Browse the latest opportunities in Doctor Jobs.
Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) from spontaneous and organized data sources • Support review of trial-related adverse events and post-marketing adverse drug reactions • Ensure narrative consistency, seriousness, expectedness, and completeness of clinical information • Support MedDRA coding of adverse events under guidance • Assist with causality assessment and labeling evaluation • Collaborate with senior medical reviewers and team leads to ensure medical accuracy • Participate in quality checks and identify improvements in case documentation • Support audit and inspection readiness through compliant documentation • Contribute to internal trainings, workshops, and knowledge-sharing initiatives • Stay updated on evolving pharmacovigilance regulations and practices Qualification • Medical degree (MBBS or equivalent) • Valid medical license to practice Experience • 1–2 years of clinical experience • Prior exposure to pharmacovigilance or medical review required • Interest in drug safety, clinical data, and regulatory science Skills • Strong medical judgment and attention to clinical detail • Understanding of pharmacovigilance processes and ICSR workflows • Ability to apply MedDRA coding principles • Strong written and verbal communication skills in English • Collaborative mindset with ability to work in global teams • Process-oriented and quality-focused approach About the Company • Teva is a global biopharmaceutical company combining innovative medicines with a strong generics portfolio
Roles & Responsibilities • Support and independently execute research activities under ongoing projects at NABI. • Design, plan, and conduct experiments related to life sciences, biotechnology, or pharmaceutical research. • Analyze experimental data and prepare technical reports, presentations, and documentation. • Maintain laboratory records, project documentation, and ensure data integrity. • Assist in coordination of project activities, timelines, and deliverables. • Ensure compliance with laboratory safety guidelines, SOPs, and institutional policies. • Support procurement, inventory management, and maintenance of laboratory equipment. • Mentor junior research staff and provide technical guidance when required. • Participate in meetings, reviews, and scientific discussions related to project progress. Qualification • MD / MS, M.V.Sc, B.Pharm, MDS (from a recognized university / institution) Experience • Relevant research or project experience in life sciences, biotechnology, pharmaceutical sciences, or allied fields is preferred. • Experience in handling laboratory techniques, data analysis, and research documentation is desirable. Skills • Strong understanding of research methodologies and experimental design. • Good analytical, documentation, and reporting skills. • Ability to work independently and in a multidisciplinary team environment. • Proficiency in MS Office and basic research data tools. • Effective communication and coordination skills. Age Limit • Minimum Age: 21 Years • Maximum Age: 40 Years • Age relaxation as per NABI / Government of India norms. Walk-in Interview Details • Date: 03-02-2026 • Venue: National Agri-Food Biotechnology Institute (NABI), Knowledge City, Sector-81, Mohali, Punjab – 140306 About the Organisation National Agri-Food Biotechnology Institute (NABI) is an autonomous institute under the Department of Biotechnology, Government of India, dedicated to translational research in agri-food biotechnology to improve human nutrition, food security, and agricultural sustainability.Application formClick HereOfficial NotificationClick Here
Role & Responsibilities • Oversee adherence to prescribed dose status across assigned clinical trial sites • Identify prescribed vs expected dose discrepancies and drive traceable follow-ups • Collaborate with Clinical Medical Managers and Medical Advisors on dose-related issues • Document dose-related operational risks and maintain inspection-ready records • Execute routine and ad-hoc dose surveillance reviews as per protocol requirements • Support site engagement through clear communication and timely escalation • Partner with Trial Managers on dose and retention-related matters • Coach site staff on dose compliance, documentation quality, and protocol adherence • Communicate findings to trial squads and medical partners for informed decisions • Contribute to continuous improvement and development of surveillance processes Qualification • Graduate degree in Life Sciences (M.Pharm, PharmD, Pharmacy, BDS/MDS, MSc Nursing) • Strong understanding of clinical trial conduct and ICH-GCP Experience • Minimum 2 years’ experience in clinical trials (pharma/biotech/CRO/hospital) • Strong knowledge of clinical trial data, systems, and global operations • Experience working with cross-functional and global stakeholders Skills • Excellent communication and relationship-building skills • Strong analytical and problem-solving abilities • Familiarity with clinical IT systems and trial tools • Ability to work independently in dynamic environments • High ownership, motivation, and continuous improvement mindset • Ability to coach, influence, and manage stakeholders effectively About the Company • Novo Nordisk is a global healthcare company with over 100 years of innovation , Strong focus on patient safety, clinical quality, and data integrity
Role & Responsibilities • Create and answer complex radiology cases and diagnostic reasoning questions for AI model training • Review AI-generated radiology reports for accuracy, completeness, and clinical relevance • Analyse and rank AI model outputs to identify reasoning gaps, factual errors, or unsafe recommendations • Provide structured expert feedback to improve AI diagnostic logic and imaging interpretation • Contribute to enhancing AI performance in medical imaging and clinical decision support Qualification • Medical degree or currently pursuing (MD, DO, MBBS or equivalent) • Radiology training or experience from an accredited program Experience • Practicing or recently practicing radiologists, fellows, or radiology residents • Experience in clinical imaging interpretation preferred Skills • Strong clinical judgement and diagnostic reasoning skills • Ability to assess scientific rigor and clinical soundness • Excellent written English for technical review and feedback • Attention to detail and structured analytical thinking • Ability to work independently in a remote, project-based environment About the Company • Quik Hire Staffing provides remote and contract-based clinical and technical talent, Supports advanced AI and healthcare research initiatives
Roles & Responsibilities:• Assess patients’ physical health, mobility, and functional limitations• Develop and implement personalized physiotherapy and rehabilitation programs• Provide evidence-based physiotherapy treatments to improve mobility, recovery, and overall physical well-being• Monitor patient progress and adjust treatment plans as required• Educate patients on exercises, posture correction, and injury prevention• Maintain accurate patient records and documentation• Ensure adherence to clinical protocols, safety, and hygiene standardsQualifications:• Bachelor’s (BPT) or Master’s (MPT) degree in PhysiotherapyExperience:• Freshers are welcome to apply• Relevant clinical experience is an advantageSkills Required:• Strong assessment and physiotherapy skills• Good communication and interpersonal abilities• Compassionate, patient-centered, and professional approach• Ability to work independently and as part of a clinical teamAbout the Company:Muskan Physiotherapy Clinic, Bengaluru, is a patient-focused clinic dedicated to improving mobility, recovery, and overall physical well-being. The clinic emphasizes evidence-based physiotherapy care, compassionate service, and flexible scheduling to meet patient needs.
Role & Responsibilities • Provide medical and scientific support across current and upcoming Medical Aesthetics portfolios • Own and drive Key Opinion Leader (KOL) identification, development, and engagement • Lead scientific exchange with HCPs and share insights with cross-functional teams • Advise on brand strategy and contribute to tactical planning with marketing teams • Execute Medical Affairs plans for Saudi Arabia and MEA region • Deliver scientific education and training initiatives across the aesthetics portfolio • Conduct field visits, advisory board meetings, and clinical trial facilitation • Serve as a medical resource for internal and external stakeholders • Support medical-marketing messaging and approval processes • Ensure pharmacovigilance, compliance, and ethical standards are maintained • Contribute to internal training, external education, and thought-leadership initiatives Qualification • Medical degree (MD) or advanced science degree (PhD) preferred • Master’s or Bachelor’s degree in a scientific discipline (including Pharmacy) considered with relevant experience Experience • Minimum 2–5 years’ experience in the pharmaceutical industry • Experience in dermatology, plastic surgery, or medical aesthetics preferred • Medical Affairs experience including advisory boards, publications, and scientific exchange • Proven experience developing and maintaining KOL relationships • Strong understanding of local Saudi market and multinational work culture • Based in Riyadh with willingness to travel as required Skills • Strong scientific communication and presentation skills • Strategic thinking and country-level planning capability • Ability to engage and influence HCPs, KOLs, and internal stakeholders • Leadership and persuasion skills across commercial and medical teams • In-depth understanding of medical aesthetics and clinical concepts • High ethical standards with strong compliance orientation • Fluent English (verbal and written) • Proficiency in MS Office and related tools About the Company • Allergan Aesthetics is part of AbbVie, a global biopharmaceutical leader , Focused on advancing innovation in medical aesthetics.
Role & Responsibilities • Support pre-commercial clinical trials and scientific collaborations focused on retina programs • Act as field-based Medical Affairs representative to build and maintain KOL relationships • Support clinical trial recruitment and site outreach activities • Communicate field insights and feedback to Clinical Operations and Development teams • Conduct scientific exchange to gather insights and inform Medical Affairs strategies • Serve as a medical resource for unsolicited inquiries on investigational products • Develop and support clinical and scientific communications, presentations, and FAQs • Participate in KOL mapping and execution of customer-centric engagement plans • Represent Medical Affairs at medical congresses and scientific meetings • Support patient advocacy initiatives and outreach activities • Travel 50–70% as required for field-based responsibilities Qualification • Master’s degree (MPH or equivalent) required • Doctorate degree (MD, OD, PharmD, PhD) preferred Experience • Minimum 3 years’ experience in ophthalmology, retina diseases, and/or gene therapy • Experience in field-based scientific exchange or clinical trial support • Exposure to Medical Affairs or MSL roles preferred Skills • Strong scientific communication and relationship-building skills • Ability to rapidly assimilate and interpret clinical data • Excellent medical writing and presentation skills • Proactive problem-solving and project management abilities • Ability to work collaboratively across cross-functional teams • High level of organization, flexibility, and resilience • Innovative and strategic mindset aligned with Medical Affairs objectives About the Company • REGENXBIO is a leading biotechnology company focused on AAV gene therapy development , Dedicated to advancing innovative treatments for patients with serious diseases
Role & Responsibilities • Perform quality control (QC) of pharmacovigilance cases • Conduct medical evaluation of adverse event reports • Enter vigilance case data into agreed databases and formats • Perform follow-up of cases via phone and email • Pre-analyse complex cases prior to data entry • Evaluate cases for medical coding as per applicable dictionaries • Assess causality between suspect product and reported events • Determine seriousness and expectedness of events • Identify regulatory submission requirements for each case • Validate documents prepared by Vigilance Associates or Data Managers • Close vigilance case files in compliance with timelines • Support setup and review of ICSR / MLM filters • Analyse inclusion or exclusion of EV / MHRA cases • Provide medical input to the Medical Information division • Support client-specific pharmacovigilance activities within the business unit Qualification • Doctor (MBBS or equivalent) or Pharmacist by training Experience • Minimum 3 years’ experience with service providers in pharmacovigilance • Hands-on experience in QC of safety cases • Experience with SafetyEasy database (mandatory) Skills • Strong knowledge of global pharmacovigilance regulations • Experience working with safety databases • Process-oriented and detail-focused approach • Ability to multitask and manage multiple priorities • Proficiency in Microsoft Office tools • Excellent written and verbal communication skills in English • Strong teamwork and collaboration skills • Flexible and adaptable in a dynamic environment About the Company • ProductLife Group is a global life sciences consulting and services company , Supports pharmaceutical, biotech, and medical device companies across the product lifecycle.
Role & Responsibilities • Provide and supervise comprehensive medical care to people in prison • Deliver, monitor, and evaluate medical programs and healthcare services • Coordinate clinical hours and on-call duties with the Health Services Manager and Director, Medical Services • Work collaboratively within a multidisciplinary healthcare team • Maintain high standards of clinical governance and quality care • Operate effectively within a secure correctional healthcare environment Qualification • Medical Practitioner registered with the Medical Board of Australia (from 1 July 2010) • Documentary evidence of current medical indemnity insurance Experience • Minimum 5 years post-graduate clinical experience • Experience in mental health, drug and alcohol, and emergency care (desirable) • Demonstrated ability to deliver high-quality patient-centred care Skills • Strong written and verbal communication skills • Ability to work effectively within multidisciplinary teams • Sound clinical judgement and professional accountability • Computer literacy relevant to clinical documentation and reporting • Commitment to ongoing professional development About the Company • GEO Healthcare delivers primary and related health services in Victorian men’s public prisons , Subsidiary of The GEO Group Australia Pty Ltd with over 30 years of experience.
Role & Responsibilities • Promote company’s therapy-focused pharmaceutical products to specialist doctors • Develop strong scientific engagement and long-term professional relationships with consultants • Conduct effective product detailing with strong clinical knowledge • Organize CMEs, RTMs, and scientific promotional activities • Achieve therapy-wise prescription generation and sales targets • Monitor competitor brands and market trends in the therapy segment • Ensure product availability at hospitals and key pharmacies • Maintain daily call reports, doctor data, and sales records Qualification • B.Sc (Biology) / B.Pharm Experience • Minimum 1–2 years of pharmaceutical field sales experience • Experience in specialty/therapy segment preferred Skills • Strong therapy and product knowledge • Scientific communication ability • Relationship building with specialist doctors • Target-oriented approach • Good presentation and interpersonal skills About Company Unifaith Biotech Private Limited is a growing pharmaceutical company focused on delivering quality healthcare solutions. The company emphasizes scientific promotion, strong doctor relationships, and expanding its presence in specialized therapy segments.
Roles & Responsibilities:• Deliver comprehensive clinical onboarding, training, and implementation support to dental professionals on SureSmile aligner workflows• Assist clinicians with case selection, treatment planning guidance, and troubleshooting throughout aligner therapy• Conduct chairside and virtual training sessions to ensure smooth adoption of SureSmile in clinical practice• Collaborate with sales and product teams to drive clinical conversions and support practice growth• Build and maintain strong professional relationships with clinicians to ensure satisfaction and protocol adherence• Support and facilitate workshops, webinars, and regional clinical education programsQualifications:• BDS or MDS with specialization or substantial experience in Orthodontics (mandatory)• Strong hands-on knowledge of aligner therapy, digital workflows, and core orthodontic principlesExperience:• Clinical experience in orthodontics and aligner-based treatments preferred• Experience in clinical training, implementation, or education roles is an advantageSkills Required:• Strong understanding of aligner systems and digital orthodontics• Experience with CAD/CAM systems, dental software, or digital dentistry platforms preferred• Excellent communication and presentation skills• Ability to train, educate, and support clinicians effectively• Strong interpersonal and relationship-building abilities• Professional, proactive, and performance-driven approachAbout the Company:Dentsply Sirona is the world’s largest manufacturer of professional dental products and technologies, with over 130 years of innovation. The company develops, manufactures, and markets comprehensive dental and oral healthcare solutions, empowering dental professionals worldwide to deliver safer, more effective, and advanced patient care.
Lead cross-functional medical programs to ensure clinical and scientific support for products. Engage healthcare professionals, support clinical trials, and disseminate medical data. Requires coordination of medical education, compliance, and real-world evidence generation.
About the Role: Johnson & Johnson is seeking an accomplished Associate Director, Global Medical Affairs to lead scientific strategy and medical excellence across its global portfolio. This role is pivotal in shaping evidence generation, scientific communication, and external engagement to advance patient outcomes worldwide. The successful candidate will collaborate closely with cross-functional teams and serve as a scientific leader and strategic partner within the organization. Key Responsibilities: Develop and execute comprehensive global medical affairs strategies for assigned products or therapeutic areas. Lead scientific communication planning, including publications, congresses, and medical education initiatives. Provide medical insights to R&D teams and support global clinical development and evidence-generation activities. Establish and maintain relationships with global Key Opinion Leaders (KOLs) and external scientific experts. Guide real-world evidence (RWE) programs, post-marketing studies, and other data-generation initiatives. Represent medical affairs at advisory boards, congresses, and cross-functional strategic meetings. Ensure adherence to global medical, ethical, and regulatory standards in all medical affairs activities. Qualifications: Advanced degree (MD, PharmD, PhD, or equivalent) is required. 8–12 years of experience in Medical Affairs or related roles in pharmaceutical or biotech industries. Strong expertise in medical strategy, evidence generation, and scientific communications. Proven leadership experience within a global/matrix organizational structure. Excellent communication, stakeholder management, and analytical skills. Why Johnson & Johnson: Opportunity to influence patient outcomes on a global scale. Collaborative and innovative work environment. Professional growth and leadership development opportunities.
About the Role The Medical Affairs Specialist will support Roche’s medical strategy by providing scientific expertise, engaging with healthcare professionals, ensuring compliant dissemination of medical information, and contributing to evidence generation activities. This role plays a key part in aligning medical insights with business objectives and improving patient outcomes across therapeutic areas. Key Responsibilities Scientific & Medical Expertise Provide accurate, balanced, and up-to-date scientific information to internal teams and external stakeholders. Support the development and review of medical/scientific materials, including slide decks, publications, and promotional content. Maintain deep knowledge of assigned therapeutic areas, clinical data, competitors, and market trends. Medical Insights & Stakeholder Engagement Build trusted relationships with Key Opinion Leaders (KOLs), clinicians, and scientific communities. Capture and communicate medical insights to shape Roche’s medical strategies and evidence-generation plans. Support advisory boards, scientific meetings, and investigator-initiated studies. Evidence Generation & Medical Governance Assist in planning and executing local clinical studies, real-world evidence projects, and post-marketing surveillance. Ensure scientific accuracy and compliance with local/global regulatory, legal, and ethical standards. Support pharmacovigilance teams with medical evaluation and safety reporting when required. Cross-Functional Collaboration Partner with commercial, regulatory, market access, and marketing teams to ensure medically sound strategies. Provide medical training to internal teams, including sales and field force, to enhance scientific competency. Contribute to launch readiness, disease education programs, and patient support initiatives. Qualifications & Experience Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine (MBBS/MD preferred). 2–5 years of experience in Medical Affairs, Clinical Research, or related pharmaceutical industry roles. Strong understanding of clinical trials, medical governance, and scientific communication. Excellent communication, analytical, and stakeholder management skills. Ability to work in a fast-paced, matrixed environment and manage multiple priorities. Why Join Roche? Work in a globally respected healthcare company committed to innovation and patient-centricity. Opportunity to collaborate with world-class medical professionals and access cutting-edge scientific resources. Inclusive work environment with strong career development pathways.
Role Overview Responsible for driving medical strategy, providing scientific leadership, and supporting AstraZeneca’s therapeutic areas through evidence-based medical activities, stakeholder engagement, and compliance-driven execution. Key Responsibilities Develop and implement medical plans aligned with global/regional strategies. Serve as scientific expert and deliver accurate, balanced medical information. Engage and build strong relationships with KOLs and external HCPs. Support clinical trials: feasibility, protocol review, and execution. Lead medical reviews of promotional and non-promotional materials. Provide medical training to internal teams and support product launches. Ensure strict compliance with regulatory, ethical, and AstraZeneca governance standards. Skills & Competencies Strong clinical and scientific knowledge. Excellent communication and presentation skills. Ability to interpret scientific data and provide actionable insights. Collaborative mindset with high ethical standards. Qualifications MBBS/MD required. 2–5 years in Medical Affairs or relevant clinical/scientific roles preferred.
Role Overview: Lead Bayer India’s Medical Affairs function, shaping scientific strategy, driving evidence generation, and strengthening external medical engagement across the Pharmaceuticals portfolio. Responsible for medical excellence, compliance, and cross-functional partnership to support patient outcomes and business growth. Key Responsibilities: Develop and execute national Medical Affairs strategy aligned with global/regional plans. Provide scientific leadership for launches, lifecycle management, and evidence-generation (IITs, RWE, Phase IV). Lead KOL engagement, advisory boards, medical education, and scientific communications. Oversee medical review, governance, and regulatory-compliant scientific exchange. Partner with Commercial, Market Access, Regulatory, and PV to shape brand plans and market strategy. Lead, coach, and develop medical managers and MSL teams. Qualifications: MBBS/MD with 12–18+ years of Medical Affairs experience in pharma MNCs. Strong expertise in scientific strategy, clinical research, compliance, and stakeholder management. Proven leadership skills with high scientific, ethical, and strategic acumen.