Pharma, Clinical Research & Healthcare Jobs in India
511 open roles from pharma companies, CROs and hospitals, with new openings added most days. Apply directly through each employer's own page or contact.
Showing 151–175 of 429 jobs
- B
Clinical Trial Support Specialist
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite30 SeptSupport end-to-end clinical trial submission operations by preparing submission-ready documents, maintaining clinical trial systems and data, coordinating regulatory milestones, and enabling efficient clinical development activities across the oncology portfolio.
Medical Writer I / Medical Writer II
Parexel
Bangalore2-5 Years · Hybrid30 SeptDevelop high-quality pharmacovigilance and regulatory safety documents, conduct signal detection and assessment, synthesize scientific evidence, and support regulatory compliance across the product lifecycle.
Patient Reimbursement Coordinator - India
Syneos Health
Remote0-2 Years · Remote30 SeptCoordinate patient travel and reimbursement services for clinical trial participants, ensuring timely support, accurate processing, confidentiality, GCP compliance, and adherence to study-specific policies.
Therapy Business Manager – Neurolife (CNS Sales)
Abbott
Durg0-2 Years · Onsite29 SeptAbbott's Established Pharmaceuticals Division (EPD) is expanding its Neurolife franchise across Chhattisgarh, and the Therapy Business Manager role in Durg sits at the front line of that growth. Neurolife covers Abbott's central nervous system portfolio — products prescribed for epilepsy, neuropathic pain, migraine prophylaxis and mood disorders — making the territory manager the critical link between brand strategy and real-world patient outcomes. This is a high-ownership field position: you manage an independent territory, own prescription-generation targets, and shape how neurologists and psychiatrists in the region perceive Abbott's brands. For candidates with 2+ years in pharmaceutical selling, it offers MNC-grade training, structured career ladders, competitive incentives and exposure to one of India's fastest-growing specialty therapy areas.
Therapy Business Manager – Gastroenterology (GI Optima)
Abbott
Varanasi0-2 Years · Onsite29 SeptTherapy Business Manager – GI Optima is Abbott's frontline commercial leadership role within its Established Pharmaceuticals Division (EPD), responsible for driving prescription growth for the gastroenterology portfolio across the Varanasi territory. Abbott EPD's GI franchise — spanning digestive health, acid-peptic disorders and gut-health-oriented therapies — competes in one of India's fastest-growing chronic-prescription segments, making this position a direct lever on the division's market-share ambitions across Uttar Pradesh. The role blends science-led detailing with territory economics: the incumbent owns call averages, coverage and frequency norms while building durable relationships with gastroenterologists, consulting physicians, chemists and stockists. For ambitious pharmaceutical sales professionals, this is an excellent entry into a global MNC with structured training, ethical-promotion governance and a transparent pathway into area and regional business leadership.
Specialist, Quality Services – Product Complaints
Sanofi
Hyderabad2-5 Years · Onsite29 SeptSanofi's Global Manufacturing & Supply Services hub in Hyderabad is the operational backbone of the company's worldwide product quality agenda, and this Specialist Quality Services (Product Complaints) position sits at the frontline of post-market surveillance. The role owns intake, triage, categorization and closure of Product Technical Complaints across medical devices, pharmaceuticals, biologics and combination products — a workflow that directly protects patient safety and feeds the investigation, field alert and pharmacovigilance machinery of a 110,000-person life-sciences leader. Because Sanofi is investing heavily in AI-driven data standards and reusable quality data, specialists here gain exposure to modern QMS tooling and global cross-functional stakeholders. For an early-career quality professional, it is an exceptional launchpad: high regulatory visibility, structured GxP discipline and a clear route into broader quality, compliance and pharmacovigilance careers.
Associate Director, Real World Data Statistics
AstraZeneca
Bengaluru5+ Years · Hybrid29 SeptAlexion, AstraZeneca's rare disease unit, is expanding its epidemiology and real-world evidence capability in Bangalore with an Associate Director I/II, Real World Data Statistics. This individual-contributor leadership role sits at the intersection of advanced biostatistics and regulatory science, converting disease registry, natural history, EMR and claims data into evidence robust enough to withstand FDA, EMA and other health authority scrutiny. The position matters because rare disease programmes depend on external data to characterise small, dispersed patient populations, support label expansions and satisfy post-market commitments. For an experienced statistician it offers unusual scope: methodological innovation in missingness, linkage and confounding control, direct exposure to health authority interactions, and mentorship of a growing RWD statistics function within a biotech-paced, patient-centred environment backed by AstraZeneca's global scale.
Clinical Programmer I / II
AstraZeneca
Bengaluru2-5 Years · Hybrid29 SeptThe Clinical Programmer I/II role at AstraZeneca's Manyata Tech Park campus in Bangalore sits at the intersection of clinical science and software engineering — the precise place where modern drug development is being reinvented. Reporting into the Biometrics and Clinical Programming function, this individual-contributor position converts raw trial data from EDC and third-party vendors into validated datasets, automated quality checks and executive-ready dashboards that study teams use to spot anomalies weeks earlier. Because AstraZeneca's pipeline spans oncology, cardiovascular, respiratory and rare disease, the programmer's output directly shapes how quickly and confidently go/no-go decisions are made. For a technically strong SAS or Python developer who wants their code to carry patient-level consequence rather than purely commercial consequence, this is a rare hybrid of engineering craft, regulatory rigour and genuine therapeutic impact.
Associate Manager - Quality Investigations
Pfizer
Vizag5+ Years · Onsite29 SeptPfizer’s Vizag manufacturing site is a critical node in the company’s global supply chain, producing medicines that reach patients worldwide. The Associate Manager – Investigation role sits at the heart of quality assurance and compliance, ensuring that deviations, out-of-specification results, and atypical events are thoroughly examined and resolved. This position directly supports Pfizer’s quality culture, which is science- and risk-based, flexible, and patient-focused. By identifying root causes and implementing robust corrective and preventive actions, the incumbent protects product safety, regulatory standing, and supply continuity. For professionals with a pharma quality background, this is a compelling opportunity to work with a global leader, gain exposure to complex investigations, and develop expertise that is highly valued across the industry. The role offers visibility with cross-functional teams and regulatory inspections.
Associate Manager - Reliability Engineering
Pfizer
Visakhapatnam5+ Years · Onsite29 SeptPfizer’s Vizag manufacturing site is a critical node in the company’s global sterile injectables and pharmaceutical supply network. The Associate Manager – Reliability Engineering plays a central role in safeguarding asset uptime, calibration compliance, and cGMP readiness across utilities, buildings, and production equipment. This position is not just maintenance—it is a strategic enabler of uninterrupted medicine supply. By driving reliability-centered maintenance, root cause failure analysis, and predictive maintenance optimization, the role directly supports Pfizer’s mission to deliver breakthroughs to patients. For experienced engineering professionals, this is a compelling opportunity to work at the intersection of advanced manufacturing, quality systems, and regulatory compliance, with exposure to aseptic processing and process automation. Career growth is strong, and the impact on patient outcomes is tangible.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptDrive global regulatory intelligence surveillance and analysis across human and veterinary medicines, translating changing health authority requirements into actionable insights that support compliance, risk management, and Lonza's global CDMO operations.
District Manager - Neuroscience - Kolkata
Johnson & Johnson
Kolkata5+ Years · Onsite29 SeptDistrict Manager responsible for pharmaceutical sales growth across an assigned neuroscience territory, with a focus on psychiatry, healthcare-professional engagement, KOL development, distributor management and execution of scientific and commercial strategies.
Manager, Scientific Communications
Amgen
Hyderabad5+ Years · Onsite29 SeptManager-level Scientific Communications role within Amgen's Global Medical Organization, responsible for developing scientific and medical content, publications, medical information materials, and communication strategies across global audiences and therapeutic areas.
Clinical Project Manager - FSP
Thermo Fisher Scientific
Mumbai5+ Years · Remote29 SeptClinical Project Manager responsible for end-to-end delivery of clinical research projects, serving as the primary sponsor contact and leading cross-functional teams across quality, time, cost, risk, financial stewardship, and vendor oversight.
- B
Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite29 SeptScientific Writer II responsible for authoring and coordinating regulatory and clinical documents, integrating scientific, medical, and regulatory input while managing document strategy, review cycles, timelines, quality, and compliance.
Regulatory Intelligence Senior Specialist
Lonza
Hyderabad5+ Years · Hybrid29 SeptRegulatory Intelligence Senior Specialist responsible for global regulatory surveillance, impact assessment, regulatory trend analysis, stakeholder collaboration, intelligence reporting, dashboards, and regulatory risk identification across human and veterinary medicines.
Manager, Clinical Operations
Parexel
Bangalore5+ Years · Onsite29 SeptManager, Clinical Operations responsible for team oversight, clinical project delivery, resource planning, staff development, quality control, client management, and compliance with clinical research standards and regulations.
Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid29 SeptLead clinical operations teams at Syneos Health in Hyderabad, overseeing site activations, monitoring, and regulatory submissions.
Medical Science Liaison
Bayer
Delhi NCR2-5 Years · Hybrid29 SeptDrive scientific engagement and education as a Medical Science Liaison with Bayer in Delhi.
Quality Specialist (QMS, Documentation)
Merck KGaA
Bangalore5+ Years · Onsite29 SeptQuality Assurance Specialist responsible for managing QMS, quality documentation, audits, investigations, compliance, and continuous improvement within Merck's Life Science division in India.
Regional Manager, IC
Boston Scientific
Chandigarh5+ Years · Onsite29 SeptDrive interventional cardiology sales and lead regional teams at Boston Scientific in Chandigarh and New Delhi.
Principal Clinical Programmer (Rave EDC)
Syneos Health
Remote5+ Years · Remote29 SeptSenior clinical programming leadership role focused on Rave EDC programming, custom functions, clinical database development, technical support, study oversight, quality review, and program-level leadership across multiple clinical studies.
Clinical Monitoring (CM)
Syneos Health
Hyderabad2-5 Years · Hybrid29 SeptSupport clinical trial oversight through independent monitoring, patient-level data review, study and site-level trend analysis, risk identification, and risk-based quality management.
Expert Scientific Writer
Sanofi
Hyderabad5+ Years · Onsite28 SeptSanofi Business Operations in Hyderabad is seeking an Expert Scientific Writer to drive high-impact medical and publication content for Specialty Care, Vaccines, General Medicines and R&D portfolios. This role is central to Sanofi's global scientific communication strategy, ensuring accurate, compliant and compelling publication materials that inform healthcare professionals and support product lifecycle decisions. The writer will manage end-to-end development of abstracts, posters, manuscripts, slide decks and medical education assets in PromoMats/iEnvision, while coaching junior writers and partnering with medical, HEVA and commercial teams. For an experienced medical writing professional, this is a rare opportunity to shape therapeutic-area narratives, maintain Good Publication Practice standards and influence how Sanofi's clinical evidence reaches global stakeholders.
Senior Statistical Programmer
AstraZeneca
Bengaluru2-5 Years · Hybrid28 SeptBased at AstraZeneca's Manyata Tech Park campus in Bangalore, the Senior Statistical Programmer I role sits within the Oncology Biometrics Programming department—a critical function that turns raw clinical trial data into regulatory-ready evidence. As part of a global team dedicated to eliminating cancer as a cause of death, you will support and lead statistical programming activities across high-priority oncology studies, from clinical study report development to regulatory submissions and commercialisation. This is a compelling opportunity for an experienced SAS programmer who wants to see their code influence filings, accelerate patient access, and shape evidence-based decisions. AstraZeneca's deep pipeline, collaborative research culture, and investment in science and technology make this a career-defining platform for professionals who combine technical rigour with a passion for improving patient outcomes.