RPS has now strongly developed its activities across Europe and due to our constant growth we are currently looking for a Data coordinator position part-time in the mornings (25 hours/week)
-Adhere with corporate internal polices and requirements and internal requirements of Sanofi.
- Work with different sites (all in Barcelona area) and studies, collaboration with full in the eCRF, TMF, work together with the CRA, between others
- Experience is not required but it will be appreciate some experience in similar task or post graduate studies related with monitoring task
- Ensure proper storage, dispensation and accountability of clinical supplies and study drug.
- Maintain adequate site tracking records
- Follow up of drug safety issues and safety reports in timely manner, if applicable
- Communicate site study issues, concerns, and progress to Project Manager, Clinical Team Lead, and Clinical Research Manager accordingly
- Assist with the implementation of corrective actions when appropriate
- Assist in data clarification process (incl. query process)
- Prepare /review all patients tracking records
- Input and maintain study information concerning subject status of financial reimbursement
The requirements are:
- Degree in Health Sciences
- Minimum 1 year of experience as Clinical Study Coordinator or Clinical Research Associate
- Strong familiarity with ICH-GCP directives and Quality Assurance procedures
- English and Spanish
- Availability to travel aroun Barcelona
