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 111 jobs
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.
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 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.
Senior Manager, Analytics Products and Technology - Obesity
Amgen
Hyderabad5+ Years · Onsite21 SeptOwn the development and evolution of business-facing analytics and decision-support products for Amgen's global obesity business.
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.
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.
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.
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.
Specialist Quality Complaints
Amgen
Hyderabad5+ Years · Onsite16 SeptQuality Specialist role responsible for end-to-end global product complaint processes, complaint investigations, record quality, procedural compliance and continuous improvement within Amgen's quality organization.
Sr Sales Specialist, Reproductive & Genetic Health
Illumina
Hyderabad5+ Years · Remote16 SeptDrive commercial growth and market development for Illumina's reproductive and genetic health portfolio across India by developing strategic customer relationships, increasing clinician engagement, supporting genomic workflow adoption, and commercializing new applications.
Principal Safety & PV Specialist (Literature CP & Review)
Syneos Health
Hyderabad5+ Years · Onsite16 SeptLead pharmacovigilance literature case processing, safety review, and team workflows as a Principal Safety & PV Specialist based in Gurugram or Hyderabad.
Sr Associate Software Engineer
Amgen
Hyderabad5+ Years · Onsite16 SeptContribute to the design, development, and deployment of advanced Customer Identity and Access Management (CIAM) solutions as a Sr Associate Software Engineer at Amgen.
Director, Global Clinical Trial Services, India
Regeneron
Hyderabad5+ Years · Onsite15 SeptDirector-level clinical operations leader responsible for clinical trial delivery in India, providing operational leadership, building local capabilities and ensuring high-quality, compliant execution across the trial lifecycle.
Manager - International Regulatory Lead
Amgen
Hyderabad5+ Years · Onsite13 SeptLead international regulatory strategy and execution for Amgen products across international countries. The role provides regulatory expertise for product development, registrations, lifecycle management, labeling strategy and health-authority interactions while coordinating global, regional and local stakeholders.
Director - Manufacturing CMC Project management
Eli Lilly and Company
Hyderabad5+ Years · Onsite13 SeptOwn the end-to-end Manufacturing CMC commercialization strategy for assigned pharmaceutical products from post-Phase 2 through launch and beyond. Lead cross-functional product teams, drive executive visibility, manage risks and align development, manufacturing, supply chain and regulatory stakeholders.
Study Grants Manager
Novartis
Hyderabad5+ Years · Hybrid13 SeptManage the financial planning foundation for clinical research by translating study protocols into grant plans and Fair Market Value assessments. Partner with global, regional and local clinical teams to improve site activation, forecasting accuracy and operational efficiency.
Senior Specialist, Global Partnerships & Trial Optimization
Regeneron
Hyderabad5+ Years · Hybrid13 SeptSupport global clinical trial optimization through feasibility analysis, enrollment planning, patient recruitment strategy, data analytics, KPI reporting, and technology-enabled solutions across Regeneron's Global Development organization.
Manager Central Monitoring
Regeneron
Hyderabad5+ Years · Hybrid12 Sept## Job Description ### Build our future together Regeneron develops and commercializes medicines for serious diseases through science and innovation across drug development, manufacturing, and commercialization. ### Your Role The Manager, Central Monitoring, Data Analysis will join the Global Clinical Trial Services team in Hyderabad. The role oversees centralized monitoring activities for global and complex clinical trials and supports configuration, execution, and maintenance of Risk-Based Quality Management (RBQM) platforms. The position combines programming, data analysis, workflow automation, data-system integration, and clinical trial risk management. The role may oversee multiple studies within an assigned therapeutic area, lead process-improvement initiatives, and collaborate with cross-functional teams and industry partners to advance central monitoring capabilities. ### Discover Your Role - Act as a subject-matter expert for Central Monitoring RBQM platform configuration, implementation, and execution. - Maintain Central Monitoring Key Risk Indicator and Quality Tolerance Limit libraries. - Configure studies and develop Central Monitoring configuration specifications with stakeholders. - Provide operational expertise, training, guidance, and escalation support. - Conduct central monitoring reviews, data refreshes, and troubleshooting. - Apply programming expertise to data analysis, automation, reporting, and system integration. - Interpret KRI and KPI data to support decision-making. - Contribute to technology, system, process, and training standardization. - Represent Central Monitoring in process-improvement initiatives. - Oversee multiple studies within an assigned therapeutic area where applicable. - Travel up to 25% as required. ### Requirements At least 7 years of relevant biotechnology or pharmaceutical industry experience and at least 2 years of direct RBQM systems experience are required. The role requires database design, system configuration, report development, programming, clinical development knowledge, ICH/GCP knowledge, clinical database and EDC experience, analytical skills, and strong communication. CluePoints or similar centralized monitoring/RBQM experience is preferred.
Team Lead - Scientific Writing
Sanofi
Hyderabad5+ Years · Onsite12 SeptLead scientific writing operations for assigned therapeutic areas, partnering strategically with scientific communication stakeholders while leading and developing expert and senior writers. Drive high-quality scientific, clinical, medical, publication and education deliverables with strong compliance, process excellence and technology adoption.
Specialist Mfg 1
Amgen
Hyderabad5+ Years · Onsite12 SeptSpecialist role supporting AI-enabled manufacturing innovation across Amgen's global manufacturing network. The position bridges manufacturing subject matter experts and technical development teams to deliver compliant, scalable digital capabilities.