Attiva gli avvisi di lavoro via e-mail!

Clinical Research Associate FREELANCE

Evidilya

Bari

Remoto

EUR 30.000 - 45.000

Tempo pieno

Ieri
Candidati tra i primi

Descrizione del lavoro

A clinical research organization is seeking a Clinical Research Associate to join their team. This remote position involves conducting site visits, monitoring trials, and ensuring data integrity. Candidates should have a relevant degree and experience in clinical monitoring, along with fluent English and excellent organizational skills. Travel in Central-South Italy is also required.

Servizi

Full remote job
Multicultural work environment

Competenze

  • Experience in clinical monitoring and trainings in the field.
  • GCP-ICH certification required.
  • CRA certification per MoH decree 15/11/2011.

Mansioni

  • Conduct SQV / Pre-study Visits, monitoring visits, close out visits.
  • Handle remote data monitoring using EDC systems.
  • Write Monitoring Reports and perform site management.

Conoscenze

Clinical monitoring experience
English fluency
Organizational skills
Time management

Formazione

Bachelor's degree / MD or equivalent
Descrizione del lavoro
Overview

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

Responsibilities
  • Conduct and perform SQV / Pre-study Visits, site initiation visits, monitoring visits, close out visits, according to SOPs and study Monitoring Plan
  • Handle remote data monitoring using validated EDC system / software
  • Write Monitoring Reports and performing site management, addressing FU activities
  • Source Data Verification (SDV / eSDV)
  • 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
  • Fluent in English
  • 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
Ottieni la revisione del curriculum gratis e riservata.
oppure trascina qui un file PDF, DOC, DOCX, ODT o PAGES di non oltre 5 MB.