Clinical Research Site Coordinator & TMF Specialist

Psicro; Argentina; Presencial; ARS 600.000 - 1.000.000; Jornada completa

Descripción de la vacante

Psicro is seeking a proactive, detail‑oriented clinical research support specialist to streamline communication, maintain systems, and manage documents for international projects.

You will be the main site contact for CRA queries, coordinate TMF and ISF activities, ensure regulatory submissions, and support site training and vendor coordination. Fluency in English and experience in clinical research are required.

Formación

• College/University Degree in Life Sciences.
• Full working proficiency in English.
• Experience working as CTA for CROs and in Clinical Research.
• Knowledge of local regulations and CTMS/ISF processes.
• Ability to plan and work in a dynamic team environment.

Responsabilidades

• Being the main point of contact between site personnel and CRA; assist in query resolution and EDC completion.
• Serve as primary site contact for vendors, study supplies, and access management.
• Ensure pre-study testing of local site facilities is completed.
• Assist Monitors with subject/event data in CTMS and track issue resolution.
• Manage TMF, ISF files, and site/country level document handling and audits.
• Coordinate site training for vendor-related systems and translations status review.
• Ensure safety information flow with investigative sites.

Conocimientos

Communication skills

Teamwork

Planning

English proficiency

MS Office

Educación

College/University Degree in Life Sciences

Herramientas

MS Office

Descripción del empleo

Psicro is seeking a proactive, detail‑oriented clinical research support specialist to streamline communication, maintain systems, and manage documents for international projects.

You will be the main site contact for CRA queries, coordinate TMF and ISF activities, ensure regulatory submissions, and support site training and vendor coordination. Fluency in English and experience in clinical research are required.