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 126–150 of 159 jobs
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.
Regulatory AI & Automation Specialist
Roche
Hyderabad2-5 Years · Onsite17 SeptDrive hands-on AI, machine learning, document intelligence, and workflow automation for global regulatory operations, improving regulatory document processing, submission dossier management, compliance tracking, and operational efficiency.
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.
Senior Associate, Organizational Design & Analytics
Amgen
Hyderabad2-5 Years · Onsite16 SeptSupport organizational designs, workforce-planning activities, hiring governance, and data analytics as a Senior Associate 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.
Associate Data Scientist - Investment Analytics
Amgen
Hyderabad2-5 Years · Onsite15 SeptJoin Amgen's Marketing Investment Optimization team in Hyderabad to drive data-driven decision-making using advanced analytics and modeling.
Senior Machine Learning Platform Engineer
Amgen
Hyderabad2-5 Years · Onsite14 SeptDesign, build, and scale enterprise-grade ML and generative-AI platform capabilities. Bridge platform engineering, MLOps, and GenAI to establish reusable APIs, automated pipelines, and developer infrastructure across enterprise AI initiatives.
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.
Principal Scientific Writer
Sanofi
Hyderabad5+ Years · Onsite12 SeptJoin Sanofi's Business Operations team as a Principal Scientific Writer to lead complex medical communications, publication plans, and scientific content creation across key therapeutic areas.
MODA Specialist
Lonza
Hyderabad0-2 Years · Hybrid12 SeptSupport compliant and efficient execution of MODA Environmental Monitoring activities, maintaining master data accuracy, validation documentation, data integrity and audit readiness.
Regulatory Labeling Manager
Amgen
Hyderabad5+ Years · Onsite12 SeptManage the planning, coordination, and execution of US regional regulatory labeling activities across the pharmaceutical product lifecycle.
Senior Project Associate (3rd Shift)
Syneos Health
Hyderabad2-5 Years · Hybrid12 SeptDrive and support project management activities to ensure successful execution of complex clinical trials during 3rd shift operations.
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Manager, Clinical Trial Risk Analyst
Bristol Myers Squibb
Hyderabad2-5 Years · Onsite11 SeptLead clinical trial risk monitoring and risk-based management activities by translating clinical data into actionable risk insights. Partner with cross-functional study teams to identify critical risks, establish KRIs and QTLs, monitor signals, and support data-driven trial oversight.
Tech Compliance Analyst II
Syneos Health
Hyderabad2-5 Years · Hybrid11 SeptJoin Syneos Health as a Tech Compliance Analyst II to manage software validation and compliance for global life sciences solutions.