Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Office
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.
Skills Required
regulatory guidelines , Data Management, Sops
