Clinical Research Associate - Multisponsor Team
iqvia · Bucuresti
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.
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iqvia
Bucuresti
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