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Clinical Research Associate - Multisponsor Team

iqvia · Bucuresti

New
Hybrid Junior 🇬🇧 English
ICH-GCP CTMS eTMF EDC

Job description

About the role

iQVIA is looking for a Clinical Research Associate to support its multisponsor team in Romania. The role covers the full spectrum of clinical trial site activities, from patient recruitment to study close-out, and involves collaboration with the project and study team.

Key responsibilities

  • Perform visits such as selection, initiation, monitoring and close-out in line with ICH-GCP guidelines.
  • Support the site(s) in patient recruitment.
  • Manage RCA and CAPA.
  • Report visits and study progress.
  • Manage and archive study documents in eTMF.
  • Collaborate with the project and study team.
  • Document findings in Monitoring Visit Reports and follow-up letters.

Required profile

  • MSc and/or BSc degree; Health Sciences preferred.
  • Proficiency in Romanian and English.
  • Based in Romania, with availability to travel across the country and a driving licence.
  • At least 1 year of experience as a CRA.
  • Experience across different studies, phases, visits and therapeutic indications.
  • Passion for science, helping patients and working with sites.

Required skills

  • Good knowledge and application of ICH-GCP.
  • Use of CTMS, eTMF and EDC systems.

What we offer

  • Work on international projects with one of the top 5 sponsors globally, focusing on quality and with a stable workload.
  • Career development opportunities.
  • Flexible conditions and an attractive remuneration package.
  • Hybrid model, with office-based and home-based roles available.

Questions fréquentes

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Source : ats:workday

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Published 3 hours ago

Expires 1 month from now

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iqvia

Bucuresti