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5+ years
₹10 – ₹15 LPA
Bangalore, India
15 Aug. 6, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Thermo Fisher Scientific – Senior Clinical Data Team Lead

Role Overview

Domain: Clinical Data Management (CDM)
Department: Clinical Research Services
Work Schedule: Second Shift (Afternoons)
Work Environment: Office-based
Role Level: Senior / Team Lead Level

Experience Required

Required Experience: 5+ years of Clinical Data Management experience

Preferred experience:

  • Clinical Data Manager

  • Senior Clinical Data Associate

  • Lead Data Manager

  • Clinical Trial Data Management roles

  • CRO or pharmaceutical clinical research experience

Educational Qualification

  • Bachelor’s degree or equivalent qualification

Suitable backgrounds:

  • B.Pharm / M.Pharm

  • Life Sciences

  • Biotechnology

  • Healthcare-related disciplines

  • Clinical Research qualifications

Package / Salary Expectation (India)

Thermo Fisher has not disclosed salary details for this position.

Expected CTC range:

Experience

Approximate Package

5 years CDM experience

₹10 – ₹15 LPA

6–8 years CDM experience

₹14 – ₹22 LPA

Senior Lead/Project Lead experience

₹20 – ₹30+ LPA

Actual salary depends on:

  • Clinical Data Management experience

  • EDC system expertise (Medidata Rave, Oracle Clinical, Veeva, etc.)

  • CDISC knowledge

  • Team management experience

  • CRO/pharma background

  • Location and negotiation

Key Responsibilities

  • Lead clinical data management activities for complex studies.

  • Act as the main Data Management contact for project teams and clients.

  • Manage study timelines, quality, risks, and deliverables.

  • Review and apply clinical protocols to data management processes.

  • Monitor study metrics and escalate issues.

  • Support:

    • Resource planning

    • Budget forecasting

    • Bid preparation

    • Client discussions

  • Lead high-volume and complex clinical trials.

  • Mentor junior CDM team members.

  • Ensure compliance with:

    • ICH-GCP guidelines

    • SOPs

    • Regulatory requirements

Required Skills

  • Strong Clinical Data Management knowledge

  • Clinical trial lifecycle understanding

  • EDC systems expertise

  • Data review and query management

  • Risk-based quality management

  • Clinical database concepts

  • Medical terminology

  • Project coordination skills

  • Client communication skills

  • Team leadership ability

  • Advanced Excel and reporting skills

Career Growth

Senior Clinical Data Team Lead
Clinical Data Manager / Lead Data Manager
CDM Project Manager
Associate Director – Clinical Data Management
Director – Clinical Data Management

Fit for B.Pharm/M.Pharm Candidates

  • Fresher: Not suitable

  • 1–3 years experience: Not suitable directly

  • 3–5 years CDM experience: May be considered depending on skills

  • 5+ years CDM experience: Strong match

Overall Assessment

This is a high-value CDM leadership role suitable for professionals who have already built experience in clinical trial data management, EDC systems, data cleaning, query management, and study leadership. For a B.Pharm/M.Pharm candidate, the typical pathway is:

Clinical Data Associate → Senior Clinical Data Associate → Clinical Data Manager → Senior Clinical Data Team Lead.