Research Project Coordinator

hace 2 días


Barcelona, Barcelona, España Vhir A tiempo completo

**Company Overview**

The Nephrology and Kidney Transplantation Research Group at the Vall d'Hebron Research Institute (VHIR) is a renowned research institution based in Barcelona, Spain. As a leading public center for Catalunya and many other areas of Spain, we provide multidisciplinary care involving all pediatric and adult medical and surgical sub-specialties.

We work closely with the Pediatric Urology Service, accredited as a national reference service for complex urologic surgeries in children and adolescents. Our research focuses on Inherited Tubulopathies (Dent disease, Familial hypomagnesemia with hypercalciuria nephrocalcinosis) and rare kidney diseases. We are committed to developing new therapies in pediatric patients and participate in several international clinical trials and academic research projects focused on chronic kidney disease in children and rare kidney diseases.

Salary: The estimated salary for this position is between €35,000 and €50,000 per annum, depending on experience.

Job Description:

We are seeking an experienced Research Project Coordinator to join our team. The successful candidate will be responsible for coordinating clinical trials to ensure compliance with the protocol. This includes providing information to potential participants, conducting and supervising tasks related to clinical trials and research projects, and coordinating with different vendors.

Required Skills and Qualifications:

* Bachelor's Degree in Pharmacy and Master in Clinical Trials* At least 4 years of experience working in clinical trials* At least 4 years of experience in pediatric hospital environments* Computer literacy (Office package, mail, eCRF)* Fluency in Catalan, Spanish, and English (business level)

Main Responsibilities and Duties:

  1. Provide information to potential participants in clinical trials.
  2. Conduct and supervise tasks related to clinical trials and research projects.
  3. Coordinate with different vendors: sample and medication couriers, digital patient platforms (questionnaires, diaries...), IVRS, payment platforms, home nurses, medical imaging platforms, sample and imaging central laboratories, trial management platforms.
  4. Report to Pharmacovigilance: notify and explain the SAEs and follow up on them.
  5. Submit applications to the Clinical Research Ethics Committee (CEIm) for research projects.
  6. Select, include, and follow up with patients in clinical trials.
  7. Handle biological samples: centrifugation, freezing, shipping to central laboratories, etc.
  8. Maintain up-to-date clinical data from source documents in eCRFs, CTMS, and ISF.
  9. Attend site-monitoring visits, review, and resolve queries in accordance with GCP.


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