Sr Clin Data Team Lead

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Data Team Lead

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

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.