Senior Clinical Data Team Lead

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

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 5+ years).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

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.