Doctor Jobs

Role & Responsibilities • Exchange and disseminate scientific, educational and research-related information to healthcare professionals • Engage proactively and reactively with Thought Leaders (Doctors) as a scientific partner • Provide education on study protocols, abstracts, literature and product-related scientific data in compliance with regulations • Respond to unsolicited off-label medical queries as per local compliance guidelines • Coordinate with Medical Societies and participate in Advisory Boards • Organize and support scientific education programs and training sessions • Attend congresses and conventions, establish new KOL relationships and gather competitive intelligence • Identify, profile and segment Thought Leaders and support engagement planning aligned to Medical Affairs strategy Qualifications  • MD / MBBS / BDS / MDS qualificationExperience • Minimum 1+ year experience in Medical Affairs / Clinical Operations / MSL role preferred • Basic knowledge of Diabetes, Chronic Kidney Disease, Oncology therapy areas • Understanding of clinical trial design and rationale • Strong communication and presentation skills • Ability to work independently and in a collaborative team environment Skills • Scientific communication and KOL engagement • Medical education program coordination • Advisory board and congress participation • Data interpretation and evidence-based discussion • Presentation and stakeholder management skills • Competitive intelligence gathering • MS Office and documentation skills About the Company • Bayer is a global life-science company with core competencies in healthcare and agriculture • Known for innovation in pharmaceuticals, consumer health and crop science

Role & Responsibilities • Execute medical affairs strategy for the assigned geographic zone • Understand disease trends, treatment practices and therapeutic needs through KOL engagement, scientific meetings and journal reviews • Disseminate credible, non-promotional scientific information to internal and external stakeholders • Execute medical projects including IIS (Investigator Initiated Studies) • Support medico-marketing strategies and provide regular field insights to management • Identify and develop relationships with Key Opinion Leaders and Expert Experts (EEs) • Support registration of new products and indications by providing medical rationale, literature support and scientific presentations • Support defence of marketed products with regulators, NGOs and media as required • Write, review and revise labeling and scientific documentation as per SOPs • Support regulatory affairs activities and stakeholder engagement Qualifications • Medical degree (MD preferred, Pharmacology specialization preferred) or life sciences qualification Experience• 0–3 years of experience in Medical Affairs / Pharmaceutical / Healthcare industry (fresh MD Pharmacology graduates can apply) • Candidates without doctoral qualification require 10+ years of relevant field-based scientific experience • Strong scientific knowledge of Diabetes therapy area • Good interpersonal and communication skills Skills • Scientific communication and presentation skills • KOL relationship management • Medical writing and documentation skills • Analytical and field-insight generation ability • Basic IT proficiency (MS Office) • Ability to work independently in field medical roles About the Company • Boehringer Ingelheim is a global biopharmaceutical company active in human and animal health

Roles & Responsibilities•Draft new and revised Pharmacovigilance Agreements (PVAs) as per company and regulatory requirements •Review PVAs to ensure quality, accuracy, and global pharmacovigilance compliance •Address internal and collaborating company comments on PVAs •Manage and monitor the dedicated PVA mailbox •Announce new and revised PVAs to relevant stakeholders •Maintain and update global PVA trackers and reconciliations •Perform compliance monitoring of effective PVAs and prepare dashboards •Support Project Managers in maintaining project documents and trackers •Upload, archive, and maintain PVAs in the company repository •Participate in team meetings and provide regular status updatesQualifications•B.Pharm, M.Pharm, B.Sc, M.ScExperience •Minimum 3-7 years of hands-on experience in Pharmacovigilance•Prior experience in drafting and managing Global and Local Pharmacovigilance AgreementsSkills •Strong knowledge of ICH & GVP regulations•PVA drafting and management •Life sciences domain expertise•Documentation skills•Stakeholder coordination•Good communication skillsAbout the CompnayTata Consultancy Services (TCS) is a global leader in IT services, consulting, and business solutions, headquartered in India and part of the Tata Group. With operations in over 50 countries, TCS serves clients across industries including life sciences, healthcare, pharmaceuticals, banking, and manufacturing. The company is known for its strong focus on innovation, digital transformation, regulatory-compliant solutions, and employee development, delivering high-quality services that help organizations improve efficiency, compliance, and business performance worldwide.

Role & Responsibilities • Lead and execute medical affairs objectives for assigned therapeutic areas • Act as an internal medical and scientific resource for AbbVie products and disease areas • Build and maintain professional relationships with KOLs, academic centres and researchers • Present clinical and scientific data to healthcare professionals and institutions • Support clinical research initiatives in collaboration with R&D and Clinical Operations • Contribute to development of disease-state and product communication materials • Support advisory boards, round table meetings and scientific forums • Provide ongoing training to sales, medical affairs and internal stakeholders • Ensure accurate documentation of field medical activities • Maintain compliance with regulatory, ethical and internal company policies • Support pharmacovigilance, HEOR and global medical office activities • Collaborate closely with commercial and medical leadership teams • Travel extensively for field engagement (approximately 60% field time) Qualifications & Experience • MD / MBBS / PharmD • Minimum 2–3 years of experience in Medical Affairs or pharmaceutical / clinical research roles • Experience working in cross-functional and matrix organizations • Strong ability to interpret and communicate clinical data effectively Skills • Excellent scientific communication and presentation skills • Strong analytical and data interpretation abilities • Relationship building and stakeholder engagement expertise • Strategic thinking and planning capability • Proficiency in Microsoft Office and digital tools • Ability to learn quickly and convey complex medical information clearly About the Company • AbbVie is a global biopharmaceutical company focused on discovering and delivering innovative medicines • Core therapeutic areas include immunology, oncology, neuroscience and eye care

Role & Responsibilities • Plan and execute scientific field activities for Rare Blood Disorders with focus on Hemophilia • Engage healthcare professionals through scientific discussions and evidence-based communication • Disseminate clinical study data, treatment guidelines and recent medical updates • Organize scientific meetings, CMEs and expert lectures in the therapeutic area • Support clinicians in diagnosis and management of hemophilia patients • Provide guidance on patient management pathways and real-world challenges • Collaborate in speaker training programs and scientific education initiatives • Collect field insights, treatment trends and share inputs for medical strategy • Align scientific field activities with company’s medical and brand strategies Qualifications • MBBS / MD or advanced scientific/medical degree Experience• 2–4 years of experience in Medical Affairs / MSL role • Prior experience in Hematology / Hemophilia is strongly preferred Skills • Strong scientific communication and presentation skills • Ability to engage and build long-term relationships with HCPs and KOLs • Knowledge of rare blood disorders, hemophilia and treatment guidelines • Strategic planning, analytical thinking and data interpretation abilities • Excellent interpersonal, teamwork and stakeholder management skills • Proficiency in English About the Company • Sanofi is a global healthcare leader dedicated to discovering, developing and delivering innovative medicines • The company focuses on advancing science in areas including rare diseases, vaccines, oncology and immunology

Role & Responsibilities • Provide strategic and tactical medical inputs to Product Management for ethical promotion of oncology products • Develop and support marketing and brand strategies through compliant medical–marketing programs • Review, approve and ensure regulatory compliance of promotional and educational materials • Develop, review and support clinical study protocols, NDAs and local/global clinical projects • Provide accurate, balanced and timely medical information to internal and external stakeholders • Lead and execute sales force training, including pre-launch and launch programs • Support new product planning, early access programs, market research and commercial evaluations • Provide medical expertise for product registrations, labeling, and adverse event reporting • Act as key medical liaison across functional teams and external stakeholders • Lead, mentor and manage Medical Affairs teams ensuring high performance and compliance • Support budgeting, provisioning and expense control for Medical Affairs operations Qualifications • Postgraduate degree in Pharmacology or other medical specialty OR Graduate degree in MedicineExperience• 6–8 years of Medical Affairs experience with minimum 3 years in Oncology • Prior experience in oncology new product launch is mandatory Skills • Strong knowledge of pharmaceutical medicine, clinical pharmacology and oncology therapeutics • Expertise in clinical trial design, methodology and regulatory compliance • Medical writing, presentation and scientific communication skills • Strong analytical, decision-making and medical judgment abilities • Excellent interpersonal, networking and stakeholder management skills About the Company • Dr. Reddy’s Laboratories is a leading global pharmaceutical company operating in 66+ countries • Founded in 1984, the company is driven by its mission of providing affordable and innovative medicines

Role & Responsibilities • Lead and execute global medical affairs strategy for assigned therapeutic area and priority assets • Develop and own the Integrated Evidence Plan (IEP) across early and late asset lifecycle stages • Drive evidence generation including Interventional Studies, Non-Interventional Studies (NIS), Real-World Evidence (RWE) and implementation science projects • Define and implement global Medical Science Liaison (MSL) strategy and medical education programs • Lead scientific publication planning and Medical Expert/KOL network development • Represent Global Medical Affairs with internal stakeholders and external regulatory, investment and medical communities • Review and manage Managed Access Program (MAP) requests and define global treatment strategies • Develop Post Study Drug Supply (PSDS) treatment plans ensuring regulatory and safety compliance • Collaborate cross-functionally with Clinical Development, Regulatory, Market Access and Commercial teams Qualifications & Experience • MD preferred / PhD / PharmD in Health Sciences • Minimum 10 years of experience in Medical Affairs and/or Clinical Development within the pharmaceutical industry • Strong knowledge of GCP, clinical research methodology, protocol design and regulatory requirements • Proven experience in early asset lifecycle, pre-launch and launch medical strategy • Strong critical thinking, leadership and stakeholder management skills • Excellent written and verbal English communication skills Skills • Medical Affairs Strategy • Integrated Evidence Planning • Real-World Evidence (RWE) • Clinical Research & GCP Compliance • KOL Engagement & Medical Education • Publication Planning • Cross-Functional Leadership • Regulatory & Safety GovernanceAbout the Company • Novartis is a leading global innovative medicines company headquartered in Basel, Switzerland • It focuses on discovering, developing, and delivering breakthrough treatments across areas such as oncology, cardiovascular, neuroscience, immunology, and rare diseases

Role & Responsibilities • Support initiation, execution, monitoring, and follow-up of clinical studies and medical projects within oncology therapeutic area • Develop and deliver training PPTs, CMEs, and conference scientific materials based on updated clinical guidelines and recent evidence • Identify and engage Key Opinion Leaders (KOLs), expert speakers, and academicians for scientific programs • Create educational programs, scientific content, and disease awareness initiatives • Manage all medical and educational content related to assigned oncology products and disease states • Collaborate closely with marketing and sales teams to support medical strategy and execution • Review and approve promotional and local packaging materials as per SOPs and regulatory standards • Participate in interdisciplinary medical and commercial projects • Gather field insights from KOLs and submit strategic reports to Head Office for brand planning • Conduct medical trainings for field teams and address scientific queries • Maintain strong pharmacology and therapeutic knowledge in oncology Qualifications & Experience • Pharm D / B.Pharm / M.Pharm / MBBS / MD / BDS • Minimum 5 years of experience in Medical Affairs (mandatory) • 5–10 years of overall professional experience • Willingness for international travel as required Skills • Oncology medical affairs expertise • Scientific communication & KOL management • CME & training content development • Medical writing and guideline interpretation • Promotional material review & compliance • Cross-functional collaboration • Pharmacology knowledge • Presentation & communication skills • Strategic reporting & field insight analysisAbout the Company • Hetero is a fast-growing pharmaceutical company focused on delivering innovative oncology solutions across emerging and regulated markets

Role & Responsibilities • Handle and process adverse event and serious adverse event reports from clinical trials and post-marketing sources • Determine appropriate action plans for incoming safety calls and reports • Collect, process, track, and document safety cases accurately • Prepare detailed safety narratives and reports • Maintain safety databases and track case follow-ups • Collaborate with internal teams and clinical research sites to ensure safety compliance • Support regulatory compliance and safety reporting activities • Maintain accurate safety documentation and timelines Qualifications & Experience • Bachelor’s degree in Nursing, Pharmacy, Pharmacology, or Healthcare-related discipline • Clinical experience or Pharmacovigilance / Clinical Research experience preferred • Proficient English communication skills • Strong knowledge of medical terminology • Proficiency in Microsoft Office tools Skills • Pharmacovigilance case processing • Adverse event reporting and safety documentation • Safety database management • Medical terminology and narrative writing • Regulatory compliance and GCP understanding • Attention to detail and time management • Strong communication and coordination skills About the Company • Medpace is a global Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries across 40+ countries

Role & Responsibilities • Process and review Individual Case Safety Reports (ICSRs) from multiple sources including literature, affiliates, and health authorities • Perform case triage, data entry, MedDRA coding, causality, seriousness, and expectedness assessment • Prepare medically accurate case narratives and perform quality checks • Manage follow-ups, reconciliation, and compliance tracking for safety reporting • Support expedited and periodic safety report submissions to regulatory authorities • Maintain regulatory databases and support product lifecycle management activities • Perform literature searches and maintain validated search strategies • Support audits, inspections, and compliance documentation • Collaborate with global PV teams and mentor junior team members Qualifications • Degree in Life Sciences / Health / Biomedical Sciences • Medicine, Dentistry, Nursing, Physiotherapy background is an added advantage • JLPT N2 or above (Japanese language proficiency) Experience • Prior experience in Pharmacovigilance / Drug Safety preferred • Experience with PMDA safety reporting and Japanese PV operations preferred Skills • Pharmacovigilance operations and ICSR processing • MedDRA coding and safety database handling • Japanese (JLPT N2+) and English communication • Regulatory compliance (ICH, EMA, PMDA, global PV regulations) • Literature review and safety data analysis • Quality control and audit readiness • MS Office and safety database proficiency • Analytical, documentation, and time management skills About the Company • Parexel is a global clinical research organization delivering clinical trials, regulatory, consulting, and market access services to advance life-changing therapies worldwide

Role & Responsibilities:Conduct detailed patient consultations and assess aesthetic and cosmetic concernsDesign and implement personalized treatment plans based on patient needsPerform advanced aesthetic and cosmetic procedures including PRP, GFC, and hair regrowth therapiesDeliver skin treatments such as HydraFacial, chemical peels, skin brightening and whitening proceduresManage anti-aging treatments, acne care, and scar managementCarry out laser hair reduction and skin rejuvenation treatmentsAdminister Botox, fillers, and non-surgical aesthetic procedures if certifiedProvide pre-treatment and post-treatment counselling and follow-up careMaintain accurate and timely documentation in the Hospital Management System (HMS)Educate patients about treatment options, benefits, precautions, and expected outcomesStay updated with the latest developments in cosmetology and aesthetic medicineWork closely with doctors and clinical staff to ensure seamless and high-quality patient careQualifications:BHMS or BDS from a recognized institutionCertification or diploma in cosmetology or aesthetic medicine will be an added advantageExperience:1–2 years of relevant experience in clinical cosmetology or aesthetic treatmentsSkills:Strong communication and interpersonal skillsPatient-centric and empathetic approachAbility to explain procedures clearly and build patient trustProficiency in handling advanced aesthetic equipment and technologiesAttention to detail and commitment to clinical excellenceAbout the Company:H-Cura is a fast-growing multi-specialty healthcare brand with expertise in Homeopathy, Advanced Hair & Skin Care, and Dental services. With an expanding network of clinics across Chennai and Bangalore, H-Cura is committed to delivering patient-centric, holistic, and result-driven healthcare solutions through modern infrastructure, advanced technology, and experienced medical professionals.

Role & Responsibilities • Engage scientifically with oncologists and key opinion leaders (KOLs) to build strong professional relationships • Conduct scientific discussions and medical education programs for healthcare professionals • Provide medical and scientific input to brand strategy and lifecycle management • Support Phase IV clinical studies and real-world evidence initiatives • Communicate clinical data, safety information, and product updates accurately • Collaborate with cross-functional teams including marketing, sales, and clinical research • Ensure all medical activities comply with regulatory and internal compliance standards Qualifications • MBBS with post-graduate qualification (MD / DM preferred) • Strong scientific acumen in oncology Experience • 1–2 years of experience in Oncology Medical Affairs / MSL role Skills • Scientific engagement and KOL management • Medical communication and presentation skills • Oncology domain expertise • Clinical data interpretation • Phase IV and real-world evidence support • Cross-functional collaboration • Compliance and ethical medical practice About the Company • IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, supporting life sciences organizations in driving innovation and improving patient outcomes worldwide

Role & Responsibilities:• Act as the primary clinical expert and liaison between the company and healthcare professionals• Conduct hands-on clinical training sessions and workshops for physiotherapists, clinicians, hospital staff, and internal sales teams• Deliver on-site and virtual product demonstrations during pre-sales and post-sales phases• Provide clinical guidance on equipment setup, protocol customization, and integration into rehabilitation programs• Support onboarding of new customers and ensure effective adoption and utilization of products• Assist the sales team during client meetings by addressing clinical queries and supporting product presentations• Contribute to tender documentation by providing clinical justification and evidence-based inputs• Participate in trade shows, conferences, CMEs, and product launch events• Build and maintain strong relationships with key clinical stakeholders and decision-makers• Serve as the main point of contact for clinical feedback, troubleshooting, and advanced product usage• Monitor customer satisfaction and support long-term customer retention• Support clinical research activities including case studies, outcome data collection, and reports• Organize and deliver educational content for workshops, webinars, and CME programs• Stay updated with the latest rehabilitation trends, treatment protocols, and competing technologies• Collaborate with product management and R&D teams to provide feedback for product enhancement• Assist in developing training materials, user manuals, and standardized clinical protocols• Work with marketing teams to create evidence-based content and clinical case studiesQualification:• Bachelor’s or Master’s Degree in Physiotherapy (BPT / MPT)• Specialization in Orthopaedic, Neurological, or Cardio-Pulmonary Rehabilitation is an added advantageExperience:• 2 to 5 years of clinical experience in physiotherapy or rehabilitation• Prior experience in medical devices, product training, or clinical support roles preferredSkills Required:• Strong knowledge of physiotherapy principles and rehabilitation techniques• Expertise in product demonstrations and clinical training• Excellent presentation, communication, and interpersonal skills• Ability to train, guide, and influence clinicians and healthcare professionals• Problem-solving mindset with a customer-focused approach• Willingness to travel locally and nationally as required• Proficiency in Microsoft Office and basic digital toolsBenefits:• Health insurance• Provident Fund• Cell phone reimbursementAbout the Company:Cnergy Ortho Care (P) Ltd is a healthcare solutions company specializing in advanced physiotherapy and rehabilitation equipment. The organization partners with healthcare professionals to improve clinical outcomes through innovative technology, hands-on training, and evidence-based rehabilitation solutions, while fostering strong clinical relationships and continuous product advancement.

Role & Responsibilities:• Work independently as a consultant physiotherapist on a sharing basis• Conduct patient assessments, diagnostic evaluations, and clinical examinations• Develop and implement individualized treatment and rehabilitation plans• Manage patient follow-ups and monitor progress outcomes• Maintain accurate clinical records and adhere to professional and ethical standards• Independently handle clinic operations during initial months without an assistant• Manage branch operations independently after the initial onboarding period• Build and maintain strong patient relationships through effective communication• Contribute to clinic growth by maintaining high-quality patient careQualifications:• Bachelor’s or Master’s Degree in Physiotherapy• Valid registration with relevant Physiotherapy Council or AssociationExperience:• Experience in independent physiotherapy practice preferred• Freshers with strong confidence and clinical skills may also be consideredSkills Required:• Diagnostic evaluation and clinical assessment skills• Strong communication and patient management skills• Ability to work independently and take responsibility for patient care• Record keeping and professional documentation skills• Self-motivation and confidence in independent clinical practiceAbout the Company:Akayda is an emerging healthcare organization focused on establishing accessible and patient-centric physiotherapy services through well-equipped clinics and professional support systems. The organization enables physiotherapists to practice independently while providing operational infrastructure, marketing assistance, and long-term growth opportunities within a growing healthcare network.

Role & Responsibilities • Perform primary medical review of safety cases, including assessment of seriousness, listedness/labeling, causality, adverse event coding, and medical narrative review • Update and document daily case data and case feedback in designated trackers and workflow management tools • Take full ownership of assigned deliverables while meeting quality, compliance, productivity SLAs, and KPIs • Provide medical guidance and training to case processing teams after completion of one year of tenure • Support aggregate review and signal detection activities related to single case processing • Ensure high standards of customer service and contribute to a culture of quality and accountability Qualifications • Bachelor’s degree in Medical Sciences OR MD / DO or equivalent medical degree • Relevant and equivalent experience may be considered in lieu of formal education Language Requirements • Speaking: English – ILR Level 3+ or higher • Reading/Writing: English – ILR Level 4+ or higher Experience • Working knowledge of medical sciences, diagnosis, therapeutics, drug treatments, and clinical procedures • Understanding of regulatory requirements related to Clinical Research • Knowledge of ICH-GCP guidelines Preferred Qualifications • 1–2 years of clinical practice experienceSkills • Pharmacovigilance and ICSR processing • Medical case review and safety assessment • Adverse event coding and narrative writing • Signal detection and aggregate review • Regulatory compliance (ICH-GCP) • Clinical research knowledge • Documentation and workflow management • Communication and training skills About the Company • Fortrea is a global Contract Research Organization (CRO) delivering clinical development, patient access, and pharmacovigilance solutions to biopharmaceutical and medical device companies worldwide

Role & Responsibilities • Act as the main point of contact (POC) for assigned clinical trial protocols within the country • Manage end-to-end execution of assigned clinical studies from feasibility to close-out • Ensure compliance with ICH-GCP, country regulations, company SOPs, and quality standards • Monitor study performance, timelines, deliverables, and recruitment targets • Review monitoring visit reports and escalate performance and training gaps • Conduct quality control visits as required • Lead and train local study teams and support CRAs as protocol experts • Develop and implement local risk management plans • Ensure compliance with CTMS, eTMF, and other clinical systems • Collaborate with investigators, CROs, and outsourcing partners • Represent the company to investigators and external stakeholders • Support budget management, contract approvals, and regulatory coordination • Collaborate with HQ, pharmacovigilance, medical affairs, and regional teams • Share best practices and support strategic planning initiatives Qualifications • Bachelor’s degree in Science or equivalent • Master’s / MD / PhD preferred • Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial operations Experience • 5–6 years of clinical research experience • Prior CRA experience preferred • Proven experience in managing multi-site or multi-country clinical studies Skills • Clinical trial project management • Site management and monitoring • Regulatory compliance and submissions • Risk management and quality control • CTMS and eTMF systems • Leadership and team coordination • Communication and stakeholder management • Conflict resolution and decision-making • Resource allocation and strategic planning About the Company • MSD is a global biopharmaceutical leader dedicated to discovering, developing, and delivering innovative medicines and vaccines that help improve health and save lives worldwide

Role & Responsibilities • Evaluate and diagnose dermatological conditions through clinical assessment   and patient history • Prescribe appropriate medical and cosmetic treatments • Perform non-invasive dermatology and aesthetic procedures • Educate patients on treatment plans, lifestyle modifications, and preventive skin   care • Conduct follow-up consultations and monitor treatment progress • Maintain accurate clinical documentation and patient records • Manage complex dermatological cases and provide patient-centered care • Participate in clinical research and contribute to medical advancements Qualifications • MBBS / MBChB or equivalent from a recognized institution • MD Dermatology or equivalent specialty qualification recognized by DHA / HAAD /   MOH UAE • Valid or eligible DHA Specialist Dermatology license • Certification in BLS and ACLS Experience • Minimum 5–10 years of specialist-level dermatology experience • Proven experience in medical and cosmetic dermatology • Experience in managing chronic and complex skin conditions Skills • Medical and cosmetic dermatology expertise • Non-invasive aesthetic procedures • Patient counseling and education • Clinical documentation and EMR usage • Communication and interpersonal skills • Team collaboration and adaptability • Time management and decision-making About the Company • Al Futtaim Private Company (LLC) is a leading healthcare and retail conglomerate   in the UAE known for delivering high-quality, patient-focused medical services   across multiple specialties

Role & Responsibilities • Coordinate cancer research projects and epidemiology programs • Support investigators in planning, execution and monitoring of research studies • Maintain study documentation, reports and regulatory records • Coordinate patient follow-ups and data collection activities • Ensure compliance with ethical, institutional and regulatory guidelines • Assist in data analysis, reporting and project presentations • Liaise with multidisciplinary clinical and research teams • Maintain accurate project timelines and communication logs Qualifications & Experience • MBBS / BDS / BAMS / BHMS from a recognized institution • Age limit: 21 – 35 years Skills • Clinical research coordination • Documentation and regulatory compliance • Data collection and reporting • Communication and coordination • Time management and multitasking • Analytical and problem-solving skills • Team collaboration About the Company • Tata Memorial Centre is India’s premier government cancer research and treatment institution known for its leadership in oncology care, epidemiology research and public health initiativesDate of Walk-in-Interview28-01-2026Official NotificationClick Here

Role & Responsibilities • Provide comprehensive medical care to OPD and IPD patients • Diagnose and manage acute and chronic medical conditions • Prescribe medications and treatment plans as per clinical guidelines • Handle emergency cases and provide basic and advanced life support • Conduct clinical examinations and interpret investigation reports • Maintain accurate patient records and medical documentation • Participate in community health programs and public health initiatives • Ensure compliance with government healthcare protocols Qualifications & Experience • MBBS / MD / MS from a recognized institution • Age limit: 18 – 38 years (5 years relaxation for reserved categories)Name of the PostsVacanciesEducationMedical Officer02MBBS, MD/MS Skills • Clinical diagnosis and patient assessment • Emergency care and life support • Medical documentation and reporting • Communication and patient counselling • Public health awareness • Team coordination and decision making About the Company • Zilla Parishad is a government body responsible for delivering public healthcare services in rural and semi-urban regions of Maharashtra through primary and community health centersApplication Closing date20-01-2026Official NotificationClick Here