Doctor Jobs

Role & Responsibilities • Plan and execute field activities to disseminate medical knowledge on Rare Blood Disorders • Provide healthcare professionals with information on relevant clinical studies and treatment guidelines • Organize scientific meetings and lectures with stakeholders • Collaborate with Key Opinion Leaders (KOLs) on diagnostic and management strategies for patients with hemophilia • Gather insights from healthcare professionals and provide actionable feedback to Sanofi • Ensure compliance with ethical standards and regulations in the pharmaceutical market Qualifications • Advanced degree in a technical, scientific, or medical field (MBBS, MD, or equivalent) Experience • 2-4 years of experience in a medical or scientific liaison role, preferably within rare blood disorders Skills • Strong scientific knowledge in Rare Blood Disorders, particularly hemophilia • Proven ability to build relationships with Key Opinion Leaders and healthcare professionals • Experience in organizing and conducting scientific meetings and lectures • Strong communication and presentation skills • Ability to gather and analyze insights to inform business strategy About The Company • Sanofi is a global healthcare and pharmaceutical company specializing in innovative drug development and delivering high-quality medical products.

Role & Responsibilities • Engage healthcare professionals with impactful scientific discussions aligned to the medical strategy • Identify data gaps and opportunities for real-world evidence and precision medicine • Gather field insights to inform product strategy and evidence generation plans • Support clinical trial execution and site education initiatives • Collaborate with cross-functional teams to improve patient access and outcomes • Deliver tailored scientific content through digital and in-person channels Qualifications • Medical degree (MBBS, MD, or equivalent) • Solid understanding of healthcare systems, research procedures, and industry guidelines Experience • Minimum 3 years of experience in a medical function within a therapeutic area • Proven ability to apply digital solutions for stakeholder engagement and field medical insights Skills • Strong communication and presentation skills • Ability to engage healthcare professionals effectively • Knowledge of real-world evidence generation and precision medicine • Experience in clinical trial support and scientific content delivery About The Company • Novartis is a global healthcare company specializing in innovative drug development, patient-centered solutions, and delivering high-quality medical products.

Role & Responsibilities • Implement local medical plans by executing the national Medical Affairs strategy within your region • Establish and maintain scientific relationships with KOLs, diabetes specialists, and other relevant stakeholders to drive scientific exchange and advocacy for Novo Nordisk’s portfolio • Gather and communicate clinical insights by attending scientific meetings and engaging with HCPs to capture clinical needs, trends, and unmet needs • Collaborate with marketing and sales teams to sharpen product positioning and promotional tactics • Develop and deliver scientific training and educational activities for physicians and allied HCPs • Provide medical advice and support to the brand team and other internal stakeholders on clinical data, label information, and therapeutic positioning • Ensure compliance with local regulations, Novo Nordisk policies, and ethical standards for scientific engagement Qualifications • MD, MBBS from a recognized institution • Solid understanding of diabetes, obesity, and related metabolic disorders Experience • Minimum 2 years’ relevant experience in Medical Affairs (Desirable) • Experience in gathering clinical insights and supporting medical education/training activities Skills • Strong knowledge of diabetes, obesity, and related metabolic disorders • Ability to interpret clinical data and treatment paradigms • Excellent communication and relationship-building skills with KOLs and other stakeholders • Ability to collaborate with cross-functional teams in a medical and commercial context • Strong attention to compliance and ethical standards About The Company • Novo Nordisk is a global healthcare company, with a strong focus on diabetes, obesity, and other serious chronic conditions. With decades of experience, Novo Nordisk is dedicated to providing innovative treatments and improving the lives of patients worldwide.

Roles & Responsibilities:• Perform root canal treatments (RCT) and tooth extractions• Conduct scaling and polishing procedures• Provide denture fittings and related treatments• Ensure high standards of patient care, comfort, and safety• Educate patients on oral hygiene and preventive dental care• Maintain accurate patient records and follow clinical protocols• Collaborate with clinic staff to ensure smooth workflow and patient satisfaction• Adapt to flexible working hours as requiredQualification:• Bachelor’s degree in Dental Surgery (BDS) or equivalent dental qualificationExperience:• Relevant clinical experience as a Dental Surgeon preferredSkills:• Endodontics (RCT), extractions, and general dentistry procedures• Denture management and fitting• Patient communication and education skills• Attention to detail and adherence to safety protocols• Teamwork and professional conduct• Flexibility in working hoursAbout the Company:DocHome | Home For Doctors is a Bengaluru-based dental healthcare provider focused on delivering high-quality, patient-centric care. The clinic offers comprehensive dental services, emphasizing modern techniques, professional ethics, and comfort to ensure optimal oral health and patient satisfaction.

Role & Responsibilities Identify, develop, and maintain collaborative relationships with KOLs, scientific experts, and other medical stakeholders. Deliver high-quality medical and scientific communications in line with defined communication plans. Create and execute stakeholder engagement plans, adhering to Sobi’s high standards. Support the country Hemophilia team in developing local medical tactics and provide input to HQ/regional plans if relevant. Organize and set up scientific advisory boards with key stakeholders, in collaboration with HQ. Work with the local patient access team to support local access. Contribute and support medical scientific aspects in various activities locally and regionally. Provide local and regional feedback to Regional office when performing Business Development Due Diligence. Coordinate ISSs and NPU as appropriate. Handle medical information enquiries in collaboration with HQ in Stockholm. Attend relevant local, regional, and global congresses and symposiums to represent Sobi and interact with stakeholders. Represent the scientific interests in internal and external forums and interact with KOLs at hospitals, patient associations, and other NGOs within the therapeutic area. Maintain and develop strong relationships with scientific societies and central decision-makers at local health authorities. Provide advice to the organization and management on medical matters and their legal implications. Ensure that medical and scientific knowledge for the therapeutic area remains at the forefront of contemporary thinking. Report to management in accordance with Sobi requirements and standards. Lead a team of Medical Science Liaisons (MSLs) and provide medical leadership with partners. Qualification Bachelor's degree in a medical field (Pharmacy, Medicine); postgraduate degree preferred. Experience 8+ years of experience in the medical function within the Pharmaceutical Industry. Experience in Haematology & Rare diseases field; GCC markets experience is a plus. Demonstrated ability to manage a diversified portfolio and meet medical KPIs. Skills Fluency in written and spoken English & Arabic. Proficiency in Microsoft Office suite. Strong operational discipline and execution skills. Alignment with Sobi core values: Care, Ownership, Urgency, Partnership, Ambition. About The Company Sobi - Swedish Orphan Biovitrum AB (publ) is a global biopharmaceutical company focused on providing innovative therapies for rare diseases. Sobi’s commitment to science and collaboration enables them to deliver life-changing treatments to patients worldwide. Their culture is driven by a desire to make a positive impact on the world’s most challenging health conditions, with a focus on rare diseases.

Role & Responsibilities • Review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. • Review includes coding, assessment of seriousness, expectedness, and causality. • Write Company comments, follow-up questions, and analyze similar events. • Complete all required supporting documentation, such as trackers. • Support the Qualified Person for Pharmacovigilance (if not medically qualified) in the medical understanding and evaluation of any safety issues. • Review and provide input in periodic reports. • Review literature screening search strategies and review articles to determine if they contain ICSRs/SAEs related to the relevant Medicinal Product or other safety-related findings. Qualification • MD qualification is required. Experience • Proven ability to plan, organize, prioritize, and execute multiple tasks efficiently. Skills • Ability to work cross-culturally and cross-functionally, valuing teamwork. • Strong communication and presentation skills. • Advanced English skills, both verbal and written (at least B2 level). • Advanced knowledge of MS Office. About The Company • PrimeVigilance offers an opportunity for Medical Doctors to develop a career in Drug Safety.The company’s Pharmacovigilance Physician team operates across North America, Europe, and Asia, providing global pharmacovigilance services. PrimeVigilance is focused on creating a collaborative, high-quality environment for physicians interested in pharmacovigilance.

Role & Responsibilities • Author medical writing tasks, including aggregate reports, Risk Management Plans (RMPs), and other documents throughout the product’s life cycle. • Responsible for the quality and content of documents, as well as quality control review of documents prepared by medical writing peers. • Engage in continuous self-education regarding all aspects of medical writing activities. • Actively participate in training sessions, maintenance, and development of quality system documents. • Support pharmacovigilance operations associated with medical writing. Qualification • PhD or MSc in Life Sciences or Healthcare (e.g., pharmacy, biology, chemistry, veterinary medicine). Experience • Previous experience in drug safety medical writing, including PBRERs, DSURs, and RMPs. Skills • Strong time management, organization, and multitasking skills with excellent attention to detail. • Strong communication and presentation skills. • Advanced knowledge of MS Office. • Fluency in English (both verbal and written). About The Company • PrimeVigilance offers an opportunity for medical writers to further develop their careers in pharmacovigilance medical writing.

Role & Responsibilities • Review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports for medical and causality assessments. • Assess the seriousness, expectedness, and causality of reports. • Write company comments, follow-up questions, and perform analysis of similar events. • Complete required supporting documentation such as trackers. • Support the Qualified Person for Pharmacovigilance (QPPV) in evaluating safety issues (if not medically qualified). • Provide input for periodic reports. • Review literature screening search strategies and articles to determine safety findings or ICSRs/SAEs related to the relevant medicinal products. Qualification • MD (Medical Doctor) Experience • Experience in Pharmacovigilance, preferably with exposure to ICSR handling and safety reporting • Strong understanding of drug safety regulations and practices Skills • Ability to plan, organize, prioritize, and execute multiple tasks • Strong communication and presentation skills • Ability to work cross-culturally and functionally as part of a global team • Advanced English skills (both verbal and written), at least B2 level • Advanced knowledge of MS Office About The Company • PrimeVigilance is a global pharmacovigilance and drug safety service provider. The company offers an opportunity for medical doctors to build and develop their careers in drug safety.

Roles & Responsibilities: • Manage end-to-end TMF and document management operations in compliance with ICON SOPs, client requirements, and regulatory guidelines • Lead and mentor 20–30 TMF professionals, ensuring high performance and quality delivery • Coordinate TMF activities across multiple studies and clients • Generate and present TMF status reports for internal stakeholders and clients • Drive process improvement initiatives to enhance efficiency and quality • Ensure TMF inspection readiness and participate in internal and external audits • Oversee TMF archiving activities and study close-out documentation • Liaise with clinical study teams, training departments, and clients • Manage quality control, tracking, and compliance metrics • Support departmental and cross-functional projects as assigned Qualification: • Bachelor’s degree in Science, Medicine, Pharmacy, Life Sciences, or equivalent • Strong understanding of clinical study start-up, maintenance, and close-out activities Experience: • 12+ years of experience in TMF Operations within clinical research or CRO environments • 3+ years of people management experience managing large teams (20–30 members) Skills: • Excellent organizational, communication, and stakeholder management skills • Proven ability to manage multiple projects and global clients • Strong analytical, problem-solving, and conflict management skills • Willingness to travel up to 25% (domestic/international) About the Organisation: ICON plc is a global leader in healthcare intelligence and clinical research, known for its strong culture of Accountability, Collaboration, Partnership, and Integrity. ICON provides professionals the opportunity to work on global clinical trials, shaping the future of drug development while delivering high-quality solutions to clients worldwide.

Roles & Responsibilities: • Collaborate with in-country regulatory representatives to develop strategies and prepare submissions for India and APAC markets • Create, review, and approve product labeling, including Instructions for Use (IFUs), packaging, and other materials for the APAC region • Represent Regulatory Affairs on cross-functional teams, providing strategic input and technical guidance on regional requirements • Offer regulatory guidance to the software development team • Review advertising and promotional materials for compliance with local regulations • Assess the regulatory impact of design and manufacturing changes and execute necessary actions • Monitor new and evolving regulations in APAC countries, evaluating impacts on existing registrations and internal procedures • Provide regulatory support during internal and external audits • Perform other duties as assigned to support team and company goals Qualification: • Bachelor’s degree in a relevant field • Strong knowledge of India and international regulatory requirements for medical devices, including submission processes, labeling, promotion regulations, quality control, and quality management systems • Expertise in Medical Device Software, software development lifecycle, IEC 62304 standards, and software classification Experience: • Minimum 5–8 years of related experience • Prior experience with regulatory submissions in India preferred Skills: • Excellent technical writing, editing, and analytical skills • Strong problem-solving, proactive learning, organizational, and communication skills • Ability to work independently and collaboratively in a cross-functional team environment About the Organisation: Dexcom Corporation is a global leader in continuous glucose monitoring (CGM) technology, revolutionizing diabetes management for millions worldwide. With over 25 years of innovation, Dexcom empowers people to take control of their health through advanced biosensing solutions and is expanding its impact in the APAC region, including India, driving meaningful health outcomes through cutting-edge medical device technology.

Role & Responsibilities • Conduct physical examinations and assess patients' health conditions • Provide comprehensive patient care and ensure patient well-being • Collaborate with specialists for multi-disciplinary care as required • Maintain accurate patient records and document medical findings • Provide consultations and follow-up care to patients • Ensure adherence to hospital policies, medical guidelines, and safety standards Qualification • MBBS degree (required) Experience • Minimum 1 year of experience as a Resident Medical Officer (RMO) • Preferred: Experience as a physician for 1 year Skills • Strong knowledge of physiology and medical principles • Excellent communication skills and patient care abilities • Experience in conducting physical examinations and diagnostic procedures • Ability to work under pressure in a multi-speciality hospital setting About The Company • India Hospital is a multi-speciality hospital providing high-quality healthcare services to the community. The hospital is known for its dedicated healthcare team and commitment to patient care and treatment.

Role & Responsibilities • Talking to real patients every day, understanding their stories, symptoms, and goals • Ordering tests, interpreting blood reports, and building holistic diagnoses • Creating and updating personalized care plans (nutrition, supplementation, sleep, stress, etc.) • Following up with patients continuously, handling flare-ups, doubts, frustrations, and celebrations • Learning and sharpening clinical and communication skills through regular training sessions • Treating patients with autonomy, with the freedom to make calls based on your judgment • Collaborating with health coaches, designers, engineers, writers, and even filmmakers to create a unique healthcare experience Qualification • MBBS degree • Medical Council of India (MCI) registration certificate Experience • 0+ years of experience in clinical practice Skills • Excellent interpersonal skills and communication abilities • Ability to provide patient-centered care • Strong diagnostic and problem-solving skills • Proficiency in interpreting medical data and making informed decisions • Curiosity and a hunger to learn and grow quickly About The Company • Amura Health is a dynamic, science-backed healthcare company based in Chennai, revolutionizing how healthcare is delivered by operating as a "hospital on the cloud.

Roles & Responsibilities • Manage end-to-end scientific writing and publication workflows using Pub Connect. • Create and maintain publication plans, author approvals, versions and checklists. • Coordinate journal and congress submissions including pre-submission inquiries and dummy submissions. • Track submission requirements, guideline updates and provide status updates to stakeholders. • Prepare and collate metadata and complete submission packages. • Ensure accurate documentation from kick-off through review, sign-off and approvals. • Support system activities such as uploads, reference linking and workflow monitoring. • Ensure compliance with journal/congress guidelines, SOPs, client standards and templates. • Perform literature searches and provide ad-hoc operational support as required. • Manage assigned tasks within budgeted hours and defined timelines. Qualification • Master’s degree in Life Sciences, Pharmacy, Medicine or related discipline. Experience • Relevant experience as a Medical Writer or Publication Project Coordinator in a medical communications or biopharmaceutical environment. Skills • Strong experience in scientific writing and publication planning. • Hands-on knowledge of Pub Connect and publication planning tools such as Datavision, Veeva Vault PromoMats or MedComms systems. • Understanding of journal and congress submission processes and regulatory guidelines. • Strong documentation, organizational and project management skills. • Ability to manage multiple workflows and coordinate with cross-functional and sponsor teams. • Strong communication and stakeholder management skills. About the Company Syneos Health® is a leading fully integrated biopharmaceutical solutions organization supporting clinical development, medical affairs and commercial functions worldwide, partnering with global life sciences companies to accelerate the delivery of therapies through innovation, collaboration and a people-centric culture.

Roles & Responsibilities • Manage end-to-end scientific writing and publication workflows using Pub Connect. • Create and maintain publication plans, author approvals, pre-submission queries and submission activities. • Assign and monitor workflows in Pub Connect with real-time updates on project status, versions and checklists. • Maintain accurate documentation from pre-kick-off through review cycles, sign-off and author approvals. • Capture and validate full publication plans and related documents in Pub Connect. • Coordinate journal submissions and congress activities. • Recommend appropriate target journals and manage pre-submission inquiries when required. • Perform dummy submissions to ensure readiness and review journal/congress websites for updated guidelines. • Collate metadata and prepare complete submission packages for journals and congresses. • Provide timely submission status updates to stakeholders. • Offer ad-hoc operational support including uploads in systems as required. • Create placeholders, upload versions, manage reference linking, anchoring and workflow monitoring. • Ensure compliance with journal/congress guidelines, SOPs, client standards and approved templates. • Perform online clinical literature searches as applicable. • Stay aligned with budgeted hours and communicate changes to medical writing leadership. • Complete administrative tasks within defined timelines. • Minimal travel as required (less than 25%). Qualification • Master’s degree in Life Sciences, Pharmacy, Medicine or related discipline. Experience • Relevant experience as a Medical Writer or Publication Project Coordinator in medical communications or biopharmaceutical environment. Skills • Strong experience in publication planning and scientific writing. • Hands-on knowledge of Pub Connect and publication planning tools such as Datavision, Veeva Vault PromoMats or MedComms systems. • Understanding of journal and congress submission processes and guidelines. • Strong documentation, organizational and project management skills. • Ability to coordinate with cross-functional and sponsor teams. • Strong attention to detail with ability to manage multiple projects simultaneously. • Good communication and stakeholder management skills. About the Company Syneos Health® is a fully integrated biopharmaceutical solutions organization operating across clinical development, medical affairs and commercial services, partnering with global life sciences companies to accelerate therapy development and delivery, with a strong global presence and a people-centric, inclusive culture.

Key Responsibilities• Diagnose and treat patients with musculoskeletal and spine-related problems• Conduct patient assessments and develop individualized rehabilitation plans• Deliver physiotherapy treatment as per clinic protocols• Educate patients on posture correction, exercises, and spine care• Monitor patient progress and update treatment plans accordingly• Maintain proper clinical documentation and records• Communicate treatment plans and recovery expectations clearly to patients• Work collaboratively with spine specialists and clinic staffTraining• Mandatory 1-month training at Bandra or Ghatkopar centerShift & Work Schedule• Morning Shift: 7:00 AM – 3:00 PM• Evening Shift: 1:00 PM – 9:00 PM• 6 working days per week, 1 weekly off• Flexibility with shifts is mandatoryQualifications• Bachelor’s in Physiotherapy (BPT) with completed 6-month internship• Master’s in Physiotherapy (MPT) preferredExperience• 0 – 1 year of experience in musculoskeletal physiotherapy• Freshers are welcome to applySkills Required• Strong knowledge of physiotherapy fundamentals• Excellent communication skills• Fluency in English is mandatory• Patient-focused and empathetic approach• Willingness to learn and follow structured rehabilitation protocolsBond Requirement• 1.5-year service bond is mandatory• Only candidates willing to sign the bond should applyAbout company:QI Spine Clinic is India’s first chain of clinics dedicated exclusively to spine rehabilitation. The clinic is known for its evidence-based, non-surgical approach to spine care and has been ranked #1 by the Times of India Survey for two consecutive years across Mumbai, Delhi, Gurgaon, Bangalore, and Pune.

Role & Responsibilities • Lead and manage medical writing assignments, including protocols, clinical study reports, regulatory documents, manuscripts, abstracts, and presentations • Mentor and supervise junior and mid-level medical writers, providing developmental feedback, training, and quality review • Ensure consistency, clarity, and scientific accuracy across all documents • Review and approve materials related to clinical trial registration (e.g., CTRI entries) and ethics committee submissions • Guide the team on best practices for literature review, referencing, and scientific integrity using sources like PubMed, NIH Library, and NLM databases • Provide strategic input on publication planning, conference material development, and stakeholder communications • Collaborate closely with cross-functional teams including researchers, project managers, and external consultants to align on deliverables • Maintain up-to-date knowledge of global regulatory writing standards (e.g., ICH-GCP, GPP3, CONSORT) • Recommend and implement process improvements, templates, and SOPs for documentation • Provide oversight for version control, formatting, and adherence to SOP MSCR/GEN/03-03 Qualification • PhD/MD/MPharm/MSc in Life Sciences, Medicine, or Pharmacy Experience • Minimum 10 years of medical writing experience, preferably in a CRO or clinical/preclinical research setting • Demonstrated experience managing or mentoring a team of writers • Strong command of written English and scientific communication • Proficiency with referencing tools (e.g., EndNote) and document management systems • Excellent organizational and project management skills Skills • Experience in preclinical (in-vitro/in-vivo) and clinical trial documentation • Exposure to publication strategy and submission to peer-reviewed journals • Familiarity with tools like CTD structure, CTRI submission portals, and regulatory publishing platforms About The Company • MS Clinical Research (MSCR) is a clinical research organization (CRO) focused on providing comprehensive services in medical writing, regulatory affairs, and pharmacovigilance.

Role & Responsibilities • Provide general medical care to IIT Jammu staff and students • Diagnose and treat a wide range of common illnesses and injuries • Offer medical consultations and health advice • Maintain medical records and ensure confidentiality • Provide first aid and emergency care when necessary • Assist in the development of health programs and initiatives at IIT Jammu • Coordinate with specialists and other healthcare professionals when necessary Qualification • MBBS (Bachelor of Medicine, Bachelor of Surgery) Experience • Experience in a clinical setting is preferred, but fresh graduates are also eligible to apply Age Limit • Minimum Age Limit: 21 years • Maximum Age Limit: 50 years Selection Process • Interview Compensation • Minimum Salary: ₹70,000/- per month • Maximum Salary: ₹80,000/- per month Application Fee • No application feeAbout The CompanyIIT Jammu (Indian Institute of Technology Jammu) is a premier educational institution in India that is part of the IIT system, renowned for its excellence in engineering, technology, and research.Last Date of Application02-02-2026Official NotificationClick Here

Roles & Responsibilities • Perform EDC programming using Medidata RAVE or Veeva EDC • Create, deploy, and maintain clinical study databases • Configure and test edit checks as per approved specifications • Review Database Specifications (DBS) and Data Validation Specifications (DVS) • Support database release activities for production environments • Ensure compliance with SOPs, GCP, ICH guidelines, and sponsor requirements • Provide technical support to Clinical Data Management (CDM) teams • Assist data managers with listings, reports, and operational tasks • Participate in internal and external study team meetings • Identify project risks and communicate status to stakeholders • Maintain high standards of quality, documentation, and performance Qualification • Degree in Life Sciences, Pharmacy, or related discipline Experience • 1–4 years of experience in clinical database design and deployment • Minimum 1+ year of hands-on EDC programming experience in Pharma, Biotech, or CRO • Practical experience with Medidata RAVE or Veeva EDC is mandatory Skills • Strong knowledge of EDC systems and clinical database programming • Understanding of drug development and clinical trial processes • Knowledge of clinical data management best practices • Familiarity with global clinical trial workflows and productivity targets • Good analytical, documentation, and problem-solving skills • Effective communication and team collaboration abilities About the Organisation Atorus Research is a specialized clinical analytics organization delivering high-efficiency, technology-driven solutions to simplify complex clinical trial data. The company supports global studies while ensuring strict compliance with GCP, ICH guidelines, and international regulatory standards.

Roles & Responsibilities• Visit patients at their residences and conduct dental consultations along with the team• Perform consultations using advanced digital and diagnostic technology• Manage patient records, appointments, and consultation details• Ensure high standards of patient care and clinical excellence• Participate in training programs provided by the organization• Commit to continuous learning and professional developmentWork Details• Home consultation radius: 5–10 km within assigned home zone• Working hours: 9-hour shift• Weekly off: Every Monday• Travel allowance provided in addition to salaryEligibility & Requirements• Qualification: BDS• Experience: 0–2 years (Freshers can apply)• Willingness to do home consultations• Good communication and patient-handling skills• Interest in technology-driven dental careBenefits• Health Insurance• Provident Fund• Leave Encashment• Other leave benefits as per company policyCompany:Clove Dental offers a technology-enabled, patient-centric work environment with structured training and growth opportunities for young dental professionals.