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 76–100 of 131 jobs

Quality Operations Specialist
Novartis
Hyderabad5+ Years · Hybrid25 SeptNovartis is seeking a Specialist, Quality Operations in Hyderabad to safeguard GxP conformity across its pharmaceutical quality management system. This role sits at the intersection of compliance, change control, audit readiness, and continuous improvement, directly supporting the delivery of safe, effective medicines. By managing change controls, GxP documentation, and quality KPIs, the specialist helps prevent compliance risks that could delay regulatory approvals or commercial supply. The position offers a compelling opportunity to work within a global healthcare leader, partner with cross-functional stakeholders, and deepen expertise in Novartis Quality Management Systems. For quality professionals seeking broad exposure to audits, investigations, and operational excellence, this role provides a strong platform for career progression in Hyderabad’s thriving life-sciences hub.

Senior Data Scientist – Surfaceome Biology
Amgen
Hyderabad5+ Years · Hybrid25 SeptAmgen's Bioinformatics Technologies group, part of the ARIA (Automation, Research Data Systems, Informatics, and AI) organization, is building the computational foundation for next-generation targeted and multispecific therapeutics. This Senior Data Scientist – Surfaceome Biology role sits at the precise intersection of AI/ML engineering and cell-surface biology, where systematic characterization of the surfaceome drives antigen discovery, protein density quantification, and internalization modelling. For a computational biologist based in India, this is a rare opportunity to work inside a global pharma discovery engine rather than a service vendor, shaping atlases and predictive models that directly nominate therapeutic candidates. The position delivers deep exposure to multi-omics integration, generative modelling, agentic AI and translational validation design, with a clear pathway into principal scientist or computational discovery leadership tracks.

Associate Director - Global Study Lead
Gsk
Bengaluru5+ Years · Hybrid25 SeptThis Associate Director–Global Study Lead role places you at the center of GSK’s clinical development engine in Bengaluru, leading the operational planning and delivery of a global clinical study. The position is pivotal to GSK’s mission of uniting science, technology, and talent to get ahead of disease, supporting therapeutic areas such as respiratory, immunology, oncology, HIV, and infectious diseases. You will work across clinical operations, data management, safety, regulatory, and external partners, translating asset strategy into flawless study execution. With visible impact on pipeline milestones and patient outcomes, this is a compelling opportunity for seasoned clinical operations professionals seeking global matrix leadership, process innovation, and a direct role in advancing GSK’s ambitious health impact goals.
Regulatory Affairs Manager
AstraZeneca
Mumbai5+ Years · Hybrid25 SeptAstraZeneca is seeking a Regulatory Affairs Manager in Mumbai to lead complex regulatory strategies for its innovative biopharmaceutical portfolio. This senior role sits at the intersection of science, compliance and commercial delivery, shaping submissions, lifecycle management and health-authority interactions across global and regional markets. The position is critical to accelerating patient access to medicines, ensuring filings are right first time and maintaining AstraZeneca’s reputation with regulators. You will advise cross-functional teams, mitigate regulatory risks and champion process improvements in a company known for scientific leadership. For an experienced regulatory professional, this is a high-visibility opportunity to influence pipeline decisions, mentor talent and work with global stakeholders. It offers a rare blend of strategic ownership, operational depth and career-defining exposure within one of the world’s leading patient-focused pharmaceutical companies.
Market Access Specialist
Roche
Delhi NCR5+ Years · Hybrid25 SeptRoche is seeking a Market Access Specialist to join its Access & Policy team in New Delhi, with coverage across Delhi and Haryana. This senior role is central to Roche's mission of expanding equitable healthcare access in India across oncology, ophthalmology, rare diseases and neurology. The position shapes evidence-based, innovative programs that strengthen health systems, support state-level partnerships, and improve prevention, early detection, screening and quality of care for underserved populations. Working closely with State Access Partners, government bodies, public health organizations and internal cross-functional teams, the incumbent translates strategy into scalable, measurable impact. For professionals passionate about health policy, access and system transformation, this is a rare opportunity to influence public-private collaboration at scale while advancing a global leader's patient-access agenda in India.

Clinical Study Manager II
ICON
Bangalore5+ Years · Hybrid24 SeptManage day-to-day clinical trial activities and lead planning, execution, monitoring, and issue resolution for complex clinical studies. The role supports sponsor-dedicated clinical development programmes while ensuring regulatory compliance, data integrity, quality, timelines, and efficient resource utilization.
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).

Head of Manufacturing and Supply Services Hyderabad Hub
Sanofi
Hyderabad5+ Years · Hybrid23 SeptLead and direct large-scale manufacturing and supply operations and teams (400+ personnel) at the Hyderabad Hub.

Clinical Data Coordinator II (CDC II)
ICON
Bangalore2-5 Years · Hybrid23 SeptDeliver high-quality clinical data management tasks, maintaining eCRFs, data validation specifications, and supporting study metrics.

Sr Professional Quality Management
Syneos Health
Hyderabad2-5 Years · Hybrid22 SeptSr Professional Quality Management Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. Job Responsibilities Job Summary Performs various activities (analysis, investigation, reporting, administration) related to ‘GXP’ (e.g. Good Clinical Practice or Good Pharmacovigilance Practice) and related topics for Clinical departments (therapeutic areas and functions).

Associate Manager SRC Governance
Sanofi
Hyderabad5+ Years · Hybrid22 SeptOur Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. Main responsibilities: Committee review Governance team support to set up governance to review meetings for all 4 committee reviews for ESRs, Phase 1 studies, Global Health Studies and MRPTC as per the established operating model. Study Review Committee (SRC) Primary responsibility is to Set up governance to review approval meetings for all 4 committee reviews - Company Sponsored Studies & Externally Sponsored Collaborations (CSS & ESC), ISS, Global Health Studies as per the established operating model. Identify stakeholders, organize pre-SRC meetings, maintain Action Registers, and manage audit readiness. Medico-Regulatory Pharmacovigilance Transversal Committee (MRPTC) Lead the conduct of the MRPTC including preparatory meetings, minutes, follow-up, and stakeholder coordination. Phase I SRC Set up governance for Phase 1 study review approval meetings, ensure cross-functional alignment, and manage risks and timelines.
Medical Affairs Manager
Johnson & Johnson
Mumbai5+ Years · Hybrid22 SeptMedical Affairs leadership role supporting DePuy Synthes country strategy, evidence generation, stakeholder engagement, innovation and medical/scientific activities.
Clinical Trial Manager
Astellas
Bangalore2-5 Years · Hybrid22 SeptClinical Trial Manager responsible for planning, setting up, and executing assigned clinical trials while coordinating cross-functional teams, vendors, investigators, sites, budgets, timelines, and trial deliverables in compliance with GCP, ICH, SOPs, and regulatory requirements.
Associate, Associate Database Analyst, Clinical Database Management
Pfizer
ChennaiFreshers · Hybrid21 SeptAssociate-level Clinical Database Management role supporting data monitoring, query management, database design, clinical data systems, documentation quality, and process improvement.
Centralized Monitoring Analyst (Level I & II)
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid21 SeptCentralized Monitoring Analyst role supporting clinical trials through analysis of operational and patient data, identification of trends and risks, documentation of findings and centralized monitoring activities.
Engineering Analyst, YouTube Trust and Safety
Google
Hyderabad2-5 Years · Hybrid20 SeptAs an Engineering Analyst on the YouTube Trust and Safety team, you will be directly responsible for ensuring that we effectively identify and remove disruptive content and users as quickly as possible.
Sr MSL - Heart Health
Bayer
Delhi NCR5+ Years · Hybrid20 SeptDrive scientific engagement and education with key thought leaders as a Senior Medical Science Liaison specializing in Heart Health at Bayer.

Clinical Data Coordinator - Senior
ICON
Bangalore5+ Years · Hybrid19 SeptSenior Clinical Data Coordinator supporting sponsor-dedicated clinical research programmes through clinical data management planning, discrepancy resolution, cross-functional collaboration, study documentation, data reconciliation, coding, cleaning, and mentoring of junior coordinators.
Senior Software Engineer - Networking & Automation
Cisco
Bangalore5+ Years · Hybrid19 SeptJoin the DSE PI common (PI NeXT) team to test and automate cutting-edge platform-independent networking components for Data Center solutions.
AWS DevOps Engineer
Infosys Limited
Bangalore2-5 Years · Hybrid19 SeptJoin Infosys Limited as an AWS DevOps Engineer to aid consulting teams in designing, deploying, and supporting cloud solutions.

Lead Clinical Data Science Programmer
ICON
Bangalore5+ Years · Hybrid18 SeptLead the design, development and validation of clinical data science programming solutions for complex clinical trials. Provide technical leadership, ensure data quality and integrity, collaborate across clinical functions, and mentor junior programmers.

Manager, Clinical Operations
Syneos Health
Hyderabad5+ Years · Hybrid18 SeptManage and provide operational leadership to Clinical Operations staff across study startup, site activities, monitoring and close-out. Oversee people, quality, regulatory compliance, resourcing, metrics and project delivery while supporting customer requirements and operational planning.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid18 SeptSenior Clinical Data Associate role supporting clinical data cleaning, database activities, query management, data review, study-specific processes, reporting, and training within a global clinical research organization.
Manager CMC Regulatory Affairs
Regeneron
Hyderabad5+ Years · Hybrid18 SeptManager-level CMC Regulatory Affairs role supporting global clinical regulatory submissions, CMC compliance, investigational product release, cross-functional coordination, and team leadership in Hyderabad.
Quality Engineering, QA Expert, Commissioning & Qualification Audit and Inspection Support
Lonza
Hyderabad5+ Years · Hybrid18 SeptQA Expert role providing Global Quality Engineering oversight for commissioning and qualification, CAPEX projects, audits, inspections, remediation, CAPA, and cGMP compliance.
