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Role & Responsibilities • Perform medical review and clinical assessment of ICSRs in safety databases • Verify adverse event selection, seriousness, MedDRA coding, causality, labeling, narratives and company clinical comments • Handle medical queries, literature screening and safety database follow-ups • Ensure compliance with ICH, EMA, GVP and GCP guidelines • Mentor and train PV associates on safety conventions and event capturing • Support literature surveillance, signal detection and risk management activities • Review and prepare PSURs, PBRERs and Risk Management Plans (RMPs) • Participate in audits, inspections and global pharmacovigilance collaboration Qualifications & Experience • MBBS (PG degree preferred) • Minimum 3 years of Pharmacovigilance / Drug Safety experience Skills • Strong knowledge of global PV regulations (ICH, EMA, GVP, GCP) • Excellent communication and documentation skills • Ability to manage complex safety cases and work in regulated environments • Experience with safety databases and literature surveillance About the Company • Cencora is a global healthcare services organization dedicated to creating healthier futures worldwide. • The company supports pharmaceutical and life sciences organizations with end-to-end drug safety, regulatory, and clinical solutions.
Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) for seriousness, causality, labeling and MedDRA coding • Ensure accurate and timely safety case processing in line with global regulatory timelines and client SOPs • Review source documents and narratives for medical accuracy and database consistency • Write company causality comments and route cases through workflows as per SOPs • Validate E2B reporting and perform self-quality checks before case finalization • Lead internal and cross-functional trainings and mentor team members • Handle medical assessment queries, case follow-ups and regulatory clarifications • Support PV compliance, audits, inspections, documentation archiving and process transitions Qualifications & Experience • MBBS / MD • 7–11 years of experience in Pharmacovigilance / Drug Safety medical review Skills • Strong medical writing and safety narrative skills • Expertise in MedDRA, WHO-Drug, ICSR processing and global PV regulations • Proficiency in safety databases and MS Office • Excellent English communication skillsAbout the Company • Accenture is a leading global professional services company specializing in strategy, consulting, digital, technology, and operations.
Role & Responsibilities • Lead and implement HEOR strategies to support market access for Diabetes and Obesity brands • Drive evidence generation including economic models, cost-effectiveness, QoL and outcomes studies • Develop payer value stories and contribute to global reimbursement dossiers • Support affiliates for reimbursement and HTA submissions • Lead publication strategies for abstracts, posters, and peer-reviewed journals • Build and manage global stakeholder networks across healthcare, pharma, and academia • Deliver internal and external HEOR training and scientific presentations • Collaborate on retrospective and prospective real-world and clinical research studies Qualifications & Experience • Master’s degree in Health Economics, Outcomes Research, Epidemiology, Biostatistics, or related field • Minimum 6 years of HEOR experience (pharma/consulting preferred) • Proven publication track record Skills • Strong strategic planning and market access knowledge • HE modeling, HTA, and payer evidence generation expertise • Excellent communication and stakeholder management skills About the Company • Novo Nordisk is a global healthcare leader in Diabetes and Obesity care, driving long-term health impact through innovationHow to Apply • Apply online before 22-01-2026
Role & Responsibilities • Provide comprehensive OPD and IPD cardiology consultations and treatments • Manage cardiovascular emergencies and provide on-call coverage • Diagnose, treat, and follow up on cardiac patients • Maintain accurate medical records and clinical documentation • Ensure compliance with clinical governance and quality standards • Participate in continuous quality improvement and professional development activities • Collaborate with multidisciplinary teams for patient care Qualifications & Experience • Basic medical degree with recognized cardiology specialty qualification • Minimum 3–5 years post-qualification experience at Specialist level • At least 1 year Specialist experience from Tier 1 country (as per UAE norms) • Eligibility for UAE healthcare authority registration • Valid life support certifications (BLS, ACLS, PALS, ATLS, NRP) Skills • Strong cardiology clinical expertise and emergency handling skills • Excellent documentation and patient communication abilities • Knowledge of UAE clinical governance and regulatory standards About the Company • NMC Healthcare is a leading private healthcare provider in the UAE delivering advanced medical and surgical services
Role & Responsibilities • Provide primary medical care to industrial employees • Conduct occupational health assessments and fitness-for-duty evaluations • Manage workplace injuries and on-site medical emergencies • Ensure compliance with occupational health and safety regulations • Maintain accurate medical records and clinical reports Qualifications & Experience • MBBS with valid medical license • Minimum 3 years of occupational health experience Skills • Industrial healthcare and emergency response • Strong documentation and compliance management • Good communication and clinical assessment skills About the Company • Aster DM Healthcare is a leading international healthcare provider delivering comprehensive medical services across the GCC
Role & Responsibilities • Provide comprehensive OPD consultations and patient-centered primary care • Diagnose and manage acute and chronic medical conditions • Deliver preventive care, health screenings, and immunizations • Educate patients on disease management and medication adherence • Coordinate with specialists for complex case management • Maintain accurate electronic medical records and documentation • Participate in community health and wellness initiatives Qualifications & Experience • MBBS from a recognized institution • Minimum 4 years of primary care clinical experience • Valid medical registration Skills • Strong diagnostic and clinical decision-making abilities • Excellent patient communication and counselling skills • Ability to work within multidisciplinary healthcare teams About the Company • A confidential healthcare organization in Dubai delivering comprehensive primary care services
Role & Responsibilities • Provide OPD and IPD consultations and specialized treatments in assigned specialty • Diagnose, manage, and follow up on acute and chronic medical conditions • Perform specialty-specific procedures and surgeries • Participate in emergency duties and multidisciplinary case management • Maintain accurate clinical documentation and patient records • Adhere to hospital protocols, safety standards, and MOH Oman regulations Specialties Required • Nephrology • Gastroenterology • Cardiac Surgery • Pediatric Cardiology • Pediatric Ophthalmology • Hematology • Obstetrics & Gynecology • General Surgery • Urology • Neurology • General Practitioner • Ophthalmology (Corneal Transplant) • Interventional Radiology Qualifications & Experience • Specialist: MBBS + MD/MS (Age ≤ 45 years) • Consultant: MBBS + MD/MS + MCh (Age ≤ 50 years) • Minimum 3–8 years of clinical experience Skills • Strong specialty-specific clinical expertise • Patient communication and multidisciplinary coordination • Emergency and critical care handling skills Salary • ₹10,00,000 – ₹15,00,000 per month (approx.) About the Company • Ministry of Health Oman is a government healthcare authority delivering advanced medical services across Oman
Role & Responsibilities • Conduct comprehensive dermatological evaluations and diagnoses • Perform advanced dermatology procedures including laser therapy and Mohs surgery • Develop personalized treatment plans based on patient needs • Educate patients on skin care, prevention, and treatment usage • Collaborate with multidisciplinary teams for complex case management • Maintain accurate clinical documentation and patient records • Participate in clinical research and mentor junior staff • Support community outreach and dermatology awareness programs Qualifications & Experience • MD/MS in Dermatology from a recognized institution • Board certification in Dermatology • Minimum 5 years of clinical dermatology experience Skills • Expertise in advanced dermatology procedures • Strong diagnostic, analytical, and patient communication skills • Attention to detail and documentation accuracy Salary • AED 40,000 – 45,000 per month About the Company • Zulekha Hospital is a leading multi-specialty hospital in the UAE delivering advanced dermatology and cosmetic care
Role & Responsibilities • Coordinate with Patient Relations, Nursing, Physicians, Finance, and external stakeholders to ensure smooth insurance formalities • Monitor and follow up on prior authorizations for OPD and IPD services • Conduct claims analysis, audits, and reconciliations with insurance companies • Ensure compliance with insurance company requirements and hospital policies • Identify issues, analyze problems, and implement effective resolutions • Maintain accurate documentation and prioritize departmental requirements Qualifications & Experience • Bachelor’s Degree (Medical preferred) • 2–4 years of experience in insurance coordination, medical claims, or hospital operations Skills • Strong leadership and relationship management skills • Excellent English communication and documentation abilities • Good analytical, organizational, and MS Office skills • Understanding of hospital operations and insurance workflows About the Company • American Hospital Dubai is a leading private hospital delivering world-class medical services in the UAE
Role & Responsibilities • Provide inpatient and outpatient clinical care under consultant supervision • Perform patient assessments, treatment planning, and clinical procedures • Participate in ward rounds, emergency duties, and clinical documentation • Assist in diagnosis, management, and follow-up of patients • Support academic, teaching, and research activities • Ensure adherence to hospital policies, safety protocols, and clinical standards Qualifications & Experience Name of the PostsNo.of VacanciesQualificationSenior Resident 49MBBS/MD/MS, DNB, M.Sc, Any Degree, Post Graduation, Ph.D Skills • Strong clinical decision-making and patient management skills • Good communication and documentation abilities • Ability to work in emergency and hospital care environments About the Company • ESIC (Employees’ State Insurance Corporation) is a central government healthcare organization delivering medical services and academic training across IndiaDate of Walk-in-Interview20-01-2026Official Notification and Application FormClick Here
Role & Responsibilities • Provide OPD and IPD consultations and treatment • Diagnose and manage acute and chronic medical conditions • Participate in emergency duties and health programs • Maintain clinical documentation and patient records Qualifications & Experience • MBBS with valid medical registration Skills • Clinical assessment and patient management • Good communication and documentation skillsAbout the Company • ECHS (Ex-Servicemen Contributory Health Scheme) provides healthcare services to ex-servicemen and their dependentsLast Date of Application28-01-2026Official NotificationClick Here
Role & Responsibilities • Provide OPD and IPD medical consultations and treatment • Diagnose and manage acute and chronic medical conditions • Participate in emergency duties and health programs • Maintain patient records and clinical documentation Qualifications & ExperienceName of the PostsVacanciesEducationMedical Officer35MBBS• MBBS with valid medical registration Skills • Clinical assessment and patient management • Good communication and documentation skills Salary • Up to ₹60,000 per monthAbout the Company • CMOH Murshidabad is a government health authority providing public healthcare services in West BengalApplication last date30-01-2026 Official NotificationClick Here
Role & Responsibilities • Support clinical and biomedical research activities under project guidelines • Perform patient evaluation, data collection, and documentation • Assist investigators in study coordination and reporting • Ensure compliance with research protocols and ethical standards Qualifications & Experience • MBBS / B.V.Sc / BDS • Valid professional registration Skills • Clinical research knowledge • Good documentation and analytical skills How to Apply • Attend the walk-in interview on 20-01-2026 at: Department of Pediatrics, AIIMS Bibinagar, Hyderabad, Telangana – 508126Official Notification and Application FormClick Here
Role & Responsibilities • Provide OPD and IPD gynecological consultations and treatments • Conduct antenatal, postnatal, and women’s health services • Perform gynecological procedures and assist in deliveries • Maintain patient records and clinical documentation • Participate in emergency duties and departmental activitiesQualifications & ExperienceName of the PostsVacanciesEducationGynecologist02 MBBS with MD/MS/Diploma Skills • Clinical decision-making and patient counselling • Knowledge of women’s healthcare proceduresAbout the Company • JMC is a government medical organization providing public healthcare services and employment opportunitiesApplication last date23-01-2026Official NotificationClick HereApply OnlineClick Here
Role & Responsibilities • Support clinical and biomedical research activities • Conduct data collection, patient evaluation, and documentation • Assist in study coordination and reporting • Ensure adherence to research protocols and ethical guidelines Qualifications & Experience • MBBS degree • Valid medical registration Skills • Clinical research knowledge • Good documentation and analytical skills Salary • Up to ₹67,000 per month How to Apply • Submit filled application form to: SVIMS-Sri Padmavati Medical College for Women, Tirupati, Andhra Pradesh – 517501Address: SVIMS-Sri Padmavati Medical College for Women, Tirupati, Andhra Pradesh, 517501. Official NotificationClick HereApplication FormClick Here
Role & Responsibilities • Provide inpatient and outpatient clinical care under departmental supervision • Perform patient assessments, treatment planning, and clinical procedures • Assist consultants in diagnosis, management, and follow-up of patients • Participate in ward rounds, emergency duties, and clinical documentation • Support departmental academic and research activities • Ensure adherence to hospital policies, clinical protocols, and safety standardsName of the PostsNo.of VacanciesQualificationSenior Resident 02Post-Graduation , DNB Skills • Strong clinical assessment and decision-making skills • Good communication and documentation abilities • Ability to work in hospital and emergency care settings Salary • ₹1,27,260 – ₹1,38,600 per month How to Apply • Attend the walk-in interview at: Homi Bhabha Cancer Hospital & Research Centre, Plot No. 1, Medicity, New Chandigarh, Punjab 140901 About the Company • Tata Memorial Centre (TMC) is a premier oncology institute delivering advanced cancer care, education, and research in IndiaOfficial NotificationClick Here
About the Role & Responsibilities • Perform medical verification and processing of cashless health insurance claims • Review medical documents, treatment details, and hospital bills • Handle email-based medical queries and provide claim clarifications • Maintain accurate documentation and prepare reports • Ensure compliance with insurance and medical review guidelines Qualification • BHMS / BDS Experience • Experience in cashless insurance claims preferred • Freshers are also eligible Skill • Medical documentation review • Basic insurance claim processing knowledge • Email communication and reporting • Attention to detail and accuracy • Time management About the Company • Vidal Health is a leading healthcare and insurance administration company providing claims management and healthcare services across IndiaNote - Local candidates Will be Preferred
Role & Responsibilities: • Prepare, compile, and submit regulatory dossiers for pharmaceutical export registrations to global regulatory authorities • Maintain CTD/eCTD documentation for product registrations, renewals, variations, and post-approval changes • Ensure compliance with international regulatory requirements and current guidelines across export markets • Act as a liaison with regulatory agencies, export authorities, and external consultants for submission queries and follow-ups • Coordinate with internal teams including QA, QC, Production, R&D, and Supply Chain to collect required technical documentation • Track submission timelines, monitor status, and respond to deficiency letters within defined timelines • Maintain organized regulatory databases, files, and documentation as per regulatory and company standards • Provide regulatory intelligence on evolving global regulations impacting pharmaceutical exports • Support labeling, packaging, and artwork compliance as per importing country requirements Qualification: • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, or a related discipline Experience: • 1-4+ years of experience in pharmaceutical regulatory affairs • Preferable exposure to export regulatory submissions and international markets Skills: • Strong knowledge of global regulatory frameworks and export documentation requirements • Hands-on experience with CTD/eCTD dossier preparation and submission tracking • Familiarity with electronic submission systems and regulatory agency portals • Excellent communication, coordination, and stakeholder management skills • Strong organizational ability and attention to detail • Good command of written and spoken English About the Company: The organization operates within the pharmaceutical sector, supporting global product registrations and export compliance across multiple international markets. It emphasizes regulatory excellence, cross-functional collaboration, and adherence to global quality and compliance standards to ensure timely product approvals and sustainable business growth.
Role & Responsibilities: • Assist Clinical Project Managers with day-to-day project administration including preparation of project documents, review of presentations, and participation in internal and client meetings and calls • Act as a liaison between cross-functional teams to ensure timely completion of study milestones and deliverables • Support project start-up, execution, and close-out activities, including finance-related tasks such as invoice reconciliation, budget tracking, and forecasting support • Monitor project progress, track outstanding action items, and respond to internal and client inquiries • Communicate project updates to stakeholders and support issue resolution to maintain project timelines • Serve as acting Project Manager when required under supervision • Verify imaging protocol requirements and ensure queries are reviewed, addressed, and resolved appropriately • Support logistics coordination including materials distribution and tracking • Ensure compliance with SOPs, GCP, ICH, FDA regulations, and quality standards • Contribute to process improvement initiatives and maintain project documentation accuracy • Participate in trainings, team meetings, and perform additional duties as assigned Qualification: • Associate’s degree from a recognized institution • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or related field- preferred Experience: • Minimum 1 year of experience in pharmaceutical drug development, clinical trials, clinical research, or clinical imaging studies • Experience supporting project management activities in a clinical research environment is an advantage Skills: • Strong working knowledge of Microsoft Office tools • Understanding of clinical research, healthcare, or medical imaging processes • Experience with imaging protocols, data verification, and query resolution is desirable • Excellent organizational, interpersonal, and communication skills • Strong attention to detail with the ability to manage multiple tasks • Ability to work independently as well as collaboratively in a team environment • Adaptable, proactive, goal-oriented, and responsive to changing priorities • Professional and positive attitude in all interactions About the Company: Clario is a global leader in medical imaging and clinical trial endpoint technologies with over 30 years of expertise in delivering secure, compliant, and innovative solutions that enhance clinical research. The company partners with pharmaceutical and biotechnology organizations worldwide to unlock better evidence and accelerate the development of life-changing therapies, empowering teams to make a meaningful impact on patient lives every day.
Role & Responsibilities: • Perform triage and initial validity assessment of cases including spontaneous, health authority, clinical trial, and literature cases • Enter and process safety data in pharmacovigilance databases • Conduct initial ICSR assessment, where applicable • Evaluate the need for expedited reporting to health authorities and client partners, ensuring adherence to reporting timelines • Prepare standard safety reporting forms such as CIOMS I, MedWatch forms, and XML files • Prepare and send follow-up requests to obtain missing or additional case information • Submit ICSRs to health authorities and client partners • Complete case documentation in line with project and regulatory requirements • Conduct quality checks on ICSRs to ensure accuracy, completeness, and compliance with industry standards • Perform ICSR search and retrieval from EVWEB database and conduct company vs non-company case assessment • Manage case allocation and workload to meet productivity and quality targets • Provide system and process training to team members • Mentor and support new joiners by guiding them on company processes and fostering a collaborative learning environment • Perform additional responsibilities as assigned by the supervisor in line with process requirements Qualification: • Degree in Pharmacy, Life Sciences, Medicine, or related field Experience: • Relevant experience in Pharmacovigilance / Drug Safety preferred Skills: • ICSR Processing & Case Management • Pharmacovigilance Databases (e.g., EVWEB or similar) • Regulatory Reporting & Compliance • Quality Review & Documentation • Attention to Detail & Analytical Skills • Communication & Team Collaboration About the Company: • Cencora is a global healthcare solutions organization committed to creating healthier futures by improving access to medicines, enhancing patient safety, and supporting pharmaceutical innovation worldwide.