Pharma, Clinical Research & Healthcare Jobs in India
518 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 1–17 of 17 jobs
Assistant Clinical Project Manager
Clario
India Remote0-2 Years · Remote7 OctSupports Clinical Project Managers in coordinating medical imaging clinical studies from startup through closeout, including documentation, deliverables, study communications, financial follow-up and operational activities.
Senior Manager, Clinical Operations (FSP)
Thermo Fisher Scientific
Remote5+ Years · Remote4 OctSenior clinical operations leadership role responsible for managing clinical operations staff, FSP client relationships, resource allocation, performance management, quality, training and operational delivery across clinical trials.
Medical Writer
Thermo Fisher Scientific
Remote2-5 Years · Remote3 OctMedical Writer responsible for producing high-quality clinical and scientific documents for pharmaceutical and CRO clients, supporting projects from planning through final delivery in a fully remote India role.
Patient Reimbursement Coordinator - India
Syneos Health
Remote0-2 Years · Remote30 SeptCoordinate patient travel and reimbursement services for clinical trial participants, ensuring timely support, accurate processing, confidentiality, GCP compliance, and adherence to study-specific policies.
Principal Clinical Programmer (Rave EDC)
Syneos Health
Remote5+ Years · Remote29 SeptSenior clinical programming leadership role focused on Rave EDC programming, custom functions, clinical database development, technical support, study oversight, quality review, and program-level leadership across multiple clinical studies.
Manager, Medical Writing FSP
Thermo Fisher Scientific
Remote5+ Years · Remote28 SeptLead Medical Writing operations by managing writers, allocating resources, overseeing clinical and regulatory deliverables, maintaining quality and compliance, supporting proposals and business development, and developing team training programs.
Regulatory Consultant (CMC-EU, GCC & AU)
Syneos Health
Remote5+ Years · Remote27 SeptLead CMC regulatory authoring, lifecycle management, and global submissions across EU, GCC, and AU markets.
Medical Writer
Thermo Fisher Scientific
Remote2-5 Years · Remote26 SeptMedical Writer responsible for producing high-quality medical and scientific documents across clinical research programs. The role supports clinical study reporting, regulatory documentation, scientific communication and delivery of accurate, compliant client-ready content.
Clinical Document Agent (2nd Shift - 2 PM to 11 PM IST)
Syneos Health
Remote2-5 Years · Remote23 SeptCreate and manage clinical project documentation, subject files and electronic documentation while converting raw study data into electronic formats and ensuring compliance with established clinical procedures and quality requirements.
Manager, Medical Writing FSP
Thermo Fisher Scientific
Remote5+ Years · Remote19 SeptManager, Medical Writing FSP leading Medical Writers, resource planning, clinical document delivery, quality review, regulatory writing, training, and client-facing Medical Writing activities within a global clinical research organization.
Principal Clinical Programmer (Rave Programming)
Syneos Health
Remote5+ Years · Remote17 SeptLead complex Rave programming and clinical programming activities across multiple studies, providing technical expertise, quality oversight, project leadership and mentorship within clinical data management and clinical solutions.
Compliance Manager - APAC
Thermo Fisher Scientific
Remote5+ Years · Remote17 SeptLead GxP audit and regulatory inspection readiness and management across APAC, with responsibility for quality compliance, risk assessment, CAPA, audit reporting and continuous improvement across clinical research programs.
Senior Regulatory Affairs Associate- Clinical Trial Application
Parexel
Remote5+ Years · Remote16 SeptLead end-to-end Clinical Trial Application submissions across EU CTR and Rest of World regions, coordinating global regulatory projects, timelines, documentation, stakeholders and risk management to support compliant clinical-trial submissions.
Pharmacovigilance Physician
Thermo Fisher Scientific
Remote5+ Years · Remote16 SeptPharmacovigilance Physician role providing medical oversight of drug safety activities across the pharmaceutical product lifecycle, including case review, safety signal assessment, aggregate reports, regulatory submissions and benefit-risk evaluation.
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.
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.
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.