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 1–6 of 6 jobs
Senior Medical Writer
Parexel
Bangalore5+ Years · Remote7 OctParexel is hiring a Senior Medical Writer for its India-Bengaluru-Remote team. The role focuses on clinical trial disclosure and transparency, with responsibilities spanning regulatory document writing, disclosure submissions, client guidance, project management, and mentoring.
Global Labelling Lead
ICON
Bangalore5+ Years · Remote15 SeptGlobal Labelling Lead responsible for regulatory labelling strategy, compliance, document management and cross-functional coordination for pharmaceutical or biotechnology development projects.
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.
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.
Clinical Data Analyst III
Parexel
Bangalore5+ Years · Remote10 SeptLead clinical data validation and data management activities across clinical studies, serving as a subject matter expert while ensuring data quality, regulatory compliance and successful database delivery.
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.