Competitive sign-on bonus available for successful candidates.* *Terms and conditions apply.
Location: Sofia, Bulgaria (hybrid, 2 days in office)
Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 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
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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 and 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 clients’ 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.
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