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Proclinical are recruiting for a CRA, Belgium for a CRO. This role is on a permanent basis with the ability to work remotely from anywhere in Belgium.
Key Responsibilities:
- Perform study drug inventory, as well as adverse event and serious adverse event reporting and follow-up.
- Examine patient recruitment and retention.
- Conduct source document verification and case report from evaluation, as well as regulatory document evaluation.
- You will perform pre-study, initiation, supervision and closeout visits for research sites.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to a degree level in a health-connected discipline.
- Familiarity in a CRA role with at least 2 years of experience.
- Expertise on medical vocabulary and clinical patient management.
- Know-how of drug therapy practices and clinical research strategies.
If you are having difficulty in applying or if you have any questions, please contact Grace Koko at g.koko@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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