Clinical Research Assistant — Multicenter Trials

Pepr-Propsy; Paris; Híbrido; EUR 32.000 - 42.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Continuing education in clinical研究

National PEPR project exposure

Access to PEPR events & training

Descripción de la vacante

The Fernand Widal hospital is recruiting a clinical research assistant to ensure rigorous data collection, coordinate inclusion and follow-up visits, and liaise with eCRF and teleconsultation platforms. This position plays a key role in data quality, protocol compliance, and the smooth patient journey, with duties spanning study visit coordination, data entry, and platform interfacing.

Applicants should hold a bachelor’s or master’s in clinical research; experience in multicenter trials or

Formación

• Bachelor’s or Master’s degree in clinical research or equivalent.
• Experience in multicenter clinical trials or real-world data (RWD) studies.
• Proficiency in eCRF tools (e.g., Viedoc, CleanWeb, REDCap, etc.).
• Knowledge of clinical research regulations (Jardé, CNIL, BPC, etc.).
• Proficiency in office software and electronic document management systems.

Responsabilidades

• Coordination of study visits: logistics and scheduling of inclusion, follow-up, and end-of-study visits.
• Data collection and entry: input of clinical data into eCRF and French Minds platform; ensure completeness and quality.
• Interface with platforms: create patients in eCRF and Minds environments; coordinate workflow with calendar system.
• Quality and compliance: follow protocol/SOPs; participate in audits, monitoring, and quality control; address deviations.
• Communication and follow-up: weekly meetings with PEPR teams; share information with clinical/research team; liaise with coordination units.

Conocimientos

Clinical research degree

Multicenter trials / real-world data

eCRF tools (Viedoc, REDCap)

Clinical research regulations (Jardé,

Educación

Bachelor’s/Master’s in clinical research

Herramientas

eCRF tools: Viedoc, CleanWeb, REDCap

Descripción del empleo

The Fernand Widal hospital is recruiting a clinical research assistant to ensure rigorous data collection, coordinate inclusion and follow-up visits, and liaise with eCRF and teleconsultation platforms. This position plays a key role in data quality, protocol compliance, and the smooth patient journey, with duties spanning study visit coordination, data entry, and platform interfacing.

Applicants should hold a bachelor’s or master’s in clinical research; experience in multicenter trials or