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 51–64 of 64 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.
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.
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 Programmer II
Syneos Health
Pune2-5 Years · Remote11 SeptClinical programming role supporting clinical data management and drug development projects through SAS and clinical database technologies, with responsibility for programming, validation, documentation, quality and project delivery.
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.
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.
Associate Manager, Data Operations - FS
Premier Research
Remote5+ Years · Remote10 SeptLead data operations within Premier Research’s Functional Services Provider team, combining people leadership, data acquisition project management, quality oversight and customer relationship management to support clinical research programs.
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.
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.
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.
Clinical Trial Coordinator II - FSP
Thermo Fisher Scientific
Remote2-5 Years · Remote9 SeptSupports global clinical trial delivery by coordinating study documentation, site activation, feasibility, regulatory tracking, eTMF/CTMS activities, and project administration. The role contributes to audit readiness, quality delivery, and timely site start-up across assigned clinical trials.