Doctor Jobs

Role & Responsibilities Medical review of ICSRs (investigational and marketed products) Perform seriousness, causality and consistency assessments of AEs Ensure compliance with global PV regulations and internal SOPs Collaborate with global safety teams and client medical counterparts Support signal detection and benefit–risk activities Mentor and train case processing and safety teamsQualification MBBS / MD (Mandatory) Knowledge of MedDRA and safety databases (Argus preferred)Experience Minimum 1 year pharmacovigilance experience Minimum 1 year clinical experienceSkills ICSR medical review and AE evaluation Regulatory and SOP compliance MedDRA terminology Argus safety database Strong analytical and communication skills Team mentoring and collaborationAbout the Company Syneos Health is a global biopharmaceutical solutions company delivering integrated clinical and commercial services to improve patient outcomes worldwide.

Role & Responsibilities Provide comprehensive primary medical care to patients across all age groups Diagnose, treat and manage acute and chronic medical conditions Conduct preventative health assessments, health checks and care plans Perform minor procedures, wound care, immunisations and clinical reviews Deliver skin cancer screening and excisions using Fotofinder technology Perform iron infusions and micro ear suction procedures Maintain accurate clinical records and documentation Work collaboratively with on-site pathology, psychiatry and dietitian services Ensure compliance with AHPRA, RACGP and professional clinical standards Provide high-quality, patient-centred care while maintaining continuity of careQualification Fellowship of the Royal Australian College of General Practitioners (FRACGP) Current AHPRA registration Australian Permanent Residency or Australian Citizenship (Mandatory) Eligible to work in MM1 (Not under moratorium)Experience New Fellows are welcome to apply Previous experience in Australian general practice is preferred Experience in skin cancer medicine, chronic disease management, iron infusions or procedural GP work will be an advantageAbout the Company We are a long-established, family-owned mixed billing medical practice serving the community since the mid-1980s. Our clinic is supported by nine experienced General Practitioners, highly skilled Registered Nurses, and a dedicated administrative team with an average tenure of over 10 years.

Role & Responsibilities Provide comprehensive primary healthcare services to registered patients Diagnose, treat and manage acute and chronic medical conditions Perform women’s health, skin health and procedural services as per interest Maintain accurate clinical documentation using Lyrebird AI Scribe Provide preventive care, health education and wellness counselling Utilise fully equipped treatment rooms including ABI machines Participate in bulk billing and private billing services as applicable Work collaboratively with nurses, allied health professionals and support staff Maintain compliance with RACGP, Medicare and Australian healthcare regulationsQualification MBBS or equivalent medical degree Fellowship of RACGP/ACRRM (VR GP) Full AHPRA registrationExperience Experienced VR General Practitioner Open to full-time, part-time or locum engagementSkills Strong diagnostic and clinical decision-making ability Excellent patient communication and consultation skills Ability to work independently and within multidisciplinary teams Interest in women’s health, skin or procedural practice preferredAbout the Company Toowong GP Super Clinic and Montague Road 7 Day Medical Centre are leading primary healthcare centres located minutes from Brisbane CBD. With over 45,000 registered patients, both clinics provide high-quality, patient-focused medical services using modern digital healthcare tools and advanced treatment facilities, offering an ideal environment for GPs seeking excellent income potential with strong work-life balance

Role & Responsibilities • Provide comprehensive outpatient and inpatient medical care • Conduct patient examinations, diagnosis and treatment planning • Prescribe medications and monitor patient progress • Manage emergency and acute medical conditions • Maintain accurate medical records and documentation • Ensure implementation of national health program protocols • Participate in public health initiatives and community outreach programs • Ensure compliance with clinical guidelines and hospital SOPs • Coordinate with nursing staff, specialists and allied healthcare teamsName of the PostsNo.of VacanciesQualificationMedical Officer 07 MBBS, MD/ MS Experience • As per NHM norms Skills • Strong clinical knowledge and diagnostic skills • Good communication and patient counseling skills • Ability to handle emergency medical situations • Knowledge of public health programs and government healthcare policies • Documentation and reporting skills About the Organization The National Health Mission (NHM) Chandigarh works towards strengthening public healthcare services, implementing national health programs, and ensuring accessible, affordable, and quality healthcare for all citizens.Date of Walk-In15-01-2026Application formClick HereOfficial NotificationClick Here

Role & Responsibilities • Identify, segment and engage Key Opinion Leaders (KOLs) and build strong medical expert networks • Develop and execute regional KOL engagement strategies • Deliver non-promotional, scientific exchange and medical education activities • Represent the organization at congresses, advisory boards and medical meetings • Deliver scientific presentations and support content development • Support identification of clinical trial sites and patient recruitment for Phase I–III studies • Facilitate Investigator Sponsored Studies (ISS) • Collaborate with clinical development and operations teams to enhance trial execution • Provide medical and scientific training to internal teams • Respond to unsolicited medical and scientific queries • Review promotional and non-promotional materials for scientific accuracy • Provide medical insights to support brand and business strategy • Develop scientific publications, white papers and medical literature • Ensure compliance with SOPs, medical governance policies and regulatory guidelines • Complete mandatory medical training and certifications Qualification • MBBS or MD (Pharmacology) Experience • 1–2 years pharmaceutical / healthcare / research experience (Oncology preferred) • MD (Pharmacology) freshers can be considered Skills • Strong scientific knowledge of oncology and breast cancer therapies • Excellent communication and scientific presentation skills • Proven KOL engagement and stakeholder management abilities • Strong analytical, planning and decision-making skills • Ability to work cross-functionally and independently About the Company The organization is a leading oncology-focused pharmaceutical company committed to advancing cancer care through innovation, clinical research, and scientific excellence.

Role & Responsibilities • Execute medical affairs strategy in the assigned territory • Understand treatment practices, medicines, and therapeutic trends through KOL interactions, journals, and scientific symposia • Gather, analyze, and disseminate scientific information to internal and external stakeholders • Execute medical projects including IIS studies and key scientific initiatives • Support implementation of medico-marketing strategies • Identify and develop relationships with Key Opinion Leaders (KOLs) and External Experts (EEs) • Provide medical and scientific expertise for new product / indication registrations • Support regulatory defense of marketed products with scientific rationale and literature • Prepare, review, and revise labeling documents as per SOPs • Liaise with regulatory affairs teams and support EE access • Provide regular feedback to management on KOL development and field insights Qualification • Medical degree (MBBS / MD – Pharmacology preferred) • Life Sciences qualification (for experienced field professionals) Experience • 0–3 years of Medical Affairs / Pharmaceutical / Healthcare industry experience • Professionals without doctoral qualification require 10+ years of relevant field experience Skills • Strong scientific expertise in Diabetes therapeutic area • Excellent interpersonal and communication skills • Good presentation and scientific detailing skills • Basic IT knowledge (MS Office) • Ability to work independently in field-based roles About the Company Boehringer Ingelheim is a global biopharmaceutical company operating in human and animal health, focused on developing innovative therapies to improve and extend lives. With a legacy of research excellence since 1885, the company serves over 130 markets worldwide and is one of the largest investors in pharmaceutical R&D.

Role & Responsibilities • Manage and lead a team of Medical Reviewers • Allocate work, monitor productivity and review assignments • Perform quality review of medical record summaries in client-specific formats • Train and onboard new team members • Handle client communication via email and coordination calls • Ensure timely and accurate delivery of assigned projects • Plan and support cross-training initiatives • Maintain compliance with internal quality and documentation standards Qualification • MBBS • MD / MS / Doctorate in any specialization Experience • 5 – 10 years of relevant medical review / healthcare documentation experience Skills • Team management and leadership • Medical record summarization and quality review • Client communication and coordination • Training and mentoring • Strong documentation and analytical skills About the Company The organization provides specialized medical review and clinical documentation services supporting global healthcare and life sciences clients with high-quality medical data review and compliance solutions.

Role & Responsibilities • Provide inpatient and outpatient medical care under assigned departments • Assist consultants in diagnosis, treatment and procedures • Conduct ward rounds and patient monitoring • Maintain clinical documentation and medical records • Participate in emergency and on-call duties • Support teaching and training of interns and junior doctors • Ensure adherence to hospital clinical protocols and standards • Participate in audits, research and academic activitiesName of the PostsVacanciesEducationSenior Resident103Post-graduation,  DNB, MD, MS Experience • As per AIIMS Senior Resident norms Skills • Clinical assessment and patient management • Emergency handling skills • Documentation and reporting • Communication and teamwork • Time and shift management About the Company All India Institute of Medical Sciences (AIIMS), Raebareli is a premier government medical institute delivering advanced healthcare services, medical education and clinical research in Uttar Pradesh.Starting date05-01-2026Closing date20-02-2026 Official Notification and Application FormClick Here

Role & Responsibilities • Provide clinical care in OPD, IPD and emergency services • Assist consultants in patient management and procedures • Perform diagnostic evaluation and treatment planning • Participate in ward rounds and clinical documentation • Support academic and research activities • Ensure adherence to ESIC clinical protocols • Maintain ethical and professional standards of medical practice Qualification • MBBS with Post-graduation / DNB / MD / MS / MDS Experience • As per ESIC Senior Resident norms Skills • Clinical decision-making • Patient management • Medical documentation • Team coordination • Communication skills About the Company Employees’ State Insurance Corporation (ESIC) is a statutory body under the Ministry of Labour & Employment, Government of India, providing comprehensive healthcare and social security benefits to insured workers and their families.Official NotificationClick Here

Role & Responsibilities • Provide specialized clinical care in assigned departments • Assist consultants in OPD, IPD and emergency services • Perform diagnostic evaluation and treatment planning • Participate in ward rounds, clinical documentation and patient follow-up • Support teaching and academic activities • Ensure compliance with hospital clinical protocols • Participate in research and institutional medical programs • Maintain ethical and professional standards of medical practiceName of the PostsNo.of VacanciesQualificationSenior Resident 41MD, MS , DNB, Ph.D, M.Sc Qualification • MD / MS / DNB / Ph.D / M.Sc (as per department requirement) Experience • As per AIIMS Senior Resident norms Skills • Strong clinical judgment • Patient care and case management • Clinical documentation • Team coordination • Communication and interpersonal skills About the Company All India Institute of Medical Sciences (AIIMS) Rajkot is a premier government medical institution dedicated to providing high-quality healthcare, advanced medical education, and research excellence to strengthen India’s public health system.Last Date of Application12-01-2026Official Notification and Apply Online linkClick Here

Role & Responsibilities • Provide OPD and IPD patient care services • Perform clinical examinations, diagnosis and treatment planning • Manage emergency and inpatient medical cases • Maintain accurate patient medical records • Ensure adherence to clinical protocols and hospital policies • Prescribe medications and monitor patient progress • Coordinate with nursing and diagnostic teams • Participate in public health programs and health awareness initiatives • Maintain ethical and professional medical practice standardsName of the PostsVacanciesEducationMedical Officer13MBBS Experience • Freshers and experienced candidates can apply Skills • Clinical diagnosis and treatment • Patient care and counselling • Emergency handling • Medical documentation • Communication and interpersonal skills About the Company Zilla Swasthya Samiti (ZSS), Keonjhar operates under the National Health Mission (NHM) to strengthen public healthcare delivery, improve medical access, and enhance health services across Odisha through government healthcare facilities.Starting date06-01-2026Closing date16-01-2026Official Notification and Application FormClick Here

Role & Responsibilities • Provide comprehensive medical care and treatment to patients • Conduct clinical examinations and diagnose medical conditions • Prescribe medications and treatment plans as per standard guidelines • Monitor patient progress and provide follow-up care • Maintain accurate patient medical records and reports • Ensure compliance with government health protocols and policies • Participate in public health programs and medical camps • Handle medical emergencies and referralsName of the PostsVacanciesEducationMedical Officer480MBBS Experience • Freshers & experienced candidates can apply Skills • Clinical diagnosis and patient management • Medical documentation • Emergency handling skills • Good communication and counselling skills • Basic computer knowledge About the Company Jammu & Kashmir Public Service Commission (JKPSC) is a constitutional body responsible for recruitment to civil services and government medical posts in Jammu & Kashmir, ensuring quality healthcare delivery through public service recruitment.Starting date05-01-2026Closing date04-02-2026Official NotificationClick Here

Role & Responsibilities • Build and maintain scientific relationships with Key Opinion Leaders (KOLs), physicians and       healthcare professionals • Provide accurate, balanced and up-to-date scientific information on company products and    disease areas • Execute Medical Affairs plans for assigned therapeutic areas • Conduct scientific discussions, CMEs, advisory boards and medical education programs • Support clinical research activities and investigator-initiated studies • Collect and communicate field medical insights to internal teams • Support development and review of scientific and medical communication materials • Ensure compliance with regulatory, ethical and company policies during all field       activities • Represent Medical Affairs in internal cross-functional meetings Qualification • MBBS / MD / M.Pharm / PharmD / PhD in Life Sciences or related discipline Experience • 1–3 years of experience in Medical Affairs / Clinical Research / MSL role preferred Skills • Strong scientific and therapeutic area knowledge • Excellent presentation, communication and interpersonal skills • Ability to work independently in a field-based role • Good understanding of clinical research and regulatory guidelines • Willingness to travel within assigned territory About the Company • A leading pharmaceutical organization committed to developing innovative medicines and improving patient outcomes • Focused on delivering high-quality, patient-centric healthcare solutions across therapeutic areas

Role & ResponsibilitiesBuild and maintain strong scientific relationships with Key Opinion Leaders (KOLs), physicians and healthcare professionalsProvide accurate, balanced and up-to-date scientific information on Eisai products and disease areasExecute Medical Affairs plan for assigned therapeutic areasConduct scientific discussions, CMEs, advisory boards and medical education programsSupport clinical research activities and facilitate investigator-initiated studiesCollect and communicate medical insights from the field to internal teamsSupport development and review of medical and scientific communication materialsEnsure compliance with regulatory, ethical and company policies during field activitiesRepresent Medical Affairs in internal cross-functional meetingsQualificationMBBS / MD / M.Pharm / PharmD / PhD in Life Sciences or related fieldExperience1–3 years of experience in Medical Affairs / Clinical Research / MSL role preferredSkillsStrong scientific knowledge and presentation skillsExcellent verbal and written communication skillsAbility to build and manage professional relationshipsGood understanding of clinical research and regulatory guidelinesWillingness to travel and work in a field-based roleAbout the CompanyEisai Pharmaceuticals India is part of Eisai Co., Ltd., a global pharmaceutical company focused on neurology and oncologyEisai is driven by a patient-first philosophy and committed to developing innovative medicines to improve quality of life worldwide

Role & Responsibilities Prepare aggregate safety reports including PBRERs, PSURs, Addendum PSURs, ACOs, PADERs and PSUR line listings Perform quality checks of aggregate safety reports in line with client conventions and regulatory requirements Conduct signal detection activities including cumulative analyses, issue-based event analyses, SERs and Drug Safety Reports Review published literature and case listings for safety surveillance Maintain vigilance over important and designated medical events Interact with client teams to discuss potential safety signals and emerging issues Support preparation and maintenance of Risk Management Plans (RMPs) Perform follow-up with clients to obtain incomplete or missing safety information Perform medical review of Individual Case Safety Reports (ICSRs) Perform medical review of narratives for Clinical Study Reports (CSRs) Provide medical guidance to drug safety scientists on ICSR and CSR narrative processing Maintain up-to-date knowledge of product safety profiles, labeling documents and SOPs Ensure compliance with global regulatory reporting timelines and requirements Maintain accurate safety records in compliance with guidelines and SOPs Qualification MBBS or MD (preferably in a clinical branch) Experience Pharmacovigilance / drug safety experience preferred Skills Strong ability to prepare concise and accurate medical synopses and narratives Ability to evaluate and interpret safety data independently Excellent written and spoken English communication skills Proficiency in MS Word, Excel, PowerPoint and web-based safety applications Strong typing, transcription accuracy and attention to detail About the Company Continuum is a leading contract research organization providing services in Pharmacovigilance, Regulatory, Evidence Evaluation and Technology The organization employs scientists and physicians to support global safety and regulatory operations

Role & Responsibilities Manage processing, follow-up, analysis and regulatory reporting of AEs and SAEs for marketed and investigational human and veterinary products Perform medical evaluation of safety cases in compliance with global regulatory requirements Prepare aggregate safety reports including PBRERs, PSURs, Addendum PSURs, ACOs, PADERs and PSUR line listings Perform quality checks of aggregate safety reports Conduct signal detection related analyses including cumulative and issue-based event analyses Ensure compliance with client conventions, SOPs and global pharmacovigilance guidelines Maintain accuracy, consistency and timelines for all safety deliverables Qualification Master’s degree in Life Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics) BDS / B.V.Sc. / M.V.Sc. Experience Pharmacovigilance industry experience preferred Skills Strong knowledge of medical terminology and pharmacovigilance processes Excellent written and spoken English communication skills Ability to prepare concise and accurate medical synopses and narratives Ability to evaluate safety data independently and draw conclusions Proficiency in MS Word, Excel, PowerPoint and web-based safety applications Strong analytical and documentation skills About the Company Continuum is a leading contract research organization providing services in Pharmacovigilance, Regulatory, Evidence Evaluation and Technology The organization employs scientists and physicians to support global safety and regulatory operations

Role & Responsibilities • Perform initial assessment and medical review of ICSRs in safety databases • Review seriousness, causality, labeling, narratives, MedDRA coding and medical history • Verify suspect drug, concomitant medications and laboratory data • Respond to case owner queries and document medical review comments • Identify and escalate complex case issues to team leads or line managers • Determine follow-up requirements and ensure proper documentation • Train and mentor PV associates on safety conventions and event capturing • Maintain current knowledge of product safety profiles across therapeutic areas Qualification • MBBS / MD (PG degree preferred) Experience • Minimum 8 years of experience in Pharmacovigilance / Drug Safety Skills • Strong knowledge of ICSR medical review • Good understanding of MedDRA coding and global PV regulations • Excellent communication and documentation skills • Strong organizational and mentoring abilities • Ability to work under pressure and meet timelines About the Company • Cencora is a global healthcare solutions organization delivering regulatory, pharmacovigilance and medical safety services through its affiliate PharmaLex India Private Limited, supporting safer medicines and improved patient outcomes worldwide

Role & Responsibilities Perform medical review and assessment of AEs, SAEs and post-marketing ADRs Review narratives, coding, causality, seriousness, expectedness and labeling Prepare and medically review AOSEs, DSUR, PBRER, RMP and ad-hoc regulatory reports Provide medical guidance to PV case processing teams Review safety content of protocols, IBs and CRFs Maintain oversight of product safety profiles across lifecycle Support signal detection and surveillance activities Review and sign off Project Safety Plan and Medical Monitoring Plan Lead training, audits, product transitions and knowledge-sharing initiatives Provide medical escalation and 24-hour safety support as required Represent safety findings in client and internal meetings Maintain compliance with GCP, ICH and global PV regulations Qualification MBBS / MD from a recognized medical institution Valid medical license preferredExperience Minimum 3 years of clinical practice after MBBS/MD Minimum 2 years of pharmacovigilance / pharma / CRO experience preferredSkills Strong knowledge of pharmacovigilance and aggregate reporting Expertise in ICSR medical review and signal detection Good understanding of GCP, ICH and global PV regulations Experience with safety databases (Argus, ARIS-G, LSMV etc.) Excellent communication and documentation skills Strong analytical and leadership abilitiesAbout the Company IQVIA is a leading global provider of clinical research services, healthcare analytics, and commercial insights to the life sciences industry. IQVIA helps accelerate the development and commercialization of innovative medical treatments, enabling better patient outcomes and improved population health worldwide.

Role & Responsibilities • Engage Thought Leaders (Doctors) through scientific exchange, education and data     dissemination • Provide on-label scientific communication and handle unsolicited off-label queries in compliance with regulations • Support and participate in Medical Society interactions and Advisory Boards • Attend congresses and conventions to build relationships and gather competitive intelligence • Plan and conduct scientific training programs and educational events • Identify, profile and segment Thought Leaders and support engagement strategy • Prepare reports and track field activities against objectives • Provide external scientific training and educational support as requiredQualification • MD / MBBS / BAMS / BDS / MDS • Degree in Natural Sciences (Life Sciences / Pharmacy / Biomedical) Required Skills • Knowledge of Women’s Health, Contraception, Endometriosis therapy areas • Understanding of clinical trials and study design • Excellent presentation, communication and scientific writing skills • Ability to work independently and in cross-functional teams • Strong relationship building and stakeholder management skills