Description
IQVIA is looking for a Clinical Research Associate to provide service to the multisponsor team.
You will be responsible for:
- Performing visits (such as selection, initiation, monitoring and close-out) according to ICH-GCP guidelines.
- Support of the site(s) in relation to patient recruitment.
- RCA and CAPA management.
- Reporting of visits and progress of the studies.
- Management and archiving of study documents in eTMF.
- Collaboration with the project/study team.
- Documentation in Monitoring Visit Reports and follow-up letters.
We are looking for:
- MSc and/or BSc education level, preferably in Health Sciences.
- Proficient level of Romanian and English.
- Good knowledge and application of ICH-GCP.
- Minimum of 1 year of experience as a CRA.
- Experience in using CTMS, eTMF and EDC systems.
- Experience in different studies, phases, visits and therapeutic indications.
- Passion for science, helping patients and collaborating with the sites.
- Availability to travel across the country, driving license.
What we offer:
- Working with one of the TOP 5 sponsors globally on international projects.
- Focus on quality, not quantity.
- The chance to work on cutting-edge medicines right at the forefront of drug development.
- Genuine career development opportunities.
- Flexible conditions and an attractive remuneration package.
- Hybrid model, office-based and home-based roles available.