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Assoc Clin Data Team Lead

Thermo Fisher Scientific
0-2 years
5-10 LPA
Bangalore, Remote, India, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Clinical Data Team Lead

Company: Thermo Fisher Scientific
Department: Clinical Data Management
Work Schedule: Monday–Friday (Standard)
Work Environment: Office-Based
Job Type: Full-Time


Experience Level

  • Bachelor's degree or equivalent qualification required

  • 0–2 years of Clinical Data Management experience

  • Suitable for:

    • Clinical Data Coordinator

    • Clinical Data Associate

    • Clinical Data Analyst

    • Junior Clinical Data Manager

  • Entry-Level to Early Career Professional


Salary

Estimated market salary: ₹5–10 LPA CTC in India, with candidates having prior CRO or Clinical Data Management experience potentially earning ₹10–12 LPA.


Role Summary

The Associate Clinical Data Team Lead supports Lead Data Managers in managing clinical trial data activities. The role involves study setup, data cleaning, database testing, documentation management, quality review, study reporting, and coordination of data management activities across clinical research projects.


Key Responsibilities

Clinical Data Management

  • Support study setup and database preparation activities.

  • Assist in database specifications and build processes.

  • Participate in User Acceptance Testing (UAT).

  • Support database lock and close-out activities.


Data Cleaning & Quality Control

  • Coordinate data cleaning activities.

  • Review clinical data for completeness and accuracy.

  • Ensure quality standards and project timelines are maintained.

  • Support issue identification and resolution.


Project Coordination

  • Assist Lead Data Managers on assigned studies.

  • Monitor project timelines and deliverables.

  • Escalate project risks when required.

  • Support resource planning and forecasting activities.


Documentation & Reporting

  • Create and maintain project documentation.

  • Generate study status reports and metrics.

  • Track study progress and data management performance indicators.

  • Maintain audit-ready documentation.


Team Support & Training

  • Deliver study-specific training to junior team members.

  • Support onboarding and development of new associates.

  • Assist in delegation and coordination of project tasks.


Client & Stakeholder Interaction

  • Participate in client and project meetings.

  • Support communication between project teams and stakeholders.

  • Contribute to risk management discussions.


Required Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Biomedical Sciences

    • Related disciplines

Experience

  • 0–2 years of Clinical Data Management or Clinical Research experience.

  • Freshers with relevant academic background may also be considered depending on company requirements.


Key Skills

  • Clinical Data Management (CDM)

  • Clinical Trials

  • Data Cleaning

  • Database Validation

  • Query Management

  • Clinical Documentation

  • Project Coordination

  • Risk Management

  • Quality Control

  • Microsoft Excel

  • Communication Skills


Preferred Knowledge

  • ICH-GCP Guidelines

  • Clinical Trial Lifecycle

  • Electronic Data Capture (EDC) Systems

  • Clinical Databases

  • Regulatory Compliance

  • CRO Environment


Soft Skills

  • Attention to Detail

  • Analytical Thinking

  • Problem Solving

  • Team Collaboration

  • Time Management

  • Adaptability

  • Customer Focus


Travel Requirement

  • Primarily office-based role.

  • Occasional domestic or international travel may be required.

  • Occasional visits to study sites.


Ideal Candidate

A Life Sciences or Pharmacy graduate with an interest in Clinical Research and Data Management, strong analytical skills, attention to detail, and the ability to manage multiple tasks while ensuring data quality and regulatory compliance.


Career Path

  • Associate Clinical Data Team Lead

  • Clinical Data Manager

  • Senior Clinical Data Manager

  • Lead Data Manager

  • Project Data Manager

  • Clinical Operations Manager

  • Director – Clinical Data Management