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 101–125 of 145 jobs
Scientist, Biomarker Analysis
Amgen
Hyderabad5+ Years · Onsite25 SeptAmgen's Scientist, Biomarker Analysis role in Hyderabad is a strategic addition to the Global Development - Precision Medicine organization, specifically within Computational Biology and Translational Analytics. As Amgen expands its India innovation footprint, this position will deliver high-quality clinical biomarker analytics across oncology, inflammation, rare disease, cardiovascular/metabolic, and obesity programs. The scientist will transform complex multi-omics, imaging, and clinical trial data into actionable translational insights that inform target engagement, patient stratification, mechanism validation, and benefit-risk decisions. This is a compelling opportunity for a quantitative biologist to work at the interface of drug development, advanced statistics, and responsible AI, influencing global portfolio decisions while helping build a high-impact precision medicine capability at Amgen India. The role offers deep scientific ownership, cross-functional collaboration, and exposure to late-stage clinical programs.
Associate Manager, Externally Sponsored Research
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi Business Operations (SBO) in Hyderabad seeks an Associate Manager, Externally Sponsored Research (ESR) to oversee investigator-sponsored studies and externally sponsored collaborations from concept submission through closeout. This role sits at the intersection of clinical research, medical governance, and operational excellence, ensuring that unsolicited research support requests are routed for scientific review and managed in compliance with Sanofi SOPs, ICH-GCP, and local regulations. It is critical to Sanofi's Specialty Care, Vaccines, General Medicines, and R&D pipelines because ESRs generate real-world evidence and expand research partnerships. The position offers deep exposure to global stakeholders, SRC coordination, study start-up, product supply, contracting, and audit readiness. For professionals with clinical trial project management experience, it is a compelling opportunity to build specialized expertise in externally sponsored research operations while contributing to compliant, timely delivery of studies that inform medical and commercial strategy.
R&D Global Regulatory Affairs CMC Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptSanofi’s Global Regulatory Affairs CMC & Device Organization seeks an R&D GRA CMC Lead in Hyderabad to shape regulatory strategies for pharmaceuticals, biologics, vaccines, and combination products. This senior role is central to Sanofi’s pipeline, bridging R&D, manufacturing, and health authorities such as the US FDA and EMA. The CMC Lead ensures dossiers meet global quality and compliance standards, accelerates approvals, and mitigates regulatory risks across the product lifecycle. As a strategic partner, the position influences cross-functional teams, regulatory policy, and digital innovation, including AI-enabled regulatory workflows. For experienced CMC professionals, this is a high-visibility opportunity to lead complex submissions, negotiate with regulators, and advance patient access to innovative therapies while growing within a world-class regulatory network.
Regulatory Affairs CMC Team Lead
Sanofi
Hyderabad5+ Years · Onsite25 SeptThis R&D GRA CMC Team Lead role at Sanofi in Hyderabad is a senior regulatory affairs leadership position within the Global Regulatory Affairs CMC & Device Organization. The incumbent will shape global Chemistry, Manufacturing, and Controls strategies for pharmaceuticals, biologics, vaccines, and combination products, directly influencing approval timelines and lifecycle management. As a critical bridge between technical development, manufacturing, and health authorities, this role ensures Sanofi's innovative therapies reach patients with speed and compliance. The position offers exceptional exposure to FDA, EMA, and other global regulators, matrixed project teams, and cutting-edge digital regulatory tools such as Veeva Vault. For regulatory professionals seeking to lead strategy, mentor specialists, and drive organizational change in a world-class biopharma environment, this is a compelling career step with significant influence on Sanofi's commercial and clinical pipeline.
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Scientific Writer II
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite24 SeptAuthor and coordinate high-quality regulatory and clinical documents by integrating scientific, medical, and regulatory input across cross-functional development teams. The role combines scientific writing, document strategy, timeline management, quality review, and regulatory documentation expertise.
Associate - IC Plan Design
Amgen
Hyderabad2-5 Years · Onsite24 SeptDesign, model, and execute field incentive compensation plans and sales contests at Amgen Hyderabad.
Director, Process Development- Drug Product
Amgen
Hyderabad5+ Years · Onsite24 SeptLead and build the Drug Product Technologies organization at Amgen Hyderabad, driving process development, digital transformation, and global biotech deliverables.
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.
Safety & PV Coordinator
Syneos Health
Hyderabad0-2 Years · Onsite23 SeptProcess ICSRs, perform safety tracking, and manage pharmacovigilance operations in an office-based role in Hyderabad.
Director, Process Development - Drug Product
Amgen
Hyderabad5+ Years · Onsite23 SeptLead the establishment and growth of Amgen's Drug Product Technologies organization in Hyderabad, building a high-performing team and operating model while expanding global drug product process-development capabilities through technical, digital and cross-functional innovation.
Associate- Quality Complaints
Amgen
Hyderabad2-5 Years · Onsite23 SeptManage assigned product complaint records and investigation activities within Amgen's global quality complaint process, ensuring procedural compliance, record quality, timely closure and continuous improvement.
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.
Regional Manager - Coronary & Renal Denervation
Medtronic
Hyderabad5+ Years · Remote22 SeptLead and coach a regional sales team to drive commercial growth and market adoption of advanced coronary and cardiovascular medical technologies at Medtronic.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite22 SeptDirector-level clinical operations leadership role responsible for clinical trial delivery across India, from feasibility through site close. The position leads India-based teams and FSP partners while coordinating with global functional leaders, sites, investigators, vendors, and regulatory authorities.
Regulatory Labeling Mgr
Amgen
Hyderabad5+ Years · Onsite21 SeptSupport the planning, coordination, and execution of EU and global labelling compliance activities within the Regulatory Affairs organisation.
Study Grant Analyst II
Parexel
Hyderabad2-5 Years · Remote21 SeptStudy Grant Analyst II responsible for developing and analyzing clinical study grants for Phase I-IV trials, supporting pre-sales proposals and awarded projects, and ensuring compliance with fair market value and healthcare regulations.
Global Executive Assistant Capability Support Specialist
Sanofi
Hyderabad2-5 Years · Onsite21 SeptProvides high-level administrative, coordination, and talent acquisition support to Sanofi's Global Executive Development and Global Capability teams. The role focuses on executive calendar management, travel, meetings, purchasing, vendor coordination, communications, and confidential information handling.
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.
Associate, Medicaid – Contracts & Pricing Execution (AIN)
Amgen
Hyderabad2-5 Years · Onsite18 SeptSupport U.S. Medicaid rebate operations within Amgen's Contracts & Pricing Execution function. Execute invoice, claim, validation, dispute, payment-package, reconciliation and documentation activities while maintaining compliance, controls and audit readiness.
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.
Seniorr Associate Regulatory Writing
Amgen
Hyderabad2-5 Years · Onsite17 SeptIndependently author and manage routine to moderately complex regulatory documents while coordinating reviews, ensuring scientific accuracy, inspection readiness and timely delivery across cross-functional teams.
Sr. Advisor/Director – Peptide Analytical Scientist
Eli Lilly and Company
Hyderabad5+ Years · Onsite17 SeptProvide scientific and technical leadership for peptide analytical development, supporting protein synthesis process development through experimental design, analytical method development, process understanding and technology transfer while leading a high-performing scientific team.
Specialist, Quality Operations
Novartis
Hyderabad5+ Years · Hybrid17 SeptManage quality operations, GxP compliance and quality-system projects within the assigned area, ensuring compliant execution of change controls, documentation, audits, investigations, reporting and governance activities.