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Work Schedule
Second Shift (Afternoons)Environmental Conditions
OfficeJob 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.
