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Clin Data Team Lead

Thermo Fisher Scientific
Thermo Fisher Scientific
3-5 years
₹14 LPA to ₹22 LPA
Remote
10 March 11, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Team Lead – Thermo Fisher Scientific (Remote, India)

Thermo Fisher Scientific is hiring a Clinical Data Team Lead (CDTL) in India – Fully Remote to manage clinical data management operations for global clinical trials. In this role, you will serve as the lead data manager for one or more clinical studies, overseeing end-to-end clinical data management activities including study setup, database build, data validation, data cleaning, and database lock. You will collaborate with clinical project leaders, data management teams, and global stakeholders to ensure that clinical trial data meets quality standards, regulatory requirements, and project timelines. This role is suitable for professionals with strong experience in clinical data management, EDC systems such as Medidata RAVE or Veeva EDC, and leadership within clinical research teams. The estimated salary for this role ranges from ₹14 LPA to ₹22 LPA depending on experience in clinical data management and leadership of clinical trial data operations.

Key Responsibilities

  • Lead clinical data management activities for assigned clinical studies from setup to database lock.

  • Apply project protocol requirements to daily data management workflows and guide team members.

  • Act as a primary liaison between project leadership, clients, and data management teams.

  • Develop and maintain clinical data management documentation and project files.

  • Review data management deliverables to ensure compliance with quality and regulatory standards.

  • Monitor study metrics, timelines, and project progress, generating status reports for stakeholders.

  • Deliver study-specific training and mentorship to data management team members.

  • Support project forecasting, resource planning, and identification of out-of-scope work.

  • Participate in business development activities including bid preparation and proposal support.

  • Contribute to administrative and financial management of clinical data management projects.

Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field.

  • 4–5.6 years of experience in clinical data management or clinical research roles.

  • Experience with Electronic Data Capture (EDC) platforms such as Medidata RAVE or Veeva EDC.

  • Strong understanding of clinical trial processes, regulatory guidelines, and data quality standards.

Required Skills

  • Clinical Data Management (CDM) Leadership

  • Electronic Data Capture (RAVE / Veeva EDC)

  • Clinical Trial Data Quality & Validation

  • Database Build & Data Cleaning

  • Project Management & Resource Planning

  • Stakeholder Communication & Client Coordination

  • Team Training & Mentorship

Salary

Approximate Salary: ₹14,00,000 – ₹22,00,000 per year (depending on experience in clinical data management leadership, EDC systems, and clinical trial data operations).