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Role & Responsibilities Perform medical review and analysis of adverse event and adverse reaction reports Conduct signal detection, evaluation and ongoing safety surveillance Provide medical guidance to Drug Safety Associates and Specialists Review narratives for Clinical Study Reports and regulatory documents Prepare and review Benefit Risk Assessments, Safety Evaluation Reports, Clinical Overviews and Expert Statements Act as pharmacovigilance representative and safety scientist Maintain thorough knowledge of assigned product safety profiles Ensure compliance with global regulatory reporting timelines Communicate review issues with Project Managers and stakeholders Perform case medical review, causality assessment, seriousness and expectedness evaluation Conduct medical literature review for safety assessments Qualification Graduation / Post Graduation in Medicine (MBBS / MD) Experience Freshers or candidates with Pharmacovigilance / Drug Safety experience preferred Skills Strong knowledge of GCP, GVP and international PV regulations Excellent written and verbal communication skills Clinical data interpretation and medical judgment Case processing guidance and regulatory compliance Literature review and safety signal analysis Team collaboration and multitasking abilities About the Company A global pharmacovigilance and regulatory services organisation supporting multinational pharmaceutical clients in ensuring patient safety, compliance and lifecycle drug risk management
Role & Responsibilities Review and assess individual case safety reports from clinical trials, spontaneous and solicited sources Determine regulatory reportability and perform case triage Assess seriousness, causality and relatedness of adverse events Review narratives, MedDRA coding, labeling and adverse event selection Escalate complex safety cases to client medical review teams Assess litigation and special case scenarios Coordinate with client therapeutic teams for case resolution Maintain up-to-date product safety profile knowledge Ensure compliance with global health authority regulations Perform additional drug safety activities as assigned Qualification MBBS / MD MCI / State Medical Council Registration Mandatory Experience 1 – 3 years in Pharmacovigilance as Medical Reviewer Skills Safety database handling and MedDRA coding Case triage and regulatory compliance Customer and stakeholder communication Presentation and people management skills Strong organizational, leadership and time management abilities About the Company A leading pharmacovigilance and drug safety services organization supporting global pharmaceutical clients in ensuring patient safety and regulatory compliance
Role & Responsibilities Ensure high quality and regulatory-compliant case processing by vendors Perform quality review of ICSRs and device event reports Review and update vendor SOPs and working procedures Monitor weekly and monthly quality data and identify training needs Review AE/SAE and device event reports for pre and post-marketed products Clarify medical issues, revise MedDRA coding and ensure accurate narratives Coordinate with vendors and internal medical teams for case resolution Support audits, inspections, CAPA documentation and vendor oversight Maintain vigilance documentation and archival processes Train and guide vendor vigilance staff Implement process improvements and corrective actions Qualification BS / MS / Doctorate in Pharmacy, Nursing or related healthcare discipline Experience Minimum 3 years in Pharmacovigilance or Materiovigilance Prior experience in ICSR or device event review preferred Skills Strong knowledge of global PV & MV regulations Experience with safety databases (LSMV, CATSWeb preferred) Excellent communication and interpersonal skills High attention to detail and strong organizational skills Ability to work cross-functionally and manage workflow priorities About the Company A global healthcare organization operating within Global Pharmacovigilance & Risk Management, focused on regulatory-compliant safety surveillance, risk management and medical device vigilance across international markets
Role & Responsibilities Achieve monthly, quarterly and annual clinical and sales support targets Partner with sales teams to provide intensive clinical support to dental professionals Assist dentists with case assessment, ClinCheck usage, record taking and aligner troubleshooting Review ClinChecks for newly trained and existing doctors Transfer complex cases to senior clinical consultants Prepare and provide clinical materials and documentation to customers Deliver clinical training and field coaching to internal teams, distributors and external customers Provide weekly and monthly clinical feedback reports to Clinical Support Manager – India Coordinate mentorship, smile programs and other clinical marketing initiatives Monitor competitor activities and share market intelligence with marketing team Maintain professional conduct, ethical relationships and quality compliance Plan, organize and manage clinical events and speaker programs Build and develop relationships with certified and non-certified Invisalign providers Support new product launches and continuous staff education Manage quality updates and customer product feedback Open to extensive travel Qualification BDS / DDS (Doctor of Dental Surgery) Experience Minimum 2+ years corporate working experience Prior experience in training dentists / orthodontists preferred Skills Strong clinical orthodontic knowledge Excellent communication and presentation skills Proficiency in English Relationship building and training abilities Organizational, reporting and analytical skills About the Company Align Technology is a global leader in clear aligner and digital orthodontic solutions, best known for Invisalign. The organization focuses on innovation, digital dentistry and clinical education while supporting dental professionals worldwide.
Role & Responsibilities Provide general medical consultations via phone and video Diagnose, treat and manage a wide range of primary healthcare conditions Prescribe medications and provide referrals as required Maintain accurate electronic medical records Deliver patient-centred, confidential and ethical telehealth care Manage follow-ups and continuity of care remotely Collaborate with multidisciplinary healthcare teams Qualification MBBS or equivalent Registration with Australian Medical Board (AHPRA) VR and Non-VR GPs eligible Valid visa or Australian citizenship Experience Relevant general practice experience preferred Skills Excellent clinical decision-making skills Strong communication and tele-consultation skills Ability to work independently in a remote setup Time management and organisational skills Professionalism, adaptability and patient-focused care About the Company National Telemedicine Doctors is a fast-growing Australian telehealth medical practice providing accessible, high-quality healthcare services via phone and video across major cities, regional and remote Australia, supported by a strong multidisciplinary and administrative team
Role & Responsibilities Provide dental diagnosis and treatment to patients, perform preventive and restorative dental procedures, maintain patient records, promote oral health awareness, and follow DHS clinical protocols Qualification Bachelor of Dental Surgery (BDS) Experience Freshers and experienced candidates may apply Skills Clinical dentistry procedures, patient handling, communication skills, record maintenance, adherence to government health protocols About the Organisation District Health Society Coimbatore functions under the Tamil Nadu State Health Department and is responsible for delivering primary and public healthcare services across the district, focusing on community-oriented and affordable healthcare deliveryLast Date of Application19-01-2026Application formClick HereOfficial NotificationClick Here
About Role & Responsibilities • Lead clinical education and advocacy initiatives, developing and delivering clinical education programs for patients, clinicians, and diabetes societies • Promote emerging clinical trial data, expanded indications, and strategic publications through presentations and forums • Collaborate closely with cross-functional teams such as Medical Affairs, Marketing, R&D, and Regulatory to meet customer needs and drive product knowledge • Act as a regional expert and serve as a speaker at local, regional, and international congresses • Develop KOLs and drive initiatives to advance Continuous Glucose Monitoring (CGM) as the standard of care in India • Support distributor partners with clinical education and product training to ensure successful product adoption and performance • Design and execute tailored training plans for regional projects and product launches • Leverage Learning Management Systems (LMS) for ongoing learning initiatives and resource development • Provide coaching and feedback to distributor partners, enhancing sales effectiveness and market penetration Qualification • Licensed Medical Doctor (MD), Dietitian (RD/LD), Registered Nurse (RN), or relevant clinical degree required • MD with specialist diabetes experience or Certified Diabetes Educator preferred • Minimum 4 years of experience in diabetes education and treatment, with at least 2 years focused on CGM Experience • Bachelor’s degree with 10+ years of clinical experience or a graduate degree with 6+ years of relevant experience • Proven success in sales training and program design, ideally within healthcare or medical device sectors • Previous experience in diabetes-related medical device sales with a track record of success • Experience in regional strategy or partnership initiatives preferred Skills • Technical knowledge in diabetes technologies, including CGM, and emerging diabetes therapeutics • Strong verbal and written communication skills in English; additional language proficiency in Southeast Asian markets is a plus • Highly organized with excellent project management, problem-solving, and interpersonal skills • Skilled in virtual and in-person training facilitation with proficiency in training delivery tools • Ability to work independently, exercising sound judgment and innovative thinking About the Company Dexcom is a global leader in continuous glucose monitoring (CGM), pioneering the industry for over 25 years. With a mission to empower individuals with personalized, actionable insights to manage diabetes and other health challenges, Dexcom is expanding its focus beyond diabetes to other important health areas.
About Role & Responsibilities • Provide high-quality medical care to a loyal and growing patient base • Practice medicine in a collaborative, supportive, and corporate-free environment • Offer private billing with strong financial performance and high-value consult fees • Maintain high standards of patient care and clinical practice, focusing on quality outcomes Qualification • Registration with AHPRA • FRACGP/FACRRM Registered • Eligible for a Medicare Provider Number • Full working rights in Australia Skills • Excellent clinical skills and the ability to deliver compassionate healthcare • Strong communication and interpersonal skills to build patient relationships • Ability to work in a collaborative, supportive team environment • Passionate about practicing medicine without corporate pressure About the Company This long-established and privately owned medical centre has been delivering exceptional healthcare to the Burleigh Heads community since 1988. With a loyal patient base, AGPAL accreditation, and a focus on quality, the clinic offers a warm, friendly, and collaborative team culture. Located in one of the most desirable beachside suburbs on the Gold Coast, the clinic provides the perfect work-life balance.
About Role & Responsibilities • Lead economic modelling initiatives for health economics and outcomes research (HEOR) • Design and implement economic models for cost-effectiveness and budget impact analysis • Present findings to internal and external stakeholders Qualification • Experience in HEOR (Economic Modeling) Experience • 5+ years of experience in economic modelling and health economics Skills • Proficiency in health economics and statistical modeling tools • Strong communication and presentation skills About the Company Novartis is a global healthcare company dedicated to improving the health and well-being of patients worldwide
About Role & Responsibilities • Conduct health economics and outcomes research (HEOR) in the field of ophthalmology • Perform data analysis, including statistical modeling and cost-effectiveness analysis • Communicate results to stakeholders and support decision-making processes Qualification • Master’s degree or higher in Epidemiology, Biostatistics, Health Economics, Public Health, or related field Experience • 2+ years of experience in HEOR or related data analysis Skills • Strong background in data analysis and statistical techniques • Proficiency in programming languages such as SAS, R, or Python About the Company Alcon Laboratories is a global leader in eye care, providing innovative products and services to improve vision
About Role & Responsibilities • Assist with evidence synthesis and health economics-related tasks • Conduct data analysis and report preparation for clinical studies • Work with cross-functional teams to support decision-making Qualification • M.Pharm, M.Sc, or related discipline / MBBS, MD Experience • 0-2 years of experience in evidence synthesis or related roles Skills • Strong analytical and data interpretation skills • Proficiency in health economics methodologies About the Company Sanofi is a global healthcare leader providing innovative treatments in various therapeutic areas
About Role & Responsibilities • Perform pharmacovigilance activities such as signal detection and risk management • Ensure compliance with regulatory requirements for drug safety • Assist in preparing safety reports and presenting findings Qualification • B.Pharm Experience • 0-2 years in pharmacovigilance Skills • Strong understanding of pharmacovigilance processes • Good communication and report writing skills About the Company Cosette Pharma specializes in the development and commercialization of pharmaceutical products
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
World-class hospital seeking Board Certified Consultant Cardiologists. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
World-class hospital seeking Board Certified Consultant Cardiologists. **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.
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **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.
Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD. **What you will do:** - Lead daily clinical operations. - Mentor junior staff members. - Participate in quality improvement initiatives. **Requirements:** - Proven experience in the field. - Strong communication skills. - Valid license and registration.
About role & responsibilities • Provide clinical dental and allied healthcare services • Diagnose and treat patients as per assigned healthcare role • Support public health programs and community healthcare initiatives • Maintain patient records and treatment documentation • Ensure compliance with healthcare safety and infection control guidelines • Participate in preventive and promotive health activitiesName of the PostsNo.of VacanciesQualificationDental Surgeon01BDS Skills • Clinical assessment and patient management • Communication and record maintenance • Knowledge of public health practices • Team coordination and service delivery Experience • As per post requirement (freshers and experienced candidates can apply) Salary • ₹60,000 per month Benefits • Government healthcare employment • Stable job profile • Fixed monthly salary • No application fee Apply • Submit the filled application to the address mentioned in the notification • Last date to apply: 19-01-2026 About the company • District Health Society Coimbatore is a government public health organization • Provides healthcare services and implements national health programsApplication formClick HereOfficial NotificationClick Here
About role & responsibilities • Perform advanced medical coding of diagnoses, procedures and medications • Code clinical trial data using MedDRA and WHO Drug dictionaries • Ensure accuracy, consistency and regulatory compliance across studies • Resolve complex coding discrepancies and medical queries • Collaborate with clinical, safety and data management teams • Support development and refinement of medical coding SOPs and conventions • Stay updated with global medical coding standards Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Healthcare or related field Skills • Strong working knowledge of MedDRA and WHO Drug • Understanding of clinical trial processes and regulatory requirements • High attention to detail and analytical problem-solving skills • Ability to work in cross-functional global teams • Good documentation and communication skills Experience • Proven experience in medical coding within clinical research Salary • ₹6,00,000 – ₹10,00,000 per annum (estimated) Benefits • Comprehensive health insurance for employee and family • Competitive leave entitlements • Retirement and long-term savings plans • Employee Assistance Programme (24/7 wellbeing support) • Life insurance coverage • Flexible benefits – childcare support, gym discounts, travel subsidies and health assessments • Hybrid / office-with-flex work model About the company • ICON plc is a global leader in healthcare intelligence and clinical research • Provides global clinical trial, regulatory and medical coding solutions
About role & responsibilities • Perform triage and initial validity assessment of adverse event cases • Process spontaneous, clinical trial, literature and authority safety reports • Enter safety data accurately into pharmacovigilance databases • Conduct initial ICSR assessments as per global regulatory requirements • Evaluate cases for expedited reporting timelines • Prepare and submit CIOMS I, MedWatch and XML safety reports • Draft and manage follow-up queries to collect missing information • Maintain audit-ready case documentation • Retrieve and review EVWEB company and non-company cases • Support additional pharmacovigilance activities as assigned Qualification • B.Pharm • M.Pharm • BDS • Life Science Graduate Skills • Strong written and verbal communication • High attention to detail • Basic understanding of pharmacovigilance and drug safety reporting • Ability to work within strict regulatory timelines • Willingness to learn global PV regulations Experience • Freshers and early-career professionals can apply Salary • ₹3,00,000 – ₹5,00,000 per annum (estimated) Benefits • Comprehensive training in global pharmacovigilance operations • Exposure to international regulatory standards and safety systems • Career growth within Cencora / PharmaLex • Inclusive and equal-opportunity work culture About the company • Cencora (PharmaLex India Private Limited) is a global healthcare services organization • Focused on pharmacovigilance, regulatory compliance and risk management • Committed to patient safety, diversity and inclusive workplace practices