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
Not Disclosed
10 Dec. 30, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Job Title: Associate Clinical Data Team Lead (Remote – India)
Job ID: R-01338261
Job Type: Full-time
Category: Clinical Research
Location: Remote, India (Fully Remote)


About the Role

Thermo Fisher Scientific’s Clinical Research Services team is at the forefront of accelerating innovative therapies to market. With a track record of supporting the top 50 pharmaceutical companies and 750+ biotech organizations across 2,700 clinical trials in over 100 countries, we bring unmatched scientific and clinical expertise to global drug development.

We are seeking a highly motivated Associate Clinical Data Team Lead (ACDTL) to support our Clinical Data Management (CDM) projects. In this role, you will assist the Lead Data Manager in ensuring high-quality, compliant, and timely delivery of clinical data across all study phases.


Key Responsibilities

  • Assist the Lead Data Manager in study setup, data cleaning, database close-out, and related CDM activities.

  • Apply study protocol components to daily tasks, ensuring adherence to regulatory guidelines, SOPs, and client expectations.

  • Provide study-specific training and mentorship to junior data associates.

  • Coordinate data cleaning activities and delegate tasks to ensure timely delivery of high-quality data.

  • Contribute to database specifications, database build, user acceptance testing, and edit check development.

  • Monitor project risks, escalate issues, and maintain comprehensive data management documentation.

  • Participate in team and client meetings, providing support for risk management and resource forecasting.

  • Generate and review study metrics and project-specific status reports for management and clients.

  • Review data management deliverables to ensure accuracy and regulatory compliance.


Required Qualifications

  • Bachelor’s degree in Life Sciences, Pharmacy, or a related field. Advanced degrees are advantageous.

  • Minimum 3–5 years of experience in Clinical Data Management or relevant clinical research roles.

  • Hands-on experience with RAVE / Veeva EDC systems.

  • Strong understanding of clinical trial protocols, regulatory requirements, and data management processes.


Skills & Competencies

  • Excellent written and verbal communication skills in English.

  • Strong organizational, analytical, and problem-solving skills with attention to detail.

  • Ability to work independently with minimal supervision while maintaining high confidentiality.

  • Proficient in training, mentoring, and guiding junior team members.

  • Demonstrated flexibility, adaptability, and ability to manage timelines effectively.

  • Strong interpersonal skills and customer focus, capable of collaborating within global teams.


Working Conditions

  • Work performed in an office or clinical environment with exposure to standard office equipment.

  • Occasional travel to clinical sites may be required.


Career Growth & Opportunities

As part of our FSP Data Management team, you will support a globally recognized biopharmaceutical sponsor, gaining exposure to advanced CDM workflows, AI-enabled data platforms, and global clinical trials. This role offers multiple career paths, including progression to Senior CDM, CDTL, CDM Project Manager, or transition into Data Standards/Programming roles, based on skills, performance, and business needs.

Why Join Thermo Fisher Scientific?

  • Gain global exposure across clinical studies, therapeutic areas, and international collaborations.

  • Contribute to end-to-end study delivery from set-up to close-out.

  • Strengthen your analytical, project management, and risk management skills in a rapidly evolving clinical research environment.

  • Be part of a company with a mission-driven culture, annual revenue exceeding $44B, and a commitment to innovation, patient safety, and scientific excellence.


About Thermo Fisher Scientific

Thermo Fisher Scientific is a world leader in serving science. Our 90,000+ global colleagues deliver innovative technologies and pharmaceutical services through leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, and Patheon. Learn more at www.thermofisher.com.

Equal Opportunity Employer – Thermo Fisher Scientific fosters an inclusive workplace for all employees.


Apply Now to be part of a team that transforms clinical research and brings life-changing therapies to patients worldwide.