Pharma, Clinical Research & Healthcare Jobs in India
518 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 1–25 of 41 jobs
Medical Affairs Operations Executive
AstraZeneca
Mumbai2-5 Years · HybridTodayAstraZeneca, a global science-led biopharmaceutical leader, seeks a Medico Marketing Excellence Executive in Mumbai to drive end-to-end support for medical affairs and VEEVA-led events. This role is pivotal in ensuring that medical education, advisory boards, and scientific exchange activities are executed with rigor, compliance, and financial transparency. By safeguarding zero breaches in documentation and processes, the executive directly contributes to AstraZeneca's ability to deliver life-changing medicines and maintain trust with healthcare professionals. This is a compelling opportunity for a scientifically grounded professional to build a career at the intersection of medical affairs, project management, and operational excellence within a top-tier pharma company. You will collaborate across Medical, Marketing, Compliance, Legal, and IT, gaining broad exposure to commercial and medical functions while championing patient-centric innovation.
Analyst Graphic Designer I – Medical Publications
AstraZeneca
Bengaluru2-5 Years · HybridYesterdayAstraZeneca is hiring an Analyst Graphic Designer I – Medical Publications in Bengaluru to create accurate, publication-ready visuals and layouts for scientific communications. The role is hybrid and calls for at least three years of regulated medical, healthcare or scientific publishing design experience.
Senior Associate, Central Monitor, Data Surveillance, Clinical Data Sciences
Pfizer
Chennai2-5 Years · Hybrid8 days agoPfizer is recruiting a Senior Associate, Central Monitor in Chennai to run risk-based monitoring of subject data in clinical trial databases. The job involves configuring and testing the RBM system at study level, defining key risk indicators and following up on signal and action resolution with global study teams.
Senior Associate, Data Manager, Clinical Data Sciences
Pfizer
Mumbai2-5 Years · Hybrid10 days agoPfizer is hiring a Senior Associate, Data Manager, Clinical Data Sciences in Mumbai on a hybrid basis. The role manages clinical trial data monitoring and management activities and works with local and global experts to maintain data quality.

Global QMS Manager
Novartis
Hyderabad2-5 Years · Hybrid27 days agoNovartis is hiring a Global QMS Manager in Hyderabad to oversee compliance and governance of Batch Release Hub configurations and related quality systems. The role works across Quality, IT and business teams on system changes, validation, documentation and global user support.
Sr. Associate, Basic Results Author
Pfizer
Chennai2-5 Years · Hybrid7 OctPfizer is hiring a Sr. Associate, Basic Results Author in Chennai to prepare and maintain clinical trial results disclosures for public registries. The role focuses on accurate, compliant authoring and review of clinical trial results while working with cross-functional study and disclosure teams.

Medical Writer II (MLR Reviewer)
Syneos Health
Delhi NCR2-5 Years · Hybrid2 OctMedical Writer II responsible for scientific writing, publication deliverables and medical-legal-regulatory review readiness. The role combines end-to-end medical writing, Veeva document management, MLR review, publication planning and cross-functional collaboration.

Clinical Data Programmer II
Novotech
India2-5 Years · Hybrid2 OctDrive core clinical trial programming, database design, and data validation activities at a leading global CRO, ensuring strict compliance with GCDMP and ICH-GCP standards.

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.
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.

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 II Reg Strategy, GRS Oncology
Pfizer
Chennai2-5 Years · Hybrid30 SeptSupport global regulatory strategy and lifecycle maintenance activities for oncology products, coordinating submissions, CMC Module 1 documentation, labeling, safety compliance activities, Health Authority responses, and cross-functional regulatory operations.

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.
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.
Medical Science Liaison
Bayer
Delhi NCR2-5 Years · Hybrid29 SeptDrive scientific engagement and education as a Medical Science Liaison with Bayer in Delhi.

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.
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.

Safety Physician (MBBS) | Pharmacovigilance Medical Review | Immediate Joiners Preferred
Syneos Health
Delhi NCR2-5 Years · Hybrid28 SeptPerform medical review and interpretation of adverse-event and aggregate safety information for investigational and marketed products, ensuring pharmacovigilance, regulatory, SOP, and project-specific compliance.

Site Start Up EUCTR II
Parexel
Hyderabad2-5 Years · Hybrid26 SeptSupport complex clinical trial initiation, focusing on EU CTR compliance and CTIS database management.

Senior Biostatistician
Iqvia
Bengaluru2-5 Years · Hybrid26 SeptThe Senior Biostatistician at IQVIA in Bengaluru is a strategic, client-facing role at the intersection of clinical trial design, regulatory-grade evidence, and advanced analytics. IQVIA supports pharmaceutical, biotechnology, and medical device sponsors across global programs, so this position directly influences how studies are powered, analyzed, and reported. The role owns statistical methods sections, analysis plans, datasets, and tables, listings, and figures (TLFs) while guiding junior staff and collaborating with data management, clinical, and programming teams. It is compelling for professionals who want to deepen expertise in CDISC, ICH-GCP, and modern trial methodology while gaining leadership exposure, budget accountability, and direct client interaction. It also offers a pathway into principal, team lead, or sponsor-side biostatistics roles in India’s rapidly expanding life-sciences market.

Maintenance Planner and Scheduler
Novartis
Hyderabad2-5 Years · Hybrid25 SeptThis Maintenance Planner and Scheduler role at Novartis in Hyderabad is critical to keeping pharmaceutical manufacturing operations compliant, reliable, and inspection-ready. The position sits at the intersection of engineering, quality assurance, and production, ensuring that calibration and maintenance activities are planned, executed, and documented in line with GMP expectations. By managing master data in SAP, COMOS, and CMX, monitoring work order backlogs, and supporting audits, the planner directly enables uninterrupted supply of medicines. For professionals with an engineering background and German language skills, this is a compelling opportunity to gain deep exposure to Novartis’s global technical operations, work on continuous improvement projects, and build a career in pharmaceutical maintenance and compliance. It offers a rare blend of hands-on scheduling, cross-functional collaboration, and strategic site reliability impact.

Area Medical Advisor - Hepatology
Gsk
Bengaluru2-5 Years · Hybrid25 SeptGSK’s Area Medical Advisor, Specialty, Hepatology is a field-facing Medical Affairs role based in Bengaluru, designed to be the scientific bridge between GSK’s hepatology portfolio and the external clinical community. You will translate complex clinical data into credible, on-label scientific exchange with Key External Experts, gastroenterologists, hepatologists and institutional stakeholders. As GSK advances specialty medicines and vaccines across respiratory, immunology, oncology, HIV and infectious diseases, hepatology remains a critical therapy area where medical evidence, real-world insights and compliant scientific engagement shape brand strategy and patient outcomes. This position offers a rare blend of clinical science, strategic influence and cross-functional leadership, ideal for a physician seeking to deepen therapeutic expertise, build KOL networks and influence the standard of care in liver disease across India.

Senior Forecasting Analyst
Novartis
Hyderabad2-5 Years · Hybrid25 SeptNovartis is seeking a Senior Forecasting Analyst to join its Strategy & Growth team in Hyderabad, supporting pipeline and lifecycle forecasts that shape commercial and investment decisions across the global portfolio. This role sits at the intersection of epidemiology, commercial strategy, and data analytics, requiring deep pharmaceutical domain knowledge and the ability to translate complex data into actionable forecasts. The successful candidate will influence board-level reviews and BD&L opportunity assessments for therapeutic areas, helping Novartis prioritize pipeline assets and optimize lifecycle management. It is an exceptional opportunity for pharma forecasting professionals to work on high-impact global products, collaborate with cross-functional leaders, and build advanced modeling capabilities using real-world and clinical trial data.
Clinical Data Team Lead
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid25 SeptLead clinical data management activities for clinical research studies, coordinating data management teams, clients, project leads, documentation, training, metrics and study deliverables.
Key Account Manager - Aesthetics
AbbVie
India2-5 Years · Hybrid24 SeptDrive strategic account relationships, market access, and contracting for leading aesthetics brands at Allergan Aesthetics (AbbVie).
