Clinical Data Team Lead - Veeva

Roles & Responsibilities
• Act as Lead Data Manager for one or more projects, owning end-to-end data management activities or supporting the Lead DM as required
• Lead DM activities for individual, limited volume/complexity studies with guidance from senior team members
• Apply project protocol requirements to daily DM tasks and guide team members on correct protocol application
• Serve as liaison to Project Lead and/or client, and communicate DM status, risks, and updates to management
• Develop and maintain data management documentation files and perform independent reviews of DM deliverables as per CDM guidelines
• Develop and deliver study-specific training for DM project staff and support team capability building
• Produce regular project status reports for management, Project Lead, and/or clients, and monitor study metrics
• Support forecasting of hours, identify resource needs, and flag potential out-of-scope activities, assisting with contract modification processes
• Mentor junior staff on study-related DM tasks and ensure quality delivery standards
• Assist with administrative and financial management of allocated projects while delivering DM activities independently with strong quality focus
• Support business development activities including bid preparation and participation in bid defense meetings where required

Qualification
• Bachelor’s degree or equivalent relevant academic/vocational qualification

Experience
• 4+ years of experience in a Clinical Data Manager role
• Strong hands-on working experience in Veeva EDC required
• End-to-end data management experience across Set-Up, Conduct, and Close-Out
• Oncology trial experience preferred

Skills
• Lead data management execution and client/stakeholder coordination
• Strong protocol understanding and ability to translate protocol into DM workflows
• CDM documentation management and independent deliverable review
• Study metrics monitoring, status reporting, and operational tracking
• Resource forecasting, scope management, and support for contract modification activities
• Team mentoring, training delivery, and study team direction
• Strong attention to detail, analytical/problem-solving skills, and structured execution
• Excellent written and verbal communication with strong English grammar
• Ability to work with minimal supervision while maintaining high confidentiality of clinical and proprietary data
• Strong customer focus, interpersonal skills, flexibility, and adaptability

About The Company
Thermo Fisher Scientific, through its PPD clinical research services portfolio, supports global clinical trials and data management delivery for leading pharmaceutical and biotech clients. With a mission to make the world healthier, cleaner, and safer, the organization offers collaborative teams, development opportunities, and technology-enabled clinical research services at scale across international studies.