Jobs in Palermo, Italien
Progettista Elettronico Hardware Settore Elettronico Aerospazio Difesa TLC Engineering
JR Italy
Vernetze dich mit Headhuntern, um dich auf ähnliche Jobs zu bewerbenResponsabile delle Offerte per Impianti Fotovoltaici
JR Italy
Consulente del Credito - Agenti e Collaboratori
JR Italy
Addetto o Addetta Telemarketing Junior in Smartworking Part Time
JR Italy
Business Development Manager – Responsabile Vendite
JR Italy
Clinical Research Associate FREELANCE
Zusammenfassung
A Clinical Research Organization is seeking a Clinical Research Associate to join their Operational Italian Team. This remote position requires an individual with a technical-scientific degree and proven experience in clinical monitoring. Duties include conducting site visits, writing monitoring reports, and ensuring data integrity. Travel in Central-South Italy is required. A dynamic, multicultural work environment is offered.
Leistungen
Qualifikationen
- Bachelor’s degree/MD or equivalent in a technical-scientific field.
- Proved experience in clinical monitoring and trainings in the field.
- Proven GCP-ICH training.
- Actual CRA certification as per MoH decree 15/11/2011.
- Excellent organizational and time management skills.
Aufgaben
- Conduct and perform SQV/Pre-study Visits, monitoring visits, and close out visits.
- Write Monitoring Reports and perform site management activities.
- Check data integrity.
- Support the team on ethics committees submissions.
Social network you want to login/join with:
col-narrow-left
Evidilya
Other
-
Yes
col-narrow-right
8662617666420211712337141
3
27.08.2025
11.10.2025
col-wide
Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:
Clinical Research Associate
To reinforce the Operational Italian Team
Main Responsibilities:
- Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close out visits, according to SOPs and study Monitoring Plan
- Write Monitoring Reports and performing site management, addressing FU activities
- Check data integrity
- Support the team on the submission of the study to ethics committees/IRBs
Hard & Soft Skills:
- Bachelor’s degree/MD or equivalent in technical-scientific field
- Proved experience in clinical monitoring and proven trainings in the field
- Proven GCP-ICH training
- Actual CRA certification as per MoH decree 15/11/2011
- Excellent organizational and time management skills.
Additional requirements:
- Availability to travel especially in Central-South Italy
What we offer:
- Full remote job
- Multicultural, young and dynamic work environment
* Der Gehaltsbenchmark wird auf Basis der Zielgehälter bei führenden Unternehmen in der jeweiligen Branche ermittelt und dient Premium-Nutzer:innen als Richtlinie zur Bewertung offener Positionen und als Orientierungshilfe bei Gehaltsverhandlungen. Der Gehaltsbenchmark wird nicht direkt vom Unternehmen angegeben. Er kann deutlich über bzw. unter diesem Wert liegen.
einen besseren Job
Folge uns
