Clinical Research Data Specialist
3 weeks ago
Overview
Be a part of our fast-growing team and unchain all the possibilities. We are looking for a Clinical Research Data Specialist to support accurate and compliant data management in clinical trials. You will handle study protocols, perform data validation, monitor accuracy, and conduct quality assurance checks to ensure integrity of clinical research data. This role requires prior experience in clinical trial data management, familiarity with medical terminology, and strong attention to detail to support high-quality research outcomes.
Responsibilities- Understand and comply with study protocols and quality assurance measures for accurate data collection.
- Accurately track study timepoints to meet research objectives on schedule.
- Conduct internal audits on data completeness, validity, and accuracy.
- Perform data validation checks, identifying missing entries and discrepancies.
- Validate and test newly created forms before deployment in the database.
- Conduct UAT (User Acceptance Testing) on new registries and platforms before launch.
- Input tester data to enable project validation.
- Collaborate with research teams to ensure data integrity and compliance with study protocols.
- Perform other related duties as assigned.
- 1–2 years of experience in clinical trial data management (MUST).
- Background as a Medical Coder or with related data coordination/data management experience.
- Familiarity with medical terminology.
- Knowledge or exposure to PHI security and HIPAA compliance.
- Strong attention to detail and accuracy.
- Ability to work with cross-functional research teams.
- Organized, proactive, and able to work under strict timelines.
- Above-industry salary package and incentives.
- Comprehensive HMO benefits and life insurance from day 1.
- Free learning and development courses for your personal and career growth.
- Dynamic company events.
- Opportunities for promotion.
- Free meals and snacks.
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