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 251–275 of 287 jobs
Director, Customers & Market Insights
Labcorp
Bangalore5+ Years · Hybrid13 SeptLead the development and execution of comprehensive global insights, market research, and competitive intelligence strategies for Labcorp's Biopharma Laboratory Solutions.
Sr. International RA Specialist
BD
Bangalore5+ Years · Onsite13 SeptSenior Regulatory Affairs professional responsible for supporting global medical device registrations and lifecycle activities across multiple international markets. The role combines regulatory strategy, technical documentation review, risk assessment, and cross-functional coordination to enable compliant market access.
GLNS Data & System Care – Manager
Pfizer
Chennai5+ Years · Hybrid13 SeptLead data accuracy, confidence, and stewardship priorities supporting Global Logistics & Network Services with robust data governance.
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.
Associate Manager - MQA Downstream
Pfizer
Vizag5+ Years · Onsite13 SeptLead manufacturing quality assurance activities across terminal sterilization, visual inspection and packaging operations, ensuring cGMP compliance and Pfizer quality standards on the production floor.
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.
Group Product Manager - GI Ortho (Solitra)
Sun Pharma Laboratories Ltd
Mumbai5+ Years · Onsite12 SeptGroup Product Manager role within the Gastro/Ortho business unit, responsible for strategic marketing, brand portfolio growth, profitability, market share, commercial planning, and product life-cycle management.
Clin Data Assoc II/Senior Clin Data Assoc
Thermo Fisher Scientific
Remote5+ Years · Remote12 SeptClinical Data Associate II/Senior Clinical Data Associate role supporting high-quality, analysis-ready clinical trial data through advanced data review, cleaning, reconciliation, query management, and inspection readiness.
Medical Writer, Clinical Development
Not specified
Ahmedabad5+ Years · Onsite12 SeptAuthor, review, and manage high-quality clinical and regulatory documentation that supports global clinical development programs, clinical trial execution, and regulatory submissions.
Customer Success Specialist (Pathology & Sequencing Labs)
Roche
Delhi NCR5+ Years · Hybrid12 SeptField-based customer success role providing scientific expertise, pre-sales support, installation, training, and technical assistance to pathology and sequencing laboratories across India.
Regulatory Labeling Manager
Amgen
Hyderabad5+ Years · Onsite12 SeptManage the planning, coordination, and execution of US regional regulatory labeling activities across the pharmaceutical product lifecycle.
MPD Head - Solitra
Sun Pharma Laboratories Ltd
Mumbai5+ Years · Onsite11 SeptLead pharmaceutical marketing strategy for the Solitra brand within the GI - Pain business unit, driving market growth, brand development, sales performance, customer engagement, and cross-functional execution across assigned markets.
Manager, Quality – Digital Systems
Pfizer
Chennai5+ Years · Remote11 SeptOwn and continuously improve Veeva eQMS operations within Regulatory Quality Assurance, serving as the bridge between business stakeholders and digital quality systems. Drive GxP-compliant administration, governance, reporting, cross-functional programs, AI-enabled transformation, and quality-system modernization.
Senior Analyst, Advanced Analytics
Labcorp
Bangalore5+ Years · Onsite11 SeptSenior analytics role focused on advanced SQL, statistical analysis, experimentation, dashboards, automation and AI-assisted workflows to turn marketing and commercial data into actionable business decisions.
Clinical Data Team Lead - External Data Acquisition
Thermo Fisher Scientific
Bangalore5+ Years · Remote11 SeptLead end-to-end external clinical data acquisition across multiple studies, ensuring accurate, timely, validated, and audit-ready integration of non-CRF data. Partner with vendors, clients, programmers, Data Standards, Clinical Operations, Biostatistics, and IT to deliver high-quality clinical data.
Sr Statistical Programmer(ADaM, TLF)
Syneos Health
Remote5+ Years · Remote11 SeptLead ADaM and TLF programming initiatives at Syneos Health to drive clinical trial success and data integrity.
Sr Associate Scientific Business Analyst
Amgen
Hyderabad5+ Years · Onsite11 SeptDrive digital capabilities and Research Informatics workflows for Large Molecule Discovery at Amgen as a Sr Associate Scientific Business Analyst.
Director, Process Development - Drug Substance
Amgen
Hyderabad5+ Years · Onsite11 SeptLead the new Drug Substance Technologies (DST) process development organization at Amgen Hyderabad, driving innovation in biomanufacturing and digital tools.
Senior Manager Clinical Sciences
Regeneron
Hyderabad5+ Years · Hybrid11 SeptLead clinical sciences operations within Regeneron's Hyderabad GCC by managing Clinical Data Reviewers and Medical Narrative Reviewers. Drive resource planning, quality governance, reviewer development, and operational excellence across the clinical development portfolio.
Senior Associate Software Engineer Salesforce
Amgen
Hyderabad5+ Years · Onsite11 SeptDrive Salesforce development, support, and continuous improvement for clinical artwork and supply chain solutions at Amgen.
Senior Specialist / Expert - Safety Medical Writer
Merck KGaA
Bangalore5+ Years · Onsite11 SeptSupport Global Patient Safety teams by producing high-quality pharmacovigilance medical-writing deliverables, including periodic safety reports, signal assessments, benefit-risk documents, risk-management plans, patient safety narratives, and health hazard reports.