Hyderabad Healthcare Jobs

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.

Roles & Responsibilities • Approve and schedule Individual Case Safety Reports (ICSRs) in the Argus database for submission to Health Authorities • Submit safety cases to Health Authorities, Business Partners, and Affiliates as per regulatory requirements • Ensure strict adherence to internal and external timelines to maintain regulatory compliance • Schedule and approve regulatory reports based on defined reporting obligations • Perform quality review of ICSRs to ensure accuracy, completeness, and compliance with PV guidelines • Support regulatory submission activities and maintain high-quality pharmacovigilance standards Qualification • B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy)Experience • 4 to 6 years of relevant Pharmacovigilance experience • Mandatory hands-on experience in ICSR Quality Review and Regulatory Submissions • Strong working experience with the Argus Safety Database Skills • Strong knowledge of global Pharmacovigilance regulations and reporting guidelines • Expertise in ICSR quality review, compliance, and regulatory submissions • High attention to detail with strong analytical skills • Excellent communication, coordination, and time management abilities About the Company Vizen Life Sciences is a growing life sciences organization focused on delivering high-quality pharmacovigilance, regulatory, and safety solutions, supporting global healthcare and regulatory compliance standards.

Roles & Responsibilities• Assess, diagnose, and treat patients with physical injuries, movement disorders, or functional limitations• Develop and implement individualized physiotherapy and rehabilitation programs• Provide manual therapy, exercise therapy, and electrotherapy based on patient needs• Educate patients and family members on recovery plans, posture correction, and preventive care• Monitor patient progress and modify treatment plans accordingly• Maintain accurate clinical documentation and patient treatment records• Collaborate with doctors, nurses, and allied healthcare professionals for integrated patient care• Ensure adherence to hospital quality standards, safety protocols, and infection control guidelinesQualifications• Bachelor’s or Master’s degree in Physiotherapy (BPT / MPT) from a recognized institution• Valid physiotherapy registrationExperience• 2–3 years of clinical physiotherapy experience preferredSkills• Strong clinical assessment and rehabilitation skills• Manual therapy and therapeutic exercise expertise• Knowledge of electrotherapy modalities• Excellent communication and interpersonal skills• Patient-centric and empathetic approach• Ability to work effectively within a multidisciplinary healthcare teamAdditional Requirements• Male candidates preferred• Willingness to work any 8-hour shift between 8:00 AM and 8:00 PMBenefits• Paid sick leave• Provident FundAbout the CompanyZoi Hospitals is a growing healthcare organization committed to delivering high-quality, patient-centered medical services. With a focus on clinical excellence, safety, and compassionate care, Zoi Hospitals provides a supportive environment for healthcare professionals to grow while making a meaningful impact on patient recovery and overall well-being.

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

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 • 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 • 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

Roles & Responsibilities: • Dispense veterinary medicines accurately as per veterinarian prescriptions • Explain dosage, usage instructions, and precautions to pet parents when required • Ensure proper labeling, packaging, and documentation of medicines • Manage pharmacy inventory, stock levels, and expiry monitoring • Coordinate with purchase/inventory teams for timely replenishment • Ensure proper storage conditions for medicines and vaccines • Maintain pharmacy records, prescriptions, and controlled drug registers • Support audits, stock reconciliation, and monthly reporting • Maintain hygiene and cleanliness of the pharmacy area • Assist veterinarians and technicians by ensuring medicine availability • Follow SOPs, safety guidelines, and regulatory requirements • Provide courteous service and effective communication with customers and staff Qualifications: • D.Pharm or B.Pharm from a recognized institute • Valid Pharmacist License (Telangana – mandatory) Experience: • Experience in medical or veterinary pharmacy preferred Skills: • Good communication and customer service skills • Knowledge of veterinary medicines (added advantage) • Inventory management and basic computer proficiency About the Company: Crown Veterinary Services Pvt. Ltd. is a professionally managed veterinary healthcare organization providing high-quality clinical and pharmacy services. The company is committed to animal welfare, ethical practices, and delivering reliable veterinary care supported by trained professionals and standardized operating procedures.

Role & Responsibilities:• Assess, plan, and deliver physiotherapy services for children with developmental delays and challenges• Conduct detailed sensory-motor and functional skill assessments• Identify developmental delays, sensory processing issues, and motor skill deficits• Develop individualized therapy plans with measurable goals and expected outcomes• Deliver child-centric therapy sessions focusing on sensory integration, fine motor and gross motor skills, balance, coordination, ADLs, postural control, and muscle tone management• Adapt therapy techniques based on each child’s needs, response, and progress• Monitor, track, and document session-wise progress toward therapy goals• Educate and guide parents on home-based programs, sensory diets, and daily activity strategies• Conduct parent meetings to explain progress, challenges, and next steps• Train parents and caregivers to support sensory regulation and motor skill development at home• Collaborate with an interdisciplinary team including speech therapists, behavior therapists, and special educators• Participate in case discussions, goal reviews, and coordinated care planning• Maintain accurate and timely documentation including assessments, session notes, and progress reportsQualification:• Bachelor’s Degree in Physiotherapy (BPT)Experience:• Experience in pediatric physiotherapy preferred• Freshers with strong interest in pediatric rehabilitation may also applySkills Required:• Strong knowledge of pediatric physiology and anatomy• Understanding of developmental milestones and pediatric conditions• Pediatric assessment and therapy planning skills• Medical terminology and documentation skills• Parent counseling and communication skills• Ability to work collaboratively within a multidisciplinary teamAbout the Company:Rising Sun Child Development Center is a multidisciplinary pediatric therapy center dedicated to supporting children with developmental, sensory, and motor challenges. The center follows a holistic and child-focused approach by integrating physiotherapy, speech therapy, behavioral therapy, and special education to help children achieve functional independence and age-appropriate developmental milestones in a nurturing and structured environment.

Roles & Responsibilities: • Enter, update, and maintain accurate data in the Pharma CRM system • Support CRM operations for pharmaceutical and clinical research projects • Coordinate with internal teams to ensure timely and accurate data availability • Perform routine data validation, verification, and quality checks • Assist in preparation of basic CRM, MIS, and operational reports • Adhere to SOPs, data confidentiality norms, and compliance guidelines Qualification: • Any Graduate Experience: • Freshers / 0-1 year of experience Skills: • Minimum typing speed of 20 WPM • Basic knowledge of MS Word and MS Excel • Good attention to detail and data accuracy • Willingness to learn Pharma CRM and shared services processes • Clear written and verbal communication skills • Ability to work in a team-oriented, process-driven environment About the Company: Vimta Labs Limited is a leading contract research and testing organization in India, providing services across pharmaceuticals, clinical research, food, environment, and healthcare. Known for its strong regulatory compliance and quality-driven approach, Vimta offers an excellent platform for fresh graduates to gain hands-on exposure to regulated pharma operations and build long-term careers in the life sciences industry.

Roles & Responsibilities: • Prepare summary reports for medical devices • Perform trend analysis on customer complaints and product performance • Conduct monthly and ad-hoc data analysis from complaints, sales, and trending databases • Carry out literature searches and review clinical, scientific, and medical references • Identify, interpret, and evaluate data from medical literature, clinical studies, and post-market sources • Compile and submit clinical and post-market surveillance (PMS) documents • Support international regulatory submissions in line with global medical device regulations • Contribute to PMS plans and safety reports for assigned device portfolios Qualification: • Relevant degree in Life Sciences, Biomedical Engineering, Pharmacy (B.Pharm, D.Pharm, M.Pharm) , or related discipline Experience: • 3-6 years of experience in Medical Devices domain • Hands-on experience in medical review and post-market surveillance Skills: • Strong knowledge of medical device regulations and PMS requirements • Experience in complaint trending and safety data analysis • Expertise in literature search and regulatory documentation • Excellent analytical, documentation, and communication skills • Ability to work in a fast-paced, office-based environment • Immediate joiners preferred About the Company: ANRI Solutions is a leading recruitment partner connecting skilled professionals with top pharmaceutical, medical device, and healthcare organizations across India and globally.

Roles & Responsibilities: • Assist in execution of clinical trials as per protocol and SOPs • Support subject screening, registration, and study documentation • Maintain clinical trial data, logs, and regulatory records • Ensure compliance with ICH-GCP and internal quality standards • Support quality management, medical writing, or sample collection activities (role-dependent)Qualification: • B.Sc • Bachelor of Pharmacy (B.Pharm) • Master of Pharmacy (M.Pharm) • B.Sc Nursing / GNM • Diploma in Medical Laboratory Technology (DMLT) Experience: • 0–3 years • Freshers with relevant academic exposure can applySkills: • Basic knowledge of clinical research processes • Good documentation and communication skills • Willingness to learn and work in a CRO environment • Attention to detail and compliance orientation Walk-in Details:Walk-in Date: 21 January 2026 Interview Mode: Face-to-FaceSelection Process: HR InterviewAbout the Company: Aizant Drug Research Solutions is a reputed Clinical Research Organization (CRO) providing end-to-end services in clinical trials, pharmacovigilance, medical writing, and quality management, supporting global pharmaceutical and biotech companies.

Roles & Responsibilities: • Execute centralized activities for global clinical trials • Coordinate with CROs, Country Trial Managers, CTMs, CRAs, and study teams • Manage essential documents, ethics committee submissions, and regulatory files • Support study start-up activities including site activation and documentation • Review and maintain clinical systems such as CTMS, eTMF, and Veeva Vault • Oversee outsourcing, contracting, translation, and investigator file setup • Ensure quality control and compliance with ICH-GCP and internal standards • Act as primary point of contact for centralized trial start-up and maintenance activities Qualification: • Bachelor’s degree in Life Sciences, Legal, or Business Administration • Advanced degree preferred Experience: • 3+ years of experience in clinical development or clinical operations • Experience in pharma, biotech, or CRO environments • Hands-on experience in IRB / IEC submissions and site activation Skills: • Strong knowledge of ICH-GCP and global regulatory documentation • Proficiency in CTMS, eTMF, Veeva Vault, MS Office, and SharePoint • Excellent organizational, communication, and coordination skills • Strong attention to detail and decision-making ability • Therapeutic area exposure (Oncology, Cardiology, Immunology) is a plus About the Company: Bristol Myers Squibb is a leading global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines that transform patients’ lives through science.

Roles & Responsibilities: • Dispense and compound medications as per physician prescriptions • Suggest OTC medicines and provide suitable alternatives when brands are unavailable • Counsel customers on dosage, usage, and general healthcare advice • Conduct basic health and wellness screenings • Ensure accurate billing, invoicing, and customer satisfaction • Receive stock and verify quantity, batch number, and expiry details • Manage inventory including short-expiry and non-moving medicines • Perform regular physical stock verification with system data • Maintain statutory registers and records as per applicable laws Qualification: For Pharmacist: • D.Pharm / B.Pharm / M.Pharm  For Pharmacist Assistant: • Minimum 12th Pass / Any GraduateExperience: • Freshers and experienced candidates can apply Skills: • Good knowledge of medicines and pharmaceutical products • Customer-focused attitude with strong interpersonal skills • Basic computer and billing skills • Attention to detail and inventory management skills Additional Information: • Accommodation provided by the company for male candidates. About the Company: Alliance Pharmacy is a growing healthcare brand committed to improving community health through accessible, reliable, and professional pharmacy services. We provide a supportive work environment with opportunities for learning, growth, and meaningful contribution to patient care.

Role & Responsibilities: • Prepare, compile, and submit regulatory dossiers for pharmaceutical export registrations to global regulatory authorities • Maintain CTD/eCTD documentation for product registrations, renewals, variations, and post-approval changes • Ensure compliance with international regulatory requirements and current guidelines across export markets • Act as a liaison with regulatory agencies, export authorities, and external consultants for submission queries and follow-ups • Coordinate with internal teams including QA, QC, Production, R&D, and Supply Chain to collect required technical documentation • Track submission timelines, monitor status, and respond to deficiency letters within defined timelines • Maintain organized regulatory databases, files, and documentation as per regulatory and company standards • Provide regulatory intelligence on evolving global regulations impacting pharmaceutical exports • Support labeling, packaging, and artwork compliance as per importing country requirements Qualification: • Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, or a related discipline Experience: • 1-4+ years of experience in pharmaceutical regulatory affairs • Preferable exposure to export regulatory submissions and international markets Skills: • Strong knowledge of global regulatory frameworks and export documentation requirements • Hands-on experience with CTD/eCTD dossier preparation and submission tracking • Familiarity with electronic submission systems and regulatory agency portals • Excellent communication, coordination, and stakeholder management skills • Strong organizational ability and attention to detail • Good command of written and spoken English About the Company: The organization operates within the pharmaceutical sector, supporting global product registrations and export compliance across multiple international markets. It emphasizes regulatory excellence, cross-functional collaboration, and adherence to global quality and compliance standards to ensure timely product approvals and sustainable business growth.

Role & Responsibilities: • Dispense prescription medications accurately and efficiently in accordance with prescriptions and standard operating procedures • Review prescriptions for appropriateness, dosage accuracy, and potential drug interactions • Maintain accurate and up-to-date patient medication profiles and pharmacy records • Oversee inventory management including stock monitoring, ordering, storage, and expiry control • Ensure compliance with applicable pharmacy laws, regulations, quality standards, and company policies • Maintain statistical, operational, and financial pharmacy records • Support safe medication practices and ensure patient safety at all times • Provide clear medication counseling and respond to patient queries professionally • Coordinate with internal teams to ensure smooth pharmacy operations • Work effectively in a fast-paced environment while managing multiple tasks • Be flexible to work in shifts as per business requirements Qualification: • Bachelor of Pharmacy (B.Pharm) / Master of Pharmacy (M.Pharm) / Pharm.D from a recognized institution • Active and valid Pharmacy license in Telangana – mandatory Experience: • Freshers or candidates with relevant pharmacy experience are welcome • Experience in hospital, retail, or healthcare service environments is an advantage Skills: • Strong knowledge of pharmaceuticals, pharmacology, and pharmacy operations • Excellent attention to detail and accuracy • Good communication and interpersonal skills • Ability to multitask and work efficiently under pressure • Customer-focused approach with commitment to quality service • Basic computer and record-keeping skills About the Company: Saince HealthTech (SHT) is the India subsidiary of Saince Inc., USA, an award-winning healthcare solutions provider with a 95% customer satisfaction rating among hospitals and physicians. Headquartered in Hyderabad, SHT supports healthcare organizations across the United States and has been recognized as one of the fastest-growing private companies in the nation. The company is committed to innovation, quality, and excellence in healthcare delivery while offering a supportive and growth-oriented work environment.

Role & Responsibilities • Perform medical review of Individual Case Safety Reports (ICSRs) • Ensure medical accuracy, completeness, and regulatory compliance of safety cases • Apply clinical judgment for case assessment, seriousness, causality, and expectedness • Support global pharmacovigilance and regulatory reporting activities • Ensure adherence to GVP, ICH guidelines, and internal SOPs Qualifications & Experience • MBBS / MD with valid MCI registration • Minimum 1 year of hands-on experience in ICSR medical review Skills • Strong knowledge of pharmacovigilance and clinical terminology • Understanding of regulatory reporting requirements • Good analytical and documentation skills About the Company • Indegene is a global life sciences solutions provider delivering pharmacovigilance, medical affairs, and regulatory services across worldwide markets