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0-5 years
Not Disclosed
Bangalore, India
10 June 2, 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

Job Title: Manager – Clinical Data Management

Company: Thermo Fisher Scientific (PPD Clinical Research Portfolio)
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-based role
Travel: Frequent domestic and international travel required


About the Company

Thermo Fisher Scientific supports global clinical research and pharmaceutical innovation, working with top pharmaceutical companies and biotech organizations across 100+ countries. The organization has contributed to thousands of clinical trials, enabling the development of life-changing therapies worldwide.


Role Overview

The Manager – Clinical Data Management is responsible for leading a small team of clinical data management professionals, ensuring high-quality delivery of clinical data activities across projects. The role involves people management, resource allocation, process improvement, and collaboration with senior leadership to ensure timely and compliant execution of clinical data management tasks.


Key Responsibilities

1. Team Leadership & People Management

  • Manage a small team of clinical data management staff

  • Conduct:

    • Hiring and interviewing

    • Performance management

    • Coaching and mentoring

    • Employee development and counseling

  • Approve:

    • Time sheets

    • Expense reports

    • Leave requests

    • Overtime

  • Handle corrective actions and employee relations issues when required

2. Project & Portfolio Oversight

  • Ensure tasks are completed accurately, on time, and within budget

  • Support study teams in delivering high-quality clinical data management outputs

  • Monitor performance against client expectations

3. Resource Management

  • Manage resource allocation for assigned staff

  • Participate in global resourcing strategy and reporting

  • Coordinate staffing decisions with senior leadership

4. Quality & Compliance

  • Ensure adherence to:

    • Regulatory guidelines

    • Standard Operating Procedures (SOPs)

    • Client requirements

  • Maintain compliance in all clinical data management activities

5. Process Improvement

  • Contribute to development and improvement of:

    • Processes

    • Procedures

    • Training programs for clinical data management functions

6. Operational Support

  • Support implementation of operational activities across studies or portfolios

  • Assist study managers in ensuring smooth execution of data management tasks


Required Qualifications

  • Bachelor’s degree or equivalent qualification

  • Relevant academic or vocational training in related field

  • 0–5 years of overall experience (with at least 1+ year in leadership responsibility, preferred or required depending on profile)


Key Skills & Competencies

Leadership & Management

  • Ability to manage and motivate teams

  • Delegation and task supervision skills

  • Coaching and mentoring capabilities

  • Ability to set and track team timelines

Technical & Analytical Skills

  • Strong attention to detail

  • Numerical and analytical ability

  • Ability to act as a subject matter expert in DM processes

Communication Skills

  • Strong verbal and written communication

  • Good command of English grammar and professional communication

Problem Solving & Execution

  • Strong analytical and problem-solving skills

  • Ability to manage changing priorities and project demands

Compliance & Professional Conduct

  • Ability to maintain confidentiality of clinical and proprietary data

  • Understanding of regulatory guidelines and SOP adherence


Working Environment

  • Office-based role using standard office systems and tools

  • Frequent travel (domestic and international) required for site and project coordination

  • Exposure to clinical operations environment and regulatory workflows


Role Impact

  • Ensures high-quality clinical data management across global trials

  • Directly contributes to accuracy and reliability of clinical research data

  • Supports development of new therapies through efficient data operations

  • Plays a key leadership role in clinical trial execution