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Proclinical are recruiting a Clinical Research Associate for a pharmaceutical organisation. This role is on a permanent basis and is located in Belgium.
Responsibilities:
- Collaborate with sites to adapt, drive, and track subject recruitment plan aligned with project requirements to develop predictability.
- Review the quality and integrity of the study site practices linked to the suitable performance of the protocol and adherence to suitable guidelines.
- You will work alongside and mediate with the study team members for project implementation assistance when suitable.
- To handle ongoing project expectations and concerns, you will administer protocol and linked study training to allocated sites and form routine lines of communication with sites.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to an advanced degree in a scientific or healthcare field.
- Computer literacy.
- Communication skills both verbally and in writing.
- Fluency in the English, Dutch and French languages.
- Expertise and ability to execute suitable clinical research regulatory needs, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) regulations).
- At least 2 years of experience in on-site monitoring.
If you are having difficulty in applying or if you have any questions, please contact Auxanne Rameix at +44 203 954 7011.
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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