Pharma, Clinical Research & Healthcare Jobs in India
512 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 376–400 of 423 jobs
CDM PM
Thermo Fisher Scientific
Bangalore5+ Years · Remote14 SeptLead clinical data management projects and programs from operational, quality, timeline and financial perspectives. Serve as a primary client liaison while coaching data-management teams, managing resources and budgets, mitigating project risks and ensuring delivery across clinical studies.
CDC II
ICON
Bangalore2-5 Years · Hybrid13 SeptSupport clinical data management activities for clinical trials by maintaining eCRFs and validation specifications, reconciling clinical and third-party data, monitoring study metrics and resolving data issues. The role contributes to high-quality clinical data delivery within a global clinical research organisation.
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.
API Marketing Manager
Sun Pharmaceutical Industries Ltd
Mumbai5+ Years · Onsite13 SeptDrive API business growth across assigned regulated international markets by combining market intelligence, business development, customer relationship management and cross-functional execution. Own regional sales targets, identify opportunities and develop strategies to expand the API customer base, market share and revenue.
Senior CDA/ Clin Data Assoc II
Thermo Fisher Scientific
Bangalore2-5 Years · Hybrid13 SeptPerform clinical data management and data cleaning activities for clinical trials while ensuring compliance with GCP, SOPs and client requirements, with responsibility for specialized processes and support to junior staff.
Associate I-Reg CMC Strategy
Pfizer
Chennai0-2 Years · Onsite13 SeptProvide regulatory CMC strategy and documentation support for product license renewals and annual reports across global markets, with a focus on post-approval regulatory requirements.
Head Analytical Development
Abbott
Mumbai2-5 Years · Onsite13 SeptLead analytical and product development activities within Abbott's Established Pharmaceutical Products division, supporting new product opportunities, development teams and business plans.
Senior Specialist Submission Management
Merck Group
Bangalore5+ Years · Onsite13 SeptSenior regulatory submission management specialist responsible for planning, compiling, publishing, quality-checking, and dispatching regulatory submissions while ensuring compliance, data integrity, and submission timelines.
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.
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.
Associate II - Reg CMC Strategy
Pfizer
Chennai2-5 Years · Onsite13 SeptSupport CMC regulatory strategy for global License Renewals and Annual Reports, preparing and coordinating CMC dossier contributions, applying regulatory requirements and managing submission activities under the guidance of regulatory leadership.
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.
PK Medical Writer
ICON
Bangalore2-5 Years · Remote12 SeptDevelop and deliver high-quality Clinical Pharmacology & Pharmacometrics documents, including population PK/PD plans and reports, CSRs, protocols, and regulatory clinical documents. The role supports clinical research projects through scientific writing, document coordination, quality control, and cross-functional collaboration.
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.
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.
Associate Data Manager - FS
Premier Research
Regional_India_402-5 Years · Remote12 SeptAssociate Data Manager supporting Premier Research's Functional Services Provider team, responsible for clinical data review, database quality, data queries, data management planning, CRF/edit-check testing, and clinical data listing validation.
Clinical Trial Specialist
Astellas
Bangalore2-5 Years · Hybrid12 SeptSupport the end-to-end operational delivery of assigned clinical trials at Astellas, working with Clinical Trial Leads, Clinical Trial Managers, sites, CROs, vendors, and global cross-functional teams. The role focuses on quality, compliance, accurate trial execution, and operational excellence.
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.
Quality Specialist II
Teva Pharmaceuticals
Bangalore2-5 Years · Onsite12 SeptQuality Specialist II responsible for pharmaceutical quality activities including CMC documentation review, analytical method and stability documentation, equipment qualification, BMR review, and Product Quality Review/Annual Product Review activities.
Production Planning Expert
Merck KGaA
Bangalore2-5 Years · Onsite12 SeptPlanning Specialist responsible for end-to-end production planning and coordination of New Product Introduction and Development projects at the Jigani site, including ERP master data governance, resource planning, capacity coordination, and structured handovers to routine planning teams.