Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
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:
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Supports the setup of study activities such as database design, testing of data entry screens, and Data Validation Manual (DVM) creation, as required.
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Reviews data listings for accuracy and consistency of data.
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Acts as point person and subject matter expert for specialized study-specific processes.
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Generates, tracks and resolves data clarifications and queries and makes changes to the clinical database as required.
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Contributes to the improvement of data management processes on a global level.
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Produces project-specific status reports for management and/or clients on a regular basis.
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Provides training and work direction to junior staff as required.
Education and Experience Requirements:
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Bachelor's degree or equivalent and relevant formal academic / vocational qualification
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Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2 to 4 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:
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Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
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Strong attention to detail and skill with numbers
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Good written and verbal communication skills
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Good analytical/problem-solving skills
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Ability to maintain a high degree of confidentiality with clinical data and client's proprietary data
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Strong customer focus and excellent interpersonal skills.
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Proven flexibility and adaptability
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Must be able to set and meet timelines or be able to negotiate schedule changes in response to project demands
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Knowledge of medical/clinical terminology
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Understands project protocol and DVM
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Proven ability in achieving applicable technical competencies per the DM competency grid
Working Conditions and Environment:
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Work is performed in an office environment with exposure to electrical office equipment.
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Occasional drives to site locations
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Occasional travel both domestic and international.
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.
