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 226–249 of 249 jobs
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.
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.
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.
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.
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.
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 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.
Principal Biostatistician
ICON
Bangalore5+ Years · Hybrid11 SeptLead statistical strategy and delivery for Phase I-III oncology trials, serving as a senior statistical expert across protocols, statistical analysis plans, clinical reporting, data analysis and regulatory submissions while mentoring statisticians and supporting process improvement.
Document Lifecycle Management
Lonza
Hyderabad5+ Years · Onsite10 SeptOwn compliant GMP documentation lifecycle and QA oversight activities in Hyderabad, with responsibility for document archiving, true copy scanning, retention decisions and retain-sample disposition.
Project Data Manager
Syneos Health
Remote5+ Years · Remote10 SeptLead end-to-end clinical data management delivery for assigned projects, ensuring contractual commitments, quality standards, timelines, and sponsor expectations are met. Coordinate data management teams, manage project finances and resources, and provide client-facing leadership across study delivery.
Procurement Global Category Manager - Medical Communications
Amgen
Hyderabad5+ Years · Onsite10 SeptLead global procurement strategy for the Medical Communications category, driving strategic sourcing, supplier governance, innovation, stakeholder alignment, and measurable value across medical, commercial, marketing, and enterprise objectives.
Data Scientist – Technical Services & Manufacturing Sciences
Eli Lilly and Company
Hyderabad5+ Years · Onsite10 SeptDrive advanced analytics, predictive modeling, and digital innovation across pharmaceutical manufacturing and development. The role combines data science with GMP-regulated operations to improve process monitoring, optimization, quality, and data-driven decision-making.
Manager, Medical Writing FSP
Thermo Fisher Scientific
Remote5+ Years · Remote10 SeptLead medical writing operations for clinical research programs, managing writers, resources, deliverables, quality, timelines, training, and client-facing activities. The role combines scientific expertise, regulatory writing, people leadership, and clinical data interpretation within a global CRO environment.
Senior Regulatory Affairs Associate
Parexel
Bangalore5+ Years · Remote10 SeptLead end-to-end Clinical Trial Application submission activities across EU CTR and Rest of World regions, ensuring compliant, high-quality and timely regulatory delivery.