Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Data Team Lead – Make an Impact at the Forefront of Innovation

We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in organizational performance. As a Senior Clinical Data Team Lead, you will act as a lead data manager for one or more projects and serve as a liaison to the Project Lead and/or client as required.

What You’ll Do:

• Applies relevant components of the project protocol to daily tasks and directs others on how to apply to their daily tasks. • Acts as an interdepartmental and client liaison for all DM study activities. • Produces project-specific status reports for management, Project Lead and/or clients on a regular basis. • Monitors and analyzes study metrics and escalates per the organization's risk management processes. • May participate in business development activities by assisting with bid preparation and representing data management at bid defense meetings, where required. • Assists with project forecasting of hours and identification of resource requirements. • Assists with the oversight of project budgets including identification of potential out of scope work and participation in the Contract Modification process. • Leads, high volume/highly complex studies. • Independently leads and delegates tasks to ensure timely completion of project activities to project timelines, quality and budget. • Mentors junior level staff on all associated tasks within a study. • Assists with administrative and financial oversight for allocated projects. • Communicates with management regarding all data management activities within their studies.

Education and Experience Requirements:

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 10+ years).
• Should have Hands on experience in Veeva EDC,
• Should have hands on experience in Set Up , Conduct and Close Out Activities
• Should have 2+ years of experience as Lead Data Manager role for one or multiple studies

Knowledge, Skills and Abilities: • Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations • Ability to use interactive computer programs • Good written/ verbal communication skills with a strong command of English language and grammar; good organizational, analytical/problem solving skills and attention to detail • Ability to work productively in both a team environment and independently as needed • Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data • Strong customer focus and excellent interpersonal skills. • Ability to direct and train study team • Ability to act as a study or department expert for DM processes • Ability to support project resourcing and project timeline planning and adherence to timelines

Working Conditions and Environment: • Work is performed in an office environment with exposure to electrical office equipment. • Occasional drives to site locations with occasional travel both domestic and international.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.