Doctor Jobs

Roles & Responsibilities• End-to-end ICSR case intake, processing, follow-up, and regulatory submissions• Provide medical review support and narrative writing• Perform MedDRA coding and case quality checks• Ensure compliance with global reporting timelines (FDA, EMA, MHRA)Qualification• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, or other Lifesciences degreeExperience• 4–6 years of relevant pharmacovigilance experienceSkills• Strong understanding of global pharmacovigilance regulations (ICH, GVP, FDA, EMA guidelines)• Experience with safety databases (Argus/ArisG preferred)• Strong analytical and documentation skills• Ability to work in a compliance-focused, quality-driven environmentAbout The CompanyMedifodil Smart Pharma Solutions is an expanding pharmacovigilance department offering high-growth opportunities in a quality-driven environment. With a focus on regulatory compliance and patient safety, Medifodil provides comprehensive solutions across ICSR, aggregate reporting, and PV Quality Assurance (QA).

Roles & Responsibilities• Deliver high-quality primary medical care to patients of all ages• Diagnose and manage common illnesses and chronic diseases• Conduct preventive health assessments and routine check-ups• Prescribe medications and monitor treatment outcomes• Refer patients to specialists and coordinate follow-up care• Maintain accurate EMR documentation in compliance with DHA guidelinesQualification• MBBS with GP or Family Medicine qualificationExperience• Minimum 2–4 years of relevant experienceSkills• Strong clinical judgment and a patient-focused approach• Excellent communication and interpersonal skills• Ability to manage a diverse patient population and provide comprehensive careAbout The CompanyFirst Medical Center is a leading outpatient clinic in Dubai, UAE, providing high-quality healthcare services with a focus on primary and preventive care. The center is committed to delivering comprehensive medical services and ensuring patient satisfaction and well-being through expert care.

Roles & Responsibilities• Conduct medical services and provide support to clinical teams• Manage and lead medical affairs and marketing strategies• Support the development of scientific publications and materials• Ensure compliance with regulatory guidelines in medical services• Collaborate with internal teams for product development and marketing• Provide medical and scientific expertise to support strategic initiativesQualification• MD – PharmacologyExperience• 0–3 yearsSkills• Strong knowledge in medical affairs and pharmacology• Excellent communication and interpersonal skills• Ability to interpret scientific data and apply it to medical services• Proficient in medical writing and scientific presentationsAbout The CompanyAlembic Pharmaceuticals Ltd. is a leading pharmaceutical company committed to providing high-quality products and services. With a strong presence in the medical industry, Alembic focuses on innovation and compliance, aiming to improve the lives of patients worldwide.

Roles & Responsibilities• Conduct medical evaluations and clinical assessments for study participants• Ensure subject safety and adherence to clinical trial protocols• Review and interpret clinical data and medical reports• Support BA/BE studies and clinical trial activities• Maintain compliance with ICH-GCP, DCGI, and regulatory guidelines• Collaborate with clinical research, QA, and operations teamsQualification• MBBSExperience• 0–3 YearsSkills• Strong knowledge of clinical trial protocols and ICH-GCP guidelines• Excellent communication and interpersonal skills• Ability to interpret clinical data and medical reports• Proficiency in using clinical research software and toolsAbout The CompanyNoah Therapeutics Pvt. Ltd. is a growing Clinical Research Organization (CRO) committed to quality, compliance, and innovation in the healthcare sector. We specialize in clinical trials, research, and testing, aiming to contribute to the medical field with high standards and expertise.

Roles & Responsibilities:• Lead and manage complex neuro-rehabilitation cases• Perform detailed clinical assessments and design evidence-based treatment plans• Deliver specialized physiotherapy interventions focused on neurological recovery• Monitor patient progress and optimize outcomes through individualized care• Collaborate with a multidisciplinary healthcare team• Maintain high standards of patient-centric rehabilitation servicesQualifications:• Master of Physiotherapy in Neurology – MandatoryExperience:• Minimum 3+ years of clinical experience in neuro-rehabilitationSkills :• Strong clinical assessment and diagnostic skills• Expertise in neurological physiotherapy and rehabilitation protocols• Excellent communication and teamwork abilities• Patient-focused approach with attention to quality outcomesBenefits:• Competitive and negotiable compensation based on expertise• Opportunity to work in a state-of-the-art clinical facility• Collaborative, growth-oriented, and professional work environmentAbout the Company:MnD Consultation Services Pvt. Ltd. is a professional healthcare recruitment and consultation firm supporting premier clinical facilities with highly skilled rehabilitation professionals, fostering excellence in patient care and clinical outcomes.

Roles & Responsibilities• Support research activities related to clinical studies.• Assist in organizing and conducting research trials.• Maintain accurate patient records and research documentation.Qualification• BDS/BAMS/BHMS/BUMS with PGDCR is mandatory.• Pharm D.Experience• Research experience in clinical or healthcare-related fields is desirable.Skills• Understanding of clinical research methodologies.• Ability to handle research documentation and patient data.• Strong communication and analytical skills.About The CompanyTata Memorial Centre is one of India’s leading research institutions focused on cancer care and research. The center plays a key role in educating healthcare professionals and advancing research for better cancer treatment.Last date of online application: 13/02/2026, up to 05:30 p.m.

Roles & Responsibilities• Assist in collecting and analyzing data for clinical studies.• Participate in the development and implementation of research protocols.• Help in managing patient data and ensuring accuracy in study records.Qualification• MBBS/BDS Degree.Experience• Research experience is desirable, with exposure to clinical studies.Skills• Knowledge of clinical research processes.• Strong organizational and data management skills.• Good communication and teamwork abilities.About The CompanyTata Memorial Centre offers a unique environment for advancing healthcare and research in India. The center is committed to delivering the highest standards of care and conducting pioneering research in oncology.

Roles & Responsibilities• Lead research activities in clinical studies and assist in managing research teams.• Collaborate with Principal Investigators to design and execute clinical trials.• Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.• Prepare reports and presentations for research findings.Qualification• MD/MS/DNB in medical specialties with 3 years of research experience or DM/MCh/Dr.NB.Experience• 3 years of clinical research experience in medical specialties.Skills• Expertise in clinical trial design and execution.• Knowledge of GCP guidelines and regulatory standards.• Strong analytical and leadership skills.About The CompanyTata Memorial Centre is dedicated to advancing cancer treatment and research, serving as a global leader in the field of oncology. The center integrates research with education, providing comprehensive care to patients.

Roles & Responsibilities:• Lead complex neuro-rehabilitation cases with a focus on evidence-based recovery• Conduct detailed clinical assessments and develop individualized treatment plans• Implement specialized physiotherapy interventions to improve patient outcomes• Work collaboratively with a multidisciplinary healthcare team• Maintain accurate patient records and monitor progress• Provide patient-centric care to support rehabilitation goalsQualifications:• Master of Physiotherapy (MPT) in Neurology – MandatoryExperience:• Minimum 3+ years of clinical experience in neuro-rehabilitationSkills:• Strong clinical assessment and decision-making abilities• Patient-focused approach to treatment• Excellent communication and teamwork skills• Ability to manage complex rehabilitation cases• Professional and ethical practiceAbout the Company:MnD Consultation Services Pvt. Ltd. is dedicated to delivering high-quality rehabilitation services through advanced clinical practices and a collaborative work culture. The organization offers a state-of-the-art facility focused on improving patient outcomes and supporting professional growth.

Roles & Responsibilities• Drive scientific excellence in the rapidly evolving Hepatology space• Engage with key opinion leaders and healthcare professionals• Support evidence-based clinical practice with robust scientific communication• Collaborate with cross-functional teams to deliver medical insights and strategic supportQualification• MBBS / MD (Pharmacology)Experience• Freshers and experienced candidates are welcome to applySkills• Strong scientific communication• Collaboration skills• In-depth knowledge in Hepatology• Ability to engage and work with healthcare professionals and key opinion leadersAbout The CompanyDr. Reddy’s Laboratories is a global pharmaceutical company, dedicated to providing high-quality medicines in the form of innovative solutions for patients worldwide. Dr. Reddy’s Laboratories focuses on bringing science and medicine together to improve patient care.

Roles & Responsibilities:• Liaise with business partners, country medical teams, and medical leads• Maintain strong relationships with internal stakeholders across regions• Coordinate regularly with FMV leads and tier validators• Ensure accurate transfer of HCP data into tiering systems• Perform data quality checks and remediation of identified errors• Prepare monitoring, verification, and compliance reports within timelines• Support quarterly scientific expert and customer engagement reporting• Manage and prioritize requests via centralized mailbox/platform• Review HCP and non-HCP tiering documentation• Analyze expert credentials to determine appropriate tier levels and FMV• Support local process training, tools, and continuous improvementsQualification:• Bachelor’s or Master’s degree required• B.Pharm / M.Pharm / Life Sciences preferredExperience:• 1–2 years of experience in pharma or life-science companiesSkills:• Strong proficiency in MS Excel, Word, PowerPoint, Outlook, Access• Experience in data handling, reporting, and documentation• Stakeholder and project management skills• Strong communication (written & spoken English)• Analytical thinking, planning ability, and teamwork mindsetAbout The Company:Sanofi is a global pharmaceutical leader, centralizing and streamlining global medical processes to reduce dependency on external vendors and strengthen internal expertise. The company focuses on improving the quality of life for patients worldwide by delivering innovative medicines and therapies. Sanofi offers an inclusive, diverse, and equal-opportunity workplace with structured career growth and skill development opportunities.

Roles & Responsibilities:• eCRF development, testing, and maintenance• Clinical data validation and query management• Preparation of CDM documentation (DMP, DVP, eCCG)• Data reconciliation activities and user training• Medical coding using standard dictionaries• Handling EDC systems and related tools (IWRS, ePRO)• Supporting end-to-end clinical data management activitiesQualification:• M.Pharm (Pharmacology / Quality Assurance)• BDS / BAMS / BHMSExperience:• Site-level experience as a Clinical Research Coordinator (CRC)• Hands-on experience in late-phase clinical trials• Working knowledge of EDC systems and CDM processes• Exposure to IWRS, ePRO, and clinical data toolsSkills:• Strong knowledge of clinical data management processes• Proficiency in handling eCRFs, IWRS, and ePRO systems• Expertise in medical coding using standard dictionaries• Strong analytical and problem-solving skills• Excellent communication and training skillsAbout The Company:Lambda Therapeutic Research Ltd. is a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad. Lambda operates across India, USA, Canada, UK, Spain, and Poland, offering clinical research services with a focus on late-phase clinical trials. With competitive compensation and global exposure, Lambda provides a structured career growth path in the clinical research industry.

Roles & Responsibilities:• Perform systematic literature searches for regulatory and scientific documents• Assist in preparing pre-clinical and clinical sections of Marketing Authorization Dossiers (CTD/eCTD)• Support toxicology documentation including PDE, OEL, and other risk assessments• Contribute to medical-scientific documents such as publications, product rationales, and medico-marketing materials• Collaborate closely with senior medical writers and regulatory managers• Handle additional responsibilities aligned with role capabilitiesQualification:• Degree in Pharmacy, Life Sciences, or related disciplineExperience:• FreshersSkills:• Strong interest in medical writing and regulatory affairs• Basic understanding of EU marketing authorization procedures• Awareness of economic principles related to healthcare/pharma• Excellent written and spoken English communication skills• Proficiency in MS Word, Excel, PowerPoint, and scientific literature review• Ability to work independently with high accuracy and attention to detail• Strong teamwork, responsibility, and interpersonal skillsAbout The Company:Cencora offers global exposure in regulatory medical writing. The company provides structured training and mentorship for early-career professionals, working on international regulatory submissions. With a commitment to an inclusive and equal opportunity workplace, Cencora offers competitive compensation and long-term career growth opportunities within its global ecosystem.

Role & Responsibilities• Conduct research activities as per approved project protocols• Assist in clinical evaluation, data collection, and analysis• Prepare and maintain research documentation and reports• Ensure compliance with ethical guidelines and institutional SOPs• Coordinate with investigators and research team members• Support project execution, monitoring, and timely reportingQualification• MBBS/BDS/MD/MDSVacancies No• 01Experience• Relevant clinical or research experience preferred• Experience in medical or research institute setting desirableSkills• Strong research and clinical knowledge• Documentation and scientific reporting skills• Good analytical and data interpretation abilities• Effective communication and teamwork skills• Understanding of research ethics and complianceAge Limit• Minimum age: 21 years• Maximum age: 40 yearsSelection Process• InterviewApplication Fee• No application feePay Scale• ₹80,000 – ₹96,000 per monthAbout the CompanyPostgraduate Institute of Medical Education and Research is a premier medical and research institute of national importance in India, renowned for excellence in patient care, advanced medical education, and high-quality biomedical research. The institute plays a key role in advancing clinical research and healthcare standards through innovation, ethics, and multidisciplinary collaboration.Last date to apply: 19-02-2026Official Notification and Application Form - Click Here

Roles & Responsibilities• Oversee receipt, processing, and reporting of adverse events from clinical trials and post-marketing sources• Ensure timely and compliant submission of expedited and non-expedited safety reports to clients and regulators• Process and support preparation of ICSRs, SAEs, DSURs, PSRs, Annual IND reports, and aggregate safety reports• Maintain and work within safety databases as per Fortrea or client-specific conventions• Support reconciliation of safety databases and workflow monitoring to meet project timelines• Participate as safety lead on assigned projects and support cross-functional collaboration• Prepare safety presentations, metrics, status reports, and quality documentation• Support audits, inspections, TMF activities, and Safety Committees/DSMB data preparation• Assist in development of SOPs, WIs, Safety Management Plans, and study-specific training materialsQualification• Non-degree / Associate / Bachelor’s / Master’s / PharmD in Life Sciences, Pharmacy, Nursing, Biological Sciences, Chemistry, or related fields• Equivalent relevant industry experience may be consideredExperience• 1–5+ years of Pharmacovigilance/Safety experience depending on qualification• Hands-on experience in AE/SAE processing, safety databases, narratives, and regulatory submissionsSkills• Strong knowledge of Pharmacovigilance processes and global safety reporting requirements• Understanding of GCP, ICH guidelines, and worldwide regulatory requirements• Knowledge of medical and drug terminology• High attention to detail, strong communication, and organizational skills• Proficiency in MS Office and safety systems• Team-oriented with problem-solving and decision-making abilityAbout the OrganizationFortrea is a global Contract Research Organization (CRO) delivering clinical development, pharmacovigilance, and regulatory services. The company partners with life sciences organizations worldwide to ensure patient safety, regulatory compliance, and high-quality clinical outcomes.

Roles & Responsibilities• Perform quality review of safety cases, regulatory documents, and pharmacovigilance reports• Compile quality metrics, identify trends, and support client quality reviews• Assist in CAPA preparation, implementation, and effectiveness monitoring• Review adverse events, product quality complaints, and medical information cases within timelines• Support audit readiness, regulatory inspections, and quality management activities• Conduct data analysis and contribute to process improvement initiatives• Assist in training coordination, documentation review, and QC activities• Support reconciliation of safety data and regulatory documentation complianceQualification• Bachelor’s / Master’s / PhD in Medicine, Pharmaceutical Sciences, Life Sciences, Nursing, or related disciplineExperience• Minimum 2+ years of experience in Pharmaceutical, Biotechnology, or CRO industry• Experience in Pharmacovigilance, Safety Writing, or Quality Review preferredSkills• Knowledge of Pharmacovigilance processes and safety reporting requirements• Understanding of GCP, GVP, ICH, EU, and FDA regulatory guidelines• Strong attention to detail and documentation review skills• Good analytical, communication, and problem-solving abilities• Proficiency in MS Office and safety data management toolsAbout the OrganizationFortrea is a global Contract Research Organization (CRO) providing clinical development, pharmacovigilance, and regulatory support services. The company partners with life sciences organizations to deliver high-quality, compliant solutions that improve patient safety and accelerate drug development.

Roles & Responsibilities• Provide comprehensive general practice care across acute, chronic, and preventive health• Inherit and manage an established full patient book due to GP retirement• Deliver mixed-billing consultations with flexibility in appointment structure• Maintain accurate and compliant clinical documentation• Work collaboratively with experienced practice nurses, admin staff, and leadership• Exercise full clinical autonomy in patient management and care deliveryQualification• Fellowship with RACGP and/or ACRRM• Vocational Registration (VR) as a General Practitioner• Unrestricted AHPRA registration• Medical Indemnity InsuranceExperience• Suitable for experienced VR GPs seeking long-term stability• Comfortable managing 4–5 patients per hour in a community clinic settingSkills• Strong clinical judgement and patient communication skills• Ability to build long-term patient relationships• Independent decision-making with a collaborative mindset• Commitment to continuity and quality of careAbout the RecruiterCornerstone Medical Recruitment (CMR) specialises in placing medical professionals into high-quality, well-supported healthcare roles across Australia.

Role & Responsibilities• Deliver comprehensive general practice services including chronic disease management, health assessments, immunisations, women’s health, and acute presentations• Provide high-quality, community-focused, patient-centred care• Work collaboratively with on-site nursing, allied health, and admin teams• Maintain accurate and compliant clinical documentation• Opportunity to develop and grow a special interest area if desired• Use Best Practice clinical software with Cubiko analytics and HotDoc online bookingsQualification• Full registration with AHPRA• Vocational Registration (VR) or equivalent• Medical Indemnity Insurance• Valid Working with Children CheckExperience• Suitable for experienced VR GPs and GPs seeking contract/temporary roles• Comfortable managing a broad GP caseload in a busy community clinicSkills• Strong clinical decision-making and patient communication skills• Ability to work independently within a multidisciplinary team• Commitment to preventative, integrated healthcare delivery• Interest in community health and continuity of careAbout the CompanyLatrobe Community Health Service is a not-for-profit community health organisation delivering integrated healthcare services across Victoria. With strong roots in Gippsland and growing metro services, Latrobe focuses on prevention, early intervention, and holistic community wellbeing.

Roles & Responsibilities• Teach Pharmacology to BDS students through lectures, tutorials, and practical sessions as per prescribed curriculum• Guide students on rational drug use, prescription writing, and pharmacology relevant to dental practice• Prepare lesson plans, teaching materials, and academic schedules• Conduct internal assessments, evaluations, and assist in university examinations• Maintain academic records, attendance, and assessment documentation• Participate in departmental academic activities, seminars, and curriculum development• Engage in research activities, publications, and scholarly work (preferred)• Ensure compliance with DCI/NMC norms and university regulations• Support overall academic growth and quality standards of the institutionQualification• MD in Pharmacology from a recognized medical college as per NMC/DCI norms• Valid State Medical Council / NMC registrationExperience• Relevant teaching experience as per the designation norms prescribed by NMC/DCI• Research and publication exposure is preferredSkills• Strong subject knowledge in Pharmacology• Effective teaching, presentation, and communication skills• Ability to mentor and guide undergraduate dental students• Academic planning, documentation, and assessment skills• Research orientation and publication interest• Commitment to regulatory compliance and academic excellenceAbout the OrganizationThe institution is committed to delivering quality dental education aligned with national regulatory standards, focusing on academic excellence, research, and holistic professional development of students.