree or higher in Public Health / Health Economics / Pharmacy / Epidemiology / Life Sciences • 5+ years HEOR / Market Access writing experience • Strong knowledge of cost-effectiveness, payer evidence & reimbursement strategy • Excellent scientific writing and communication skills • Ability to manage multiple client deliverables in fast-paced projectsPreferred Qualifications • Hands-on AMCP dossier development experience • Experience with Global Value Dossiers (GVDs) • Manuscript writing and publication experienceWhy Join Syneos Health • Global exposure in U.S. market access programs • Work with cross-functional clinical & commercial teams • High-impact HEOR & reimbursement strategy projects • Accelerated professional growth in life sciences consulting

Key Responsibilities • Coordinate and monitor ongoing research project activities • Assist in planning, implementation, and documentation of research protocols • Ensure compliance with institutional ethics committee and regulatory guidelines • Support clinical data collection, verification, and reporting • Liaise with investigators, research staff, and administrative departments • Prepare project reports, summaries, and documentation • Support audit, monitoring, and regulatory inspections • Maintain accurate project records and documentationEligibility Criteria Qualification: MBBS (Mandatory) Age Limit: Minimum: 21 Years Maximum: 35 Years About the Organisation All India Institute of Medical Sciences (AIIMS), Rishikesh is a premier government medical institute dedicated to excellence in healthcare delivery, medical education, and biomedical research. The institute is inviting applications for the position of Project Coordinator to support institutional research initiatives.Last Date of Application16-01-2026Official NotificationClick Here