Sr Clin Data Team Lead

Work Schedule

Environmental Conditions

Job Description

Location: Bulgaria, Hybrid (2 days in 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.
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.