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:
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Good Clinical Practices (GCP)
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Standard Operating Procedures / Work Process Documents (SOPs/WPDs)
Your work will support the assessment of the safety and efficacy of investigational products and/or medical devices.
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Support the setup of study activities such as:
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Database design
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Testing of data entry screens
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Data Validation Manual (DVM) creation as required
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Review data listings for accuracy and consistency
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Generate, track, and resolve data clarifications and queries
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Make changes to the clinical database as required
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Act as point person and subject matter expert for specialized study-specific processes
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Contribute to the improvement of data management processes on a global level
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Understand project protocol and DVM requirements
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Produce project-specific status reports for management and/or clients on a regular basis
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Provide training and work direction to junior staff as required
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Collaborate with project teams while maintaining high quality standards
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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 0 to 2 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.
✅ Ability to apply knowledge and skills in a highly organized fashion while adhering to:
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Regulatory guidelines
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Global SOPs
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Client expectations
✅ Strong attention to detail and numerical skills
✅ Good written and verbal communication skills
✅ Good analytical and problem-solving skills
✅ Ability to maintain a high degree of confidentiality with clinical and proprietary client data
✅ Strong customer focus and excellent interpersonal skills
✅ Proven flexibility and adaptability
✅ Ability to set and meet timelines or negotiate schedule changes in response to project demands
✅ Knowledge of medical/clinical terminology
✅ Proven ability in achieving applicable technical competencies per the DM competency grid
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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
When you join Thermo Fisher Scientific, you become part of a global team that values:
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Passion
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Innovation
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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.
