$ads={1}
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:
- Guarantee efficient communication between the investigational sites and internal/external shareholders.
- When needed, you will operate on project work and initiatives for process improvement.
- Supervise various sites, which involves RMB on an independent basis.
- Contribute to investigator meeting when required.
- Guarantee that the trial is performed rendering to the approved protocol ICH-GCP regulations, SOPs etc.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to a degree level in a pharmacy, life science or similar discipline.
- At least 1- 3 years of experience in a pharmaceutical, biotech or CRO would be ideal.
- At least 1 years of experience in a clinical supervisory role on an independent basis.
- Comprehension and exhibited implementation of GCPs and suitable SOPs.
- Acquaintance with oncology trials.
- Fluency in the English, French and Dutch languages.
- Comprehension of medical/therapeutic area knowledge and medical vocabulary.
- Able to handle regulatory and/or IEC queries.
- Capable of developing and preparing local notified consent forms.
- Communication skills both verbally and in writing.
- Ability to handle the delivery of study providers.
- Customer oriented individual with interpersonal abilities.
- A high attention to detail.
- An organised individual with the ability to manage time efficiently.
- A flexible and adaptable individual with the ability to work well both in a team as well as independently.
- Computer literacy.
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.
#LI-GK1
#ClinicalResearch