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 prospect 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 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 and relevant formal academic / vocational
qualification
• Previous experience that provides the knowledge, skills, and abilities to
perform the job (comparable to 3 to 7 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 A
📌 Senior CDA/ Clin Data Assoc II (Bengaluru)
🏢 Thermo Fisher Scientific
📍 Bengaluru
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