Clinical Data Team Lead – Veeva
Company: Thermo Fisher Scientific (PPD Clinical Research Services)
Location: Bangalore, India | Fully Remote
Job Type: Full-Time | Remote
Work Schedule: Standard (Mon–Fri)
Experience: Typically 4+ Years (Clinical Data Management)
Qualification: Bachelor’s Degree in Life Sciences or Related Discipline
Salary Range: Not Specified
Job Overview
Thermo Fisher Scientific is seeking a Clinical Data Team Lead with experience in Veeva EDC to manage and lead clinical data management activities across clinical trial projects.
The Clinical Data Team Lead will act as the lead data manager for one or more studies, overseeing end-to-end data management processes including study setup, conduct, and closeout. The role involves coordinating with cross-functional teams and clients, ensuring data quality, compliance, and timely delivery of project milestones.
This position plays a critical role in managing clinical trial data operations, mentoring team members, and ensuring efficient execution of data management strategies.
Key Responsibilities
1. Clinical Data Management Leadership
Act as lead data manager for assigned clinical studies.
Oversee end-to-end data management activities including setup, conduct, and closeout.
Guide team members on applying protocol requirements to daily tasks.
Ensure high-quality data management deliverables.
2. Project Coordination & Client Communication
Act as liaison between project teams, management, and clients.
Communicate project status and data management updates regularly.
Collaborate with stakeholders to ensure smooth study execution.
Support project planning and coordination activities.
3. Documentation & Reporting
Develop and maintain data management documentation.
Perform independent review of deliverables as per CDM guidelines.
Generate project-specific status reports and study metrics.
Ensure proper tracking and documentation of all study activities.
4. Training & Team Development
Develop and deliver study-specific training for team members.
Mentor junior staff and provide guidance on data management tasks.
Support skill development and knowledge sharing within the team.
5. Project Planning & Resource Management
Assist in project forecasting, including effort estimation and resource planning.
Identify out-of-scope activities and support contract modification processes.
Assist in administrative and financial management of projects.
Ensure projects are delivered within timelines and quality standards.
6. Business Development Support
Participate in bid preparation and proposal activities.
Represent data management in bid defense meetings when required.
Support business growth initiatives within the organization.
7. Compliance & Quality Assurance
Ensure compliance with GCP guidelines and SOPs.
Maintain confidentiality of clinical and client data.
Ensure adherence to regulatory requirements and quality standards.
Required Skills
Clinical Data Management
Strong understanding of end-to-end clinical data management processes.
Experience with Veeva EDC systems.
Knowledge of clinical trial workflows including setup, conduct, and closeout.
Experience in oncology trials is preferred.
Leadership & Team Management
Ability to lead and mentor team members.
Experience managing study teams and coordinating activities.
Strong decision-making and leadership skills.
Project Management & Organization
Strong organizational and time management skills.
Ability to manage multiple projects and deadlines.
Experience in project planning and resource allocation.
Communication & Interpersonal Skills
Strong written and verbal communication skills.
Ability to interact with clients and cross-functional teams.
Excellent interpersonal and collaboration skills.
Analytical & Problem-Solving Skills
Strong analytical thinking and problem-solving abilities.
Attention to detail and data accuracy.
Ability to identify and resolve project-related issues.
Compliance & Domain Knowledge
Knowledge of GCP guidelines and regulatory requirements.
Understanding of SOPs and clinical data standards.
Ability to maintain confidentiality and data integrity.
Preferred Qualifications
Experience in pharmaceutical or CRO clinical research environment.
Hands-on experience with Veeva EDC systems.
Experience in oncology clinical trials.
Exposure to business development and bid processes.
Key Competencies
Clinical data management leadership
End-to-end study management
Project planning and execution
Team mentoring and development
Data quality and compliance
Client communication and coordination
Process optimization and reporting
About the Company
Thermo Fisher Scientific is a global leader in scientific services and technologies, supporting research, drug development, and healthcare innovation worldwide.
Through its clinical research division, PPD Clinical Research Services, the organization provides end-to-end clinical trial services including clinical operations, data management, regulatory affairs, and medical writing.
Operating in more than 100 countries with over 100,000 employees globally, the company partners with pharmaceutical and biotechnology organizations to accelerate the development of innovative therapies and deliver life-changing treatments to patients around the world.
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Siliguri |Illinois :
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