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Role & Responsibilities • Receive customer complaints through calls, emails, and faxes • Ensure accurate capture and entry of complaint information • Own the complaint handling process, from assessment to closure • Assess complaints for potential Medical Device Reporting (MDR) and submit to the client • Follow up for additional information and product returns • Serve as the primary, single source of contact for customers • Gather event registration information as defined by SOPs • Manage events through registration, regulatory reporting, sample retrieval, investigation, and customer response • Collaborate with SMEs, QAs, and team leads to ensure complaint closure • Escalate significant events to the team lead in a timely manner • Comply with company policies and procedures, including information security management • Review and assess complaints processed by peers as part of a cross-utilization approach Qualification • Bachelor's of Science in Nursing or Pharmacy • Allied Medical Graduate (preferably with clinical experience) • Registered Nurse or Pharmacist preferred Experience • Experience in complaint handling and customer service • Clinical experience is an added advantage Skills • Ability to write effective medical and technical narratives for complaints • Good communication skills, both telephonic and written • Strong analytical and problem-solving skills • Proficient computer and keyboarding skills • Critical thinking skills to determine necessary questions for gathering information • Excellent customer service skills About the Company • Wipro Limited is a leading technology services and consulting company, focused on building innovative solutions that address clients’ most complex digital transformation needs. With a global presence, Wipro delivers solutions that help customers, colleagues, and communities thrive.
Role & Responsibilities • Perform medical monitoring of clinical trials, ensuring safety and efficacy data are managed in accordance with protocols • Lead safety oversight throughout the clinical study lifecycle, including evaluation and monitoring of adverse events (AEs) and serious adverse events (SAEs) • Review safety reports, including SAE narratives, CIOMS reports, MedWatch reports, and aggregate reports • Provide medical input during protocol development, ensuring safety aspects are covered • Advise study sponsors and teams on inclusion/exclusion criteria, eligibility, protocol design, and halting rules • Collaborate with Safety Monitors to implement safety management activities and achieve study objectives • Participate in safety oversight committees and consult with sponsors, investigators, and pharmaceutical partners • Engage in bid preparation, bid defense meetings, and other business development activities • Participate in regulatory meetings and provide medical consultancy services for various documents Qualification • MD, MBBS, MBBCh, or equivalent medical degree Experience • Minimum of 2 years of experience in clinical practice or pharmaceutical medicine (clinical research, pharmacovigilance, medical affairs, regulatory) • Experience in safety monitoring, medical review, and serious adverse event reporting preferred • Demonstrated expertise in clinical trial data collection and regulatory submissions Skills • Excellent clinical judgment and the ability to communicate complex clinical issues • Strong leadership and teamwork skills to foster a positive, cross-functional work environment • Ability to direct activities and provide creative solutions in a medical setting • Proficient in verbal and written communication skills About the Company • Emmes Group is a global leader in clinical research, dedicated to advancing medical discoveries with expertise in clinical trials, safety monitoring, and regulatory compliance.
Roles & Responsibilities • Develop, write, review, and finalize high-quality scientific publications including manuscripts, abstracts, posters, slide decks, and congress materials • Ensure scientific accuracy, data integrity, and strategic alignment across all publication deliverables • Collaborate with authors, clients, and internal stakeholders to ensure clarity, compliance, and impactful communication • Mentor and guide junior medical writers, providing constructive feedback and sharing best practices • Support development of digital scientific content such as infographics, summaries, and visual abstracts • Contribute to proposal writing, pitches, and new business development initiatives as required • Ensure adherence to publication ethics, authorship criteria, and industry guidelines Qualification • PhD / MD / PharmD / M.Pharm / M.Sc in Life Sciences or related discipline Experience • Minimum 4+ years of experience in scientific or medical writing with a strong focus on publications Skills • Excellent scientific writing, editing, and communication skills • Strong understanding of clinical trial data, literature evaluation, and data interpretation • Knowledge of publication standards and guidelines including GPP, ICMJE, and journal/congress requirements • Ability to manage multiple projects, meet deadlines, and work collaboratively with cross-functional teams About the Company VUEVERSE is a growing medical communications and scientific writing organization specializing in high-quality, compliant, and impactful publication solutions, supporting life sciences and healthcare clients across global markets.
Role & Responsibilities • Lead and implement clinical trial activities as Clinical Trial Lead for one or more trials • Manage interactions with local health authorities and Subject Expert Committees • Plan, execute, and oversee study startup, conduct, and close-out activities • Develop and review protocols, informed consent forms (ICFs), and clinical quality documents • Supervise clinical data generation and validation, including CRF design and query resolution • Contribute to clinical development planning and provide medical insights for future trials • Support risk management plans (RMPs) and conduct signal detection activities • Provide leadership and guidance to a team of supporting Clinical Scientists Qualification • Medical qualification (MD in Pharmacology, Oncology, or Hematology preferred) Experience • 10+ years of experience in clinical science or clinical research • Experience in leading scientific interactions with DCGI and Subject Expert Committees • Oncology and Hematology therapeutic areas experience preferred Skills • Strong understanding of GCP/ICH guidelines, drug development processes, and study design • Ability to analyze clinical data trends and support program-specific data review • Proficient communication, problem-solving, and critical thinking skills • Strong planning and project management skills, with an ability to work effectively under pressure • Proficient in Microsoft Word, Excel, PowerPoint, and data reporting tools (e.g., RAVE) About the Company • Bristol Myers Squibb is a global biopharmaceutical leader, committed to advancing patients' lives through innovative science and cutting-edge therapies in oncology, immunology, cardiovascular disease, and fibrosis.
Role & Responsibilities • Conduct medical review and approval of selected scientific and literature articles • Review Individual Case Safety Reports (ICSRs) in the safety database • Perform medical labeling, causality assessment, and seriousness evaluation • Follow up with reporters to obtain missing or additional safety information • Review aggregate safety reports, including Periodic Safety Update Reports (PSURs) and Periodic Adverse Drug Experience Reports (PADERs) • Provide medical and scientific conclusions for benefit–risk assessments • Review and support Risk Management Plans (RMPs) • Contribute to signal detection and signal management activities • Ensure compliance with global pharmacovigilance regulations Qualification • MBBS or MD in Pharmacology Experience • 0–1 year of experience in pharmacovigilance or drug safety Skills • Strong understanding of ICSR processing and safety databases • Knowledge of global PV regulations (ICH, GVP, FDA, EMA) is an advantage • Prior experience in a regulated pharmaceutical company is a plus About the Company • Emcure Pharmaceuticals is a leading Indian pharmaceutical company, offering expertise in pharmacovigilance and drug safety operations globally.
Role & Responsibilities • Engage scientifically with oncologists and key healthcare professionals (HCPs) • Deliver medical education and facilitate knowledge exchange • Support clinical research, Investigator Sponsored Studies (ISS), and real-world evidence generation • Ensure compliance with global medical standards and guidelines • Contribute to scientific exchange and evidence generation in oncology Qualification • MD (Pharmacology) – Freshers with strong academics and oncology exposure • For other Doctorate degrees: Medico marketing experience in Oncology is mandatory Experience • Oncology experience or relevant medico marketing background Skills • Strong scientific knowledge in oncology • Excellent communication and engagement skills with healthcare professionals • Ability to work in a cross-functional, global medical affairs team About the Company • Global Pharmaceutical MNC with a commitment to improving patient outcomes through cutting-edge oncology solutions and scientific leadership.
Role & Responsibilities • Engage scientifically with healthcare professionals and key external experts • Deliver evidence-based scientific discussions and presentations • Provide field insights to support Medical Affairs initiatives • Support advisory boards, medical meetings, and scientific events • Respond to medical information requests in a compliant manner Qualification • Degree in Medicine / Pharmacy (MD, PhD, PharmD preferred) Experience • Prior experience as MSL or in Medical Affairs preferred Skills • Strong scientific knowledge and understanding of therapeutic areas • Excellent communication and presentation skills • Ability to travel within Delhi and surrounding areas About the Company • IQVIA offering cutting-edge solutions in the healthcare and pharmaceutical industry, committed to driving scientific engagement and delivering impactful medical insights.
Role & Responsibilities • Manually validate the process of transforming data for research, ensuring data is optimised for storage and easily computable • Review patient notes in Electronic Health Records (EHR) when required • Collaborate with the AI team in developing high-quality software to interpret EHR data • Tag datasets with high-level accuracy for the development of artificial intelligence models Qualification • MBBS from a reputed medical institution in India Experience • Strong understanding of clinical medicine and patient care • Ability to review and understand scientific literature, including PubMed articles and medical journals Skills • Basic computer literacy and familiarity with office suites • Basic knowledge of prompt engineering for Large Language Models • Elementary knowledge of biostatistics (preferred) • Understanding of EHR data within the US healthcare system (preferred) • Prior experience working in a technology or corporate environment (preferred) About the Company • nference Labs Bangalore is the India hub of nference, a global leader in computational biomedicine. The team is at the forefront of building cutting-edge biomedical intelligence platforms and collaborates on groundbreaking biomedical AI initiatives.
Role & Responsibilities • Deliver high-quality patient care, collaborating with physicians and supporting medical treatments and procedures • Monitor patient progress and coordinate care with other healthcare professionals • Ensure compliance with medical protocols and guidelines • Educate patients and their families about medical conditions and treatment plans • Provide training and support to team members in the healthcare setting Qualification • MBBS or equivalent medical degree from a recognized institution • Registration with the Medical Council of India (MCI) Experience • Strong background in Medicine and Patient Care • Experience in surgery or assisting in surgical procedures Skills • Ability to work collaboratively with physicians and other medical professionals • Excellent communication and interpersonal skills • Strong problem-solving and decision-making abilities in healthcare settings About the Company • Tulasi Healthcare is a leading provider of mental health and rehabilitation services for psychiatric disorders and substance abuse. With over 20 years of expertise, it is the largest private mental health establishment in North India, providing integrated preventive and therapeutic solutions through clinics, rehabilitation centers, and online platforms.
Role & Responsibilities • Provide medical review, analysis, and guidance during the case handling and reporting cycle of Individual Case Safety Reports (ICSRs) and ADR reports for investigational and marketed products • Conduct detailed ICSR Medical Review to assess causality, seriousness, and completeness, ensuring compliance with regulatory requirements • Write safety sections of Aggregate Reports such as PSURs, CASRs, and PADERs, including benefit-risk assessments • Guide Drug Safety Associates on medical aspects of drug safety, including case assessments and aggregate analysis • Analyze ADRs during ongoing surveillance and signal detection • Participate in Safety Review Meetings and client discussions to provide medical insights and recommendations • Maintain personal readiness for internal audits or regulatory inspections Qualification • MBBS, MD in Pharmacology or equivalent Experience • Clinical research or pharmacovigilance experience • Strong understanding of ICSR processes and global safety regulations Skills • Analytical and problem-solving skills • Excellent verbal/written communication skills • Strong presentation skills • Client-focused approach to work • Excellent organizational and prioritization skills About the Company • Vizen Life Sciences Pvt Ltd is a leading company specializing in drug safety and pharmacovigilance, offering medical expertise to ensure regulatory compliance and the safety of investigational and marketed pharmaceutical products.
Role & Responsibilities • Deliver medical care under the supervision of Registrars and senior medical staff • Conduct patient interviews and examinations, identifying clinical issues as they arise • Arrange investigations, surgical treatment, medical treatment, and discharge as directed by the Registrar/Consultant • Participate in shift rosters, including on-call shifts • Work collaboratively within a multidisciplinary team and contribute to the department's clinical operations Qualification • Degree qualification from a recognized tertiary institution • Current registration or eligibility for registration as a Medical Practitioner with the Medical Board of Australia • Successful completion of Medical Internship Experience • Experience working in a clinical environment is desirable, preferably in neurosurgery or related specialties Skills • Strong clinical assessment and diagnostic skills • Ability to work effectively under pressure and in a fast-paced environment • Excellent communication and interpersonal skillsBenefits • 4 to 6 weeks annual leave with 14%-17.5% loading • 12.75% employer contribution to superannuation • Professional development assistance (allowance, PD leave, and exam leave) • Attractive salary packaging options About the Company • Townsville Hospital and Health Service offers a dynamic clinical environment with access to advanced medical practice and research. As a leading tertiary and referral service, we support professional growth through complex casework, mentorship, and structured training pathways.
Role & Responsibilities • Provide comprehensive medical care to inpatients across various specialties, including orthopaedic, oncology, cardiac, neurology, neurosurgery, urology, general surgical, general medical, and paediatric care • Liaise directly with treating specialists and other medical officers to ensure high-quality patient care • Work in a 550-bed acute hospital with a focus on improving patient health outcomes and experience • Gain experience in a diverse range of medical specialties while working closely with experienced specialists and healthcare teams • Work 5 shifts per fortnight, including day and night shifts (12.5-hour shifts) with a focus on effective handovers at the end of each shift Qualification • AMC-recognized Australian medical degree or completion of both parts of the Australian Medical Council exams • Current general registration with AHPRA Experience • Minimum 2 years of experience in an Australian hospital system as an AHPRA-registered doctor • PGY3 or greater (or currently completing PGY2) Skills • Advanced communication skills with a caring and respectful approach to patient care • Ability to work effectively in a team and demonstrate accountability, excellence, and integrity • Passionate about patient-centered care and safety About the Company • Epworth HealthCare is Victoria’s largest not-for-profit private healthcare group, renowned for excellence in diagnosis, treatment, care, and rehabilitation. The organization embraces the latest in evidence-based medicine to pioneer treatments and services for patients.
Role & Responsibilities • Interview, examine, and assess patients presenting to the hospital • Document clinical care and patient progress • Contribute to after-hours cover for the hospital • Actively participate in patient safety initiatives and reporting clinical incidents • Maintain continuous clinical care of patients Qualification • Medical degree (MBBS or equivalent) Experience • Experience in clinical care and patient assessments • Prior experience in a hospital or healthcare setting preferred Skills • Strong clinical, diagnostic, and communication skills • Ability to work independently and in a team environment • Commitment to patient safety and quality care • Understanding of cultural safety and equity in healthcare, especially with Aboriginal and Torres Strait Islander communities About the Company • Metro North Hospital & Health Service is a dynamic, world-class health service embracing technology and innovation, committed to providing excellent healthcare, quality teaching, and cutting-edge research.
Role & Responsibilities • Diagnose and treat common medical conditions for adult and pediatric patients • Conduct physical examinations and assess patient medical histories • Prescribe medications and treatment plans in line with DHA/DOH guidelines • Provide preventive care, health education, and lifestyle counseling • Refer patients to specialists when required • Maintain accurate and confidential medical records • Ensure compliance with UAE healthcare regulations and clinic policies Qualification • MBBS or equivalent medical degree Experience • 2 - 7 years of experience as a General Practitioner Skills • Fluent in Hindi (mandatory) • Good communication skills in English • Strong clinical and diagnostic skills • Ability to work independently and as part of a medical team About the Company • Talentgrade HR is a recruitment agency that connects healthcare professionals with leading employers in the UAE, focusing on delivering high-quality healthcare services.
Role & Responsibilities • Conduct consultations and provide diagnosis, treatment, and management for patients with hematologic or oncologic diseases • Order and interpret diagnostic tests (CBCs, bone marrow biopsies, imaging, pathology reports, biomarkers) • Develop individualized treatment plans (chemotherapy, immunotherapy, targeted therapy, radiation, transplant, supportive care) • Administer and monitor cancer treatments and blood disorder therapies • Provide inpatient and outpatient care • Coordinate multidisciplinary care with surgeons, radiologists, pathologists, and other specialists • Counsel patients and families regarding diagnosis, prognosis, and treatment options • Participate in tumor boards and clinical review meetings • Maintain accurate medical records and documentation • Support or participate in clinical research and trials where applicable • Stay updated with advancements in oncology and hematology Qualification • Doctor of Surgery (MS) in Oncology or equivalent Experience • 6 - 12 years of experience in hematology and oncology • Expertise in chemotherapy and managing complex patient care Skills • Board certification or unencumbered license/registration from home country • Completion of Internal Medicine with a Fellowship in Hematology/Oncology • Excellent communication skills and proficiency in English • Ability to work in a multicultural team and manage long-term patient care About the Company • TreeTopHealth Pvt Limited is a healthcare provider offering advanced medical services with a focus on oncology and hematology care, delivering comprehensive treatment options to patients.
Role & Responsibilities • Provide general surgery care, including diagnosis, surgical procedures, and post-operative care • Perform surgeries as per established medical standards and protocols • Ensure patient safety and proper preparation for surgery • Collaborate with medical teams to deliver comprehensive surgical care • Maintain accurate medical records and ensure compliance with health regulations Qualification • Doctor of Surgery (MS) in General Surgery Experience • 4 - 9 years of experience in general surgery • Minimum of 5 years of post-residency experience in general surgery with a proven track record of successful surgical outcomes Skills • Board certification or board eligibility in General Surgery from a recognized medical board • Strong surgical skills with attention to patient care • Ability to work in a collaborative, fast-paced environment About the Company • DM Healthcare LLC is a prominent healthcare provider in Oman, offering a range of medical services with a focus on quality and patient care.
Role & Responsibilities • Provide medical care in an industrial clinic and on-site work environment • Strong knowledge of PDO and international occupational health standards • Identify work-related health conditions and guide follow-up • Classify occupational injuries and illnesses • Interpret drug and alcohol screening results • Conduct fitness-to-work assessments for Oil & Gas personnel Qualification • MBBS (Medicine) Experience • 4 - 9 years of experience, with at least 3 years in Occupational Health Skills • In-depth knowledge of occupational health standards and practices • Strong diagnostic and decision-making skills • Ability to manage workplace health assessments and screenings About the Company • Aster DM Healthcare is a leading healthcare provider in the Middle East, committed to providing world-class medical services across various specialties.
Roles & Responsibilities • Manage clinical study documents in line with client, regulatory, and ICON requirements • Perform document receipt, review, quality checks, scanning, indexing, filing, and archiving in the Trial Master File (TMF) • Ensure continuous compliance with ICON SOPs, work procedures, and applicable regulatory guidelines • Collaborate with study teams, clients, and internal ICON departments to support study deliverables • Participate in internal and external audits and support inspection readiness activities • Prepare and maintain TMF status reports and tracking logs • Identify gaps or issues in TMF documentation and support corrective actions • Participate in training programs to enhance TMF and clinical research knowledge • Support special projects and additional responsibilities as assigned by the Manager Qualification • B.Pharm / M.Pharm / Pharm.D / BSc / MSc in Life Sciences or related disciplines Experience • 1-15 years of experience in TMF management or clinical document management • Strong understanding of clinical trial documentation and TMF processes Skills • Strong oral and written communication skills • Excellent attention to detail and document accuracy • Good interpersonal and stakeholder coordination skills • Strong organizational and time management abilities • Working knowledge of clinical trial regulations and documentation standards About the Company ICON plc is a global leader in clinical research and healthcare intelligence, committed to advancing clinical development through innovation, partnership, and integrity, while fostering an inclusive work environment focused on improving patient lives worldwide.
Role & Responsibilities • Provide medical services and ensure the safety and well-being of employees • Conduct medical assessments, check-ups, and handle medical emergencies • Maintain health records and ensure compliance with safety regulations • Manage the implementation of health programs and initiatives Qualification Name of the PostsVacanciesEducationMedical Officer02MBBS Experience • Experience in a medical or healthcare environment is preferred Skills • Strong communication and interpersonal skills • Ability to work under pressure and manage medical emergencies • Knowledge of health and safety regulationsAge Limit • Minimum Age: 21 Years • Maximum Age: 45 Years • Age relaxation based on the organization's norms Selection Process • Interview Application Fee • No application feeAddress • Saturday Club, SAIL Officers Colony, • SAIL Collieries Division, • Chasnalla, Dhanbad, Jharkhand – 828135 About the Company • Steel Authority of India Limited (SAIL) is one of the largest steel manufacturing companies in India, committed to producing high-quality steel products.Application Closing date30-01-2026Official Notification and Application FormClick Here
Role & Responsibilities • Provide ongoing medical monitoring for assigned clinical trials • Conduct real-time safety review of AEs and SAEs to ensure participant safety • Evaluate safety signals, trends, laboratory and ECG abnormalities • Contribute to protocol development, amendments and review of IBs, CSRs and SAPs • Support preparation and review of safety narratives, DSURs and periodic safety reports • Collaborate with pharmacovigilance teams for safety data management and regulatory responses • Participate in Steering Committees and Data Safety Monitoring Boards (DSMBs) • Provide medical expertise during site initiation, monitoring visits, audits and inspections • Review inclusion/exclusion criteria for complex cases and manage protocol deviations with CAPA • Ensure compliance with ICH-GCP, regulatory and ethical guidelines • Support regulatory submissions and inspection readiness activities • Deliver medical training to internal teams and site staff • Work cross-functionally with clinical operations, data management, biostatistics and project teams Qualifications • MD or equivalent medical degree (specialty training preferred)Experience • 3–7 years of clinical research experience in pharma, biotech or CRO • Prior experience as Medical Monitor / Safety Physician preferred • Strong understanding of ICH-GCP, FDA, EMA and CDSCO regulatory requirements • In-depth knowledge of clinical trial methodology and drug development lifecycle Skills • Medical monitoring and safety signal evaluation • Protocol development and regulatory documentation • Pharmacovigilance and safety reporting • Clinical trial compliance and audit readiness • Cross-functional collaboration and stakeholder management • Scientific writing and medical training delivery About the Company • Micro Crispr Pvt. Ltd. is a biotechnology-driven organization focused on innovative research and clinical development solutions, supporting advanced clinical programs through strong scientific, regulatory and ethical standards