Sr. Clinical Data Associate

Work Schedule

Environmental Conditions

Job Description

Join Us as a Senior Clinical Data Associate – 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 Associate, you will perform all aspects of the data cleaning process, with minimal supervision, in accordance with Good Clinical Practices (GCP) and Standard Operating Procedures/Work Process Documents (SOPs/WPDs), to assess the safety and efficacy of investigational products and/or medical devices.
What You’ll Do:

• Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required.

• Reviews data listings for accuracy and consistency of data.

• Acts as point person and subject matter expert for specialized study-specific processes.

• Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database (EDC) as required.

• Contributes to the improvement of data management processes on a global level.

• Produces project-specific status reports for management and/or clients on a regular basis.

• Provides training and work direction to junior staff as required.

Education and Experience Requirements:

• Bachelor’s degree or equivalent, with relevant formal academic or vocational qualifications.

• Prior experience in clinical research, including hands-on experience managing and handling clinical data, is required.

Knowledge, Skills and Abilities:
• Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
• Strong attention to detail and skill with numbers
• Good written and verbal communication skills
• Good analytical/problem-solving skills
• Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
• Strong customer focus and excellent interpersonal skills.
• Proven flexibility and adaptability
• Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands
• Knowledge of medical/clinical terminology
• Understands project protocol and DVM
• Proven ability in achieving applicable technical competencies per the DM competency grid


Working Conditions and Environment:

• Work is performed in an office environment with exposure to electrical office equipment.

• Hybrid Work Arrangement (2x a week in the office)

• Occasional drives to site locations

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.