On behalf of our client, a leading healthcare organization, we are
seeking a meticulous Clinical Data Coordinator to manage and oversee
clinical trial data collection, validation, and reporting. This role is crucial
in ensuring data integrity and regulatory compliance in their research
initiatives.
Responsibilities:
- ✓ Design and implement data collection protocols for clinical studies
- ✓ Monitor data quality and perform regular database audits
- ✓ Coordinate with clinical sites to ensure timely and accurate data
submission
- ✓ Prepare clinical study reports and regulatory submissions
- ✓ Maintain electronic data capture (EDC) systems and databases
- ✓ Train clinical staff on data collection procedures and GCP
guidelines
- ✓ Support regulatory inspections and audit preparations
Requirements:
- ✓ Bachelor's degree in Life Sciences, Nursing, or related healthcare
field
- ✓ 3-4 years of clinical research or data management experience
- ✓ Knowledge of GCP, FDA regulations, and clinical trial processes
- ✓ Proficiency in EDC systems (Medidata Rave, REDCap, or similar)
- ✓ Strong attention to detail and analytical skills
- ✓ CCDM or ACRP certification preferred
- ✓ Experience with statistical software (SAS, SPSS) is a plus
Job Location
+2547 98 431 116