Clinical Research Associate (M / F / D)
Tasks :
* Act as the primary contact between sponsor and investigative sites for the conduct of a clinical study in Spain.
* Oversee recruitment of patients across 3 study sites (Catalonia, Santiago de Compostela, Valencia).
* Ensure that informed consent is obtained in accordance with GCP and local regulations.
* Monitor and coordinate scheduled blood draws per patient (first at the hospital, second at the patient’s home).
* Conduct regular on-site and remote monitoring visits to verify data accuracy, source documentation, and protocol compliance.
* Provide guidance and support to site staff regarding study procedures and documentation.
* Track recruitment progress and prepare monitoring reports.
* Address and resolve site-related issues to ensure smooth study conduct.
Qualification :
* Degree in life sciences, nursing, pharmacy, or a related field.
* Proven experience as a CRA in non-interventional clinical studies.
* Knowledge of Good Clinical Practice (GCP), ICH guidelines, and Spanish regulatory requirements.
* Strong organizational and communication skills.
* Ability to work independently and manage multiple priorities.
Requirements :
* Start : September
* Duration : ~ 12 months
* Capacity : Approx. 0.25 FTE
* Location : Spain (Catalonia, Santiago de Compostela, Valencia) with potential for remote work between visits
#J-18808-Ljbffr