Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Assoc Clin Data Team Lead

Thermo Fisher Scientific
Thermo Fisher Scientific
3-5 years
₹10 LPA to ₹16 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

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

Thermo Fisher Scientific is hiring an Associate Clinical Data Team Lead (ACDTL) in India – Fully Remote to support global clinical data management operations for international clinical trials. In this role, you will act as an assistant lead data manager, helping oversee clinical study data management activities including study setup, database development, data cleaning, and database lock activities. You will collaborate with lead data managers, clinical research teams, and global stakeholders to ensure clinical data quality, regulatory compliance, and timely project delivery. This role is ideal for professionals with experience in clinical data management, electronic data capture systems such as RAVE or Veeva EDC, and clinical trial data quality processes. The estimated salary for this role ranges from ₹10 LPA to ₹16 LPA depending on experience in clinical data management and clinical trial operations.

Key Responsibilities

  • Support the Lead Data Manager in managing clinical data management activities for assigned studies.

  • Coordinate data cleaning tasks and ensure high-quality clinical data standards are maintained.

  • Assist with study setup, database specifications, database build, and user acceptance testing (UAT).

  • Monitor project timelines, risks, and data management deliverables to ensure deadlines are met.

  • Create and maintain clinical data management documentation and project records.

  • Deliver study-specific training to junior data management associates.

  • Participate in team meetings and client discussions to support project delivery.

  • Generate study metrics, status reports, and project updates for stakeholders.

  • Support resource planning and project forecasting activities for clinical data management tasks.

Required Qualifications

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

  • 3–4.6 years of experience in clinical data management or clinical research roles.

  • Hands-on experience with EDC systems such as Medidata RAVE or Veeva EDC.

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

Required Skills

  • Clinical Data Management (CDM)

  • Electronic Data Capture Systems (RAVE / Veeva EDC)

  • Clinical Trial Data Cleaning & Database Management

  • Project Coordination & Risk Monitoring

  • Data Quality Control & Regulatory Compliance

  • Clinical Study Documentation

  • Team Collaboration & Training

Salary

Approximate Salary: ₹10,00,000 – ₹16,00,000 per year (depending on experience in clinical data management, EDC systems, and clinical trial data operations).