Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Data Team Lead – Make an Impact at the Forefront of InnovationWe 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 timelinesWorking 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.