Clinical Data Team Lead – Veeva
Company: Thermo Fisher Scientific
Location: Bangalore (Fully Remote)
Job Type: Full-Time
Category: Clinical Research / Clinical Data Management
Work Schedule: Monday to Friday
Job Overview
Thermo Fisher Scientific is hiring a Clinical Data Team Lead – Veeva to oversee clinical data management activities for global clinical trials. This role is responsible for leading end-to-end data management processes, ensuring data integrity, and maintaining compliance with regulatory standards, Good Clinical Practices (GCP), and standard operating procedures.
The Clinical Data Team Lead will serve as the primary data management lead for one or more studies, coordinate cross-functional activities, and act as a key liaison between project teams, clients, and stakeholders. This position offers an opportunity to contribute to high-impact clinical research programs supporting global pharmaceutical and biotechnology organizations.
Key Responsibilities
Clinical Data Management Leadership
Lead data management activities for clinical studies with limited to moderate complexity.
Apply project protocol requirements to daily data management tasks and guide team members accordingly.
Act as the primary liaison for project leads, clients, and internal stakeholders on data management activities.
Mentor and train junior data management staff on study processes and deliverables.
Project Management and Documentation
Develop, maintain, and review data management project documentation.
Perform independent reviews of data management deliverables in accordance with clinical data management guidelines.
Generate and present project status reports and monitor study metrics.
Support resource planning, forecasting, and identification of potential out-of-scope activities.
Assist in administrative and financial management of assigned projects.
Operational and Quality Oversight
Ensure compliance with regulatory requirements, global SOPs, and client expectations.
Independently perform data management tasks with a strong focus on quality and accuracy.
Deliver study-specific training for project staff to ensure operational consistency.
Monitor timelines and ensure project deliverables meet defined quality standards.
Business and Stakeholder Engagement
Support business development activities including bid preparation and bid defense meetings when required.
Collaborate with cross-functional teams to ensure effective study execution.
Maintain effective communication with management regarding study progress and data management activities.
Education Requirements
Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related discipline, or equivalent qualification.
Equivalent combination of education, training, and relevant experience may be considered.
Experience Required
Minimum 4+ years of experience in a Clinical Data Management role.
Hands-on experience with Veeva Electronic Data Capture (Veeva EDC).
Proven end-to-end clinical data management experience including study setup, conduct, and closeout.
Experience in oncology clinical trials preferred.
Experience working in pharmaceutical, biotechnology, or contract research organization environments is advantageous.
Required Skills and Competencies
Strong understanding of clinical trial processes, data validation, and regulatory requirements.
Excellent organizational, analytical, and problem-solving skills.
Strong leadership and mentoring capabilities.
Effective written and verbal communication skills with strong English proficiency.
Ability to manage multiple priorities and meet project timelines.
Strong attention to detail and data quality standards.
Ability to work independently and collaboratively within global teams.
High level of professionalism and ability to maintain confidentiality of clinical data.
Work Environment
Office or remote work environment supporting global clinical operations.
Occasional travel to clinical sites may be required depending on project needs.
Career Growth and Benefits
Opportunity to work on global clinical trials across multiple therapeutic areas.
Exposure to advanced clinical data management technologies and global research processes.
Professional development opportunities within a leading clinical research organization.
Collaborative work environment focused on innovation and scientific excellence.
Competitive compensation and comprehensive employee benefits.
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