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The Clinical Data Management Associate supports the Clinical Data Management (CDM) team in providing high-quality data solutions that meet regulatory and client needs. You may also undertake leadership activities under the supervision of a Data Operations Coordinator (DOC) or Data Team Lead (DTL).
Key Responsibilities
- Serve as Data Operations Coordinator (DOC) for assigned clinical protocols or central laboratory studies.
- Conduct data review and resolve data clarifications.
- Lead database audit teams and ensure regulatory compliance.
- Assist in database development, testing, and edit specification creation.
- Perform clinical data coding and quality assurance checks.
- Ensure adherence to SOPs, GxP standards, and Good Clinical Data Management Practices (GCDMP).
- Maintain effective collaboration with global CDM teams and clients.
Qualifications & Skills
- Bachelor’s degree in Clinical, Biological, Mathematical Sciences, Pharmacy, or related discipline.
- Exposure to medical terminology and clinical data systems.
- Strong analytical, organizational, and problem-solving skills.
- Excellent communication, leadership, and computer proficiency.
- Ability to work independently and collaboratively in a fast-paced environment.
Why Join IQVIA?
- Work with a global leader in clinical research and healthcare analytics.
- Gain exposure to cutting-edge data management systems and global clinical trials.
- Opportunity for career growth and continuous learning through IQVIA’s training programs.
- Collaborative, inclusive, and innovation-driven work culture.
How to Apply
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