Pharma, Clinical Research & Healthcare Jobs in India
510 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 126–150 of 510 jobs
Assistant Clinical Project Manager
Clario
Bangalore0-2 Years · Remote1 OctSupport clinical project managers with study administration, financial tracking, cross-functional coordination, Salesforce configuration and clinical research operations while ensuring quality, compliance and timely delivery.
Medical Writing Specialist
Novo Nordisk
Bangalore5+ Years · Onsite1 OctSenior medical writing specialist role responsible for leading clinical reporting deliverables, setting direction for complex medical writing work, coordinating global stakeholders, and driving quality and process improvements across clinical development programmes.
Mgr, Regulatory Consulting (Office based)
Syneos Health
Hyderabad2-5 Years · Hybrid1 OctManager, Regulatory Consulting leads regulatory consulting projects, regulatory submissions, client engagements, project teams, and people-management activities while providing strategic and operational regulatory advice across pharmaceutical and related product development programs.
Scientific Writer HEVA
Sanofi
Hyderabad2-5 Years · Onsite1 OctScientific Writer – Health Economics and Value Assessment (HEVA) develops high-quality HEVA communications and evidence-based content supporting product value, access, and reimbursement decisions across global business units.
Senior Clinical Research Associate II
Pfizer
Mumbai5+ Years · Onsite1 OctLead and support moderately complex clinical research projects, overseeing study startup, monitoring plans, regulatory activities, budgets, drug supply, and site-level execution for pharmaceutical clinical studies.
Associate Medical Writer
Thermo Fisher Scientific
Mumbai0-2 Years · Remote1 OctSupport medical and scientific writing activities for clinical research programmes, including patient-centric documents, while coordinating with internal and external stakeholders and maintaining quality and regulatory compliance.
Senior Officer / Executive - Direct Procurement
Sun Pharmaceutical Industries Ltd
Mumbai2-5 Years · Onsite1 OctManage direct procurement of packaging materials for commercial sites and R&D locations, ensuring timely purchase orders, vendor coordination, delivery tracking, quality documentation, and procurement reporting.
Manager / Senior Manager - Medical Science Liaison
Eli Lilly and Company
Delhi NCR2-5 Years · Onsite1 OctField-based Medical Science Liaison role focused on Cardio-metabolic diseases, scientific exchange with healthcare experts, medical insights, strategic territory planning, and cross-functional collaboration.
Central Monitor Senior Associate
Amgen
Hyderabad2-5 Years · Onsite1 OctCentral Monitor Senior Associate independently performs proactive, data-driven central monitoring across clinical studies, using analytics and structured review to detect risks affecting patient safety, data quality, and protocol adherence.
Manager - Legal
Motherhood Hospitals
Bangalore5+ Years · Onsite1 OctLead all aspects of corporate legal operations, contract drafting, litigation management, and stakeholder advisory.
Access Field Manager
Novartis
Delhi NCR5+ Years · Onsite30 SeptThis Access Field Manager role at Novartis is a strategic market-access position focused on Delhi and surrounding states/UTs. It sits at the intersection of public health, government affairs, payer engagement and commercial strategy, ensuring that innovative Novartis therapies are included in state formularies and reach reimbursed beneficiaries through sustainable health-system solutions. The position is critical as India's healthcare access landscape becomes more decentralised, with state governments, public health bodies and payers shaping adoption pathways. By co-creating MoUs, disease awareness programmes, protocol shaping and alternative funding models, the Access Field Manager directly influences patient access and Novartis's long-term portfolio performance. This is a compelling opportunity for experienced healthcare strategy professionals who want to shape policy, build high-level partnerships and translate access barriers into measurable patient impact across Delhi's evolving health ecosystem.
Territory Business Manager – Derma (Dermatology Sales)
Abbott
Coimbatore0-2 Years · Onsite30 SeptAbbott's Established Pharmaceuticals Division (EPD) is expanding its dermatology franchise in Tamil Nadu, and the Territory Business Manager – Derma Prime role sits at the commercial frontline of that push. Operating across Coimbatore's consulting rooms, retail chemists and stockist network, this position converts clinical conviction into prescription volume for a portfolio of dermatology brands. The role matters because dermatology in India is a fast-growing, high-margin therapy area where market share is won through consistent doctor engagement rather than mass-market advertising. For an ambitious pharma sales professional, it offers the credibility of representing a global innovator, structured performance metrics around call average and coverage, and a clear pathway into area business management. The mandate is entrepreneurial: you own your geography's numbers, relationships and brand recall.
Territory Business Manager – Multitherapy (Pharma Field Sales)
Abbott
Mumbai0-2 Years · Onsite30 SeptAbbott's Established Pharmaceuticals Division (EPD) is a cornerstone of the company's emerging-markets strategy, delivering trusted, affordable branded generics across cardiology, diabetes, pain management and multi-therapy portfolios. The Territory Business Manager role is the frontline engine of that strategy in Mumbai, converting brand plans into prescriptions, market share and sustained revenue growth across a defined geography. The position matters because EPD's commercial success depends on deep physician relationships, disciplined territory execution and real-time field intelligence that shapes national marketing decisions. For ambitious pharma sales professionals, it offers structured exposure to a global MNC's compliance-led selling model, multi-specialty therapy knowledge, digital reporting discipline and a transparent, performance-linked career ladder into area sales management or brand marketing.
Regulatory AI & Content Specialist
Roche
Hyderabad5+ Years · Onsite30 SeptThis Regulatory AI & Content Specialist role at Roche India sits within Product Development Regulatory and Roche Services & Solutions, a strategic hub driving digital transformation of regulatory content. The position bridges regulatory affairs, structured content management, and generative AI, helping standardize reusable content for AI-powered authoring and automation. It is critical to Roche’s global submissions because high-quality, compliant regulatory documents accelerate approvals and support patient access. The specialist configures templates and metadata within Roche’s in-house GenAI platform, supports document authors, and ensures outputs are submission-ready. For regulatory professionals, this is a rare chance to combine ICH-CTD expertise with AI-enabled authoring, gaining future-facing skills in regulatory operations and platform governance while contributing to medicines that reach millions.
Associate Project Specialist - Medical Communications
Sanofi
Hyderabad2-5 Years · Onsite30 SeptThis Associate Project Specialist – Medical Communications role at Sanofi in Hyderabad sits within Sanofi Business Operations (SBO), a centralized hub supporting Specialty Care, Vaccines, General Medicines, Consumer Healthcare, and R&D. The position is pivotal to delivering high-quality scientific publications and medical education materials—slide decks, abstracts, posters, and manuscripts—that communicate Sanofi’s clinical evidence to healthcare professionals, regulators, and payers. By coordinating project timelines, compliance submissions, budgets, and stakeholder communication, the specialist ensures scientific writers can focus on content excellence. This is an exceptional opportunity for life-sciences graduates to gain end-to-end exposure to medical publications, publication management tools like iEnvision and PromoMats, and global medical affairs operations. It offers a launchpad into medical writing, publications management, or scientific communications leadership within a top-tier pharmaceutical company.
Project Manager – Medical Communications
Sanofi
Hyderabad5+ Years · Onsite30 SeptThis Project Manager – Medical Communications role at Sanofi Business Operations, Hyderabad, is a strategic enabler of scientific publication and medical education delivery across global therapeutic areas. As part of Scientific Communications Operations, the position coordinates publication planning, medical events, advisory boards, compliance submissions, and vendor budgets for slide decks, abstracts, posters, and manuscripts. It sits at the intersection of medical affairs, medical writing, and operational excellence, ensuring Sanofi's scientific narrative reaches healthcare professionals, regulators, and payers with accuracy and timeliness. The role is compelling because it combines project leadership, people mentoring, and cross-functional global stakeholder management within a top-tier biopharma. It also offers exposure to AI/GenAI-enabled workflows, ServiceNow ESM, iEnvision, PromoMats, and publication compliance tools—skills highly valued across India's growing medical communications and medical affairs hubs.
Engagement Analyst – External Expert Engagement Services
AstraZeneca
Bengaluru2-5 Years · Hybrid30 SeptThe Engagement Analyst role within AstraZeneca's External Expert Engagement Services (E3S) sits at the intersection of Medical Affairs, Commercial and Compliance operations. Based at Manyata Tech Park, Bangalore, this individual-contributor position governs the end-to-end lifecycle of engagements with healthcare providers and patients — advisory boards, consulting assignments and speaking programmes that shape how AstraZeneca's medicines are understood, prescribed and adopted. Because every such engagement carries transparency and anti-bribery obligations, the analyst protects AstraZeneca's licence to operate while accelerating scientific exchange. For professionals with 1–5 years of experience in regulated contracting or compliance workflows, the role offers global exposure, direct partnership with Medical Affairs, Nominated Signatories and Legal, and a clear pathway into compliance, medical affairs operations or risk management careers.
Associate Manager – Automation Engineering
Pfizer
Visakhapatnam5+ Years · Onsite30 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 – Automation role sits at the heart of this operation, ensuring that Emerson DeltaV DCS, PI Historian, and field instrumentation systems run reliably, safely, and in full compliance with GMP. This position is not just about maintaining equipment; it directly enables uninterrupted production of life-saving therapies. By joining Pfizer’s forward-thinking engineering team, you will work on complex automation projects, drive digital transformation, and collaborate with cross-functional experts. The role offers a compelling career opportunity for engineers seeking to deepen their expertise in pharmaceutical automation, validation, and compliance within a world-class organization.
Manager, Operational Excellence (Lean Six Sigma)
Pfizer
Visakhapatnam5+ Years · Onsite30 SeptThe Manager, Operational Excellence at Pfizer's Vizag manufacturing campus sits at the intersection of Lean Six Sigma methodology, GMP compliance and enterprise-wide continuous improvement. Operating inside Pfizer's Integrated Manufacturing Excellence (IMEx) framework, this role deploys the company's global operating system across a high-volume, regulated production site, converting shop-floor data into measurable performance gains. Because Vizag also supports translation and dossier execution documentation, the position directly influences inspection readiness and the speed at which Pfizer files and launches products in global markets. For a certified Black Belt, this is a rare opportunity to own programme governance, coach cross-functional teams and build capability at scale, with high visibility to senior leadership across manufacturing, quality, regulatory affairs and supply chain.
Director, Commercial Analytics - Obesity
Amgen
Hyderabad5+ Years · Onsite30 SeptLead global commercial analytics for Amgen's obesity business, driving strategy, sales execution, and U.S. market intelligence from Hyderabad.
Manager Biostatistics (Study Statistician and/or Study Lead Statistician)
Amgen
Hyderabad5+ Years · Onsite30 SeptProvide statistical expertise, lead clinical study analyses, and drive tech-enabled transformation in biostatistics at Amgen Hyderabad.
Pharmacovigilance Reporting Associate
ICON
Bangalore2-5 Years · Remote30 SeptSupports accurate and timely preparation, review and submission of pharmacovigilance safety reports for clinical trials and post-marketing activities. The role combines safety-report preparation, adverse-event data analysis, regulatory compliance and cross-functional collaboration.
Manager - Regulatory Affairs
Abbott
Mumbai5+ Years · Onsite30 SeptManage Regulatory CMC activities for assigned products, including registrations, submissions, lifecycle compliance, regulatory strategy, health-agency interaction and cross-functional coordination within Abbott's Established Pharmaceutical Products division.
Senior Global Regulatory Scientist
ICON
Bangalore2-5 Years · Hybrid30 SeptSenior Global Regulatory Scientist responsible for leading global clinical-trial regulatory activities, submission strategy, regulatory project teams, client deliverables, and compliance across pharmaceutical clinical trials in India.
Associate Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite30 SeptOwn and execute quality complaint activities across the global complaint process, ensuring compliant handling, accurate records, timely closure, and appropriate escalation. The role connects customer feedback with quality processes and continuous improvement.