Pharma, Clinical Research & Healthcare Jobs in India

Sr. Mgr, Sales Training

AbbVie

Senior sales training leader responsible for designing, delivering and sustaining training interventions for AbbVie's therapeutic business and improving field-force productivity.

(Sr) Project Manager, Feasibility Site Activation

ICON

Senior Project Manager role focused on Study Start-Up, feasibility and site activation for global clinical studies. The position owns SSU strategy and execution, regulatory and ethics pathways, site contracts, timelines, risks and cross-functional delivery.

Director, CDM Programming

Thermo Fisher Scientific

Senior leadership role overseeing Clinical Data Management Programming operations, people, resources and project delivery. The position drives departmental strategy, quality, compliance, client engagement and innovation within Thermo Fisher Scientific's clinical research organization.

CDC II

ICON

Support 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.

Senior CDA/ Clin Data Assoc II

Thermo Fisher Scientific

Perform 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.

Study Grants Manager

Novartis

Manage 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

Support 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.

Manager Central Monitoring

Regeneron

## 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.

Clinical Trial Specialist

Astellas

Support 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.

Customer Success Specialist (Pathology & Sequencing Labs)

Roche

Field-based customer success role providing scientific expertise, pre-sales support, installation, training, and technical assistance to pathology and sequencing laboratories across India.

MODA Specialist

Lonza

Support compliant and efficient execution of MODA Environmental Monitoring activities, maintaining master data accuracy, validation documentation, data integrity and audit readiness.

Senior Manager Clinical Sciences

Regeneron

Lead 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.

KOL Engagement Specialist

Astellas

Support compliant engagement with healthcare professionals and key external experts across congresses, events, funding, and grants while enabling efficient Medical Affairs operations.

Principal Biostatistician

ICON

Lead 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.

Pharmacovigilance Associate

ICON

Process and assess clinical trial and post-marketing safety cases while ensuring accurate, timely, and compliant pharmacovigilance activities. Support case intake, triage, coding, narratives, quality control, follow-up, and regulatory compliance.

TMF Specialist (All Levels)

ICON