Senior Clinical Data Team Lead

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 5+ years). Prior experience must reflect lead(end-to-end) responsibilities. 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.