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2+ years
Not Disclosed
Bangalore, India
10 May 29, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: 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

Clinical Data Team Lead

Company: Thermo Fisher Scientific
Work Schedule: Standard (Monday–Friday)
Work Environment: Office-Based


About the Role

Thermo Fisher Scientific is seeking a Clinical Data Team Lead to oversee and coordinate clinical data management activities for research studies and clinical trials.

In this role, you will act as the lead data manager for one or more studies or support senior lead data managers on larger projects. You will be responsible for managing data management operations, coordinating with internal teams and clients, mentoring junior staff, and ensuring high-quality study execution.

Thermo Fisher Scientific has supported:

  • Top 50 pharmaceutical companies

  • 750+ biotechnology companies

  • 2,700+ clinical trials

  • Operations across 100+ countries over the last 5 years


Key Responsibilities

1. Clinical Data Management Operations

  • Apply study protocol requirements to daily data management activities.

  • Guide team members on protocol implementation and study procedures.

  • Independently perform assigned data management activities with high attention to quality and efficiency.

  • Ensure adherence to:

    • Regulatory guidelines

    • SOPs

    • Client expectations


2. Project Coordination & Client Communication

  • Act as a liaison between:

    • Project Leads

    • Clients

    • Internal teams

  • Communicate study progress and data management activities to management.

  • Produce project-specific:

    • Status reports

    • Study metrics

    • Operational updates


3. Documentation & Quality Review

  • Develop and maintain:

    • Data management documentation

    • Study files

    • Project tracking records

  • Perform independent reviews of data management deliverables according to Clinical Data Management (CDM) guidelines.

  • Monitor study-level metrics and project performance indicators.


4. Training & Mentorship

  • Develop and deliver study-specific training for data management staff.

  • Mentor and support junior team members on study-related activities.

  • Assist teams in maintaining compliance with processes and quality standards.


5. Resource & Financial Management

  • Assist with:

    • Project forecasting

    • Resource planning

    • Workload estimation

  • Identify potential out-of-scope activities and communicate them to management.

  • Support contract modification processes when required.

  • Assist with administrative and financial management of assigned projects.


6. Business Development Support

  • Participate in business development activities when required.

  • Assist with:

    • Bid preparation

    • Bid defense meetings

    • Client presentations


Educational Qualifications

Required Education

  • Bachelor’s degree or equivalent qualification in a relevant field.

  • Equivalent combinations of:

    • Education

    • Training

    • Directly related experience
      may also be considered.


Experience Requirements

  • Minimum 2+ years of relevant experience in:

    • Clinical Data Management

    • Clinical research operations

    • Study coordination

    • Related fields


Required Skills & Competencies

Technical & Regulatory Skills

  • Ability to apply:

    • Regulatory guidelines

    • SOPs

    • Clinical data management processes

  • Comfortable using interactive computer programs and data management systems.

  • Ability to maintain confidentiality of:

    • Clinical data

    • Client proprietary information


Analytical & Organizational Skills

  • Strong:

    • Organizational skills

    • Analytical thinking

    • Problem-solving abilities

    • Attention to detail

  • Ability to manage timelines and adapt to changing project demands.

  • Ability to work independently with minimal supervision.


Communication & Leadership

  • Strong written and verbal communication skills.

  • Excellent command of English language and grammar.

  • Strong interpersonal and customer-focused approach.

  • Ability to:

    • Train and direct study teams

    • Mentor junior staff

    • Collaborate effectively across teams


Personal Attributes

  • Proven flexibility and adaptability.

  • Positive team-oriented mindset.

  • Ability to work both independently and collaboratively.


Working Conditions

  • Office-based work environment.

  • Exposure to standard office equipment.

  • Occasional travel:

    • Domestic

    • International

  • Occasional site visits as required.


Why Join Thermo Fisher Scientific?

At Thermo Fisher Scientific, you’ll become part of a global organization committed to:

  • Scientific innovation

  • Operational excellence

  • Collaboration

  • Professional growth

  • Improving global healthcare outcomes

You’ll work in an environment where teamwork, learning, and impactful contributions are valued every day.


About Thermo Fisher Scientific

Thermo Fisher Scientific is a global leader in scientific research, healthcare, and laboratory solutions, supporting pharmaceutical, biotechnology, and healthcare organizations worldwide to accelerate innovation and improve patient outcomes.