Job Description

Location: Barranquilla
Hours: Monday to Friday, 7:30 a.m. – 4:30 p.m.

An important institution in the health sector is looking for a Clinical Studies Coordinator.

Requirements:

Professional in health or related areas.
2 to 3 years experience in clinical research.
Advanced level of English (C1), essential.
Residing in Barranquilla.

Main functions:

Provide support in the preparation and execution of clinical research studies.
Review study protocols, case report forms (CRF) and other associated documentation.
Manage electronic data capture systems.
Participate in meetings related to studies.
Compile and submit regulatory and ethics documentation in accordance with guidelines from the FDA and other regulatory entities.
Recruit and select patients for clinical trials, maintaining updated records.
Orient participants to the study, including objectives, procedures, and timelines.
Design and maintain source documentation in accordance with protocol requirements.

We offer:

Job stability.
Opportunity for professional growth.
Link with a team specialized in clinical research.

If you meet the profile, we invite you to apply.",