Clinical Research Associate

Proclinical are recruiting a Clinical Research Associate for a CRO.

This role is on a permanent basis and is located in Melle with the ability to work remotely from home.

The client is focused on performing clinical trials is crucial to success.

Responsibilities:

• Contribute to divisionwide duties to partake in the optimisation of procedures within the division.
• Serve as the main point of contact for communication between sponsor, site personnel and any thirdparty.
• Operate rendering to the suitable quality management system for the company or a client.
• Guarantee that sites are prepares and prompt to perform the study linking to training, study supplies, medication amongst other, etc.
• You will arrange communications between site personnel and any other party.
• Conduct proposals to the ethical committees and regulatory authorities such as initial submissions, notifications, amendments and safety information amongst other.
• Form and uphold good cooperation with investigators and site personnel.
• Other duties may be assigned to this role.

Key Skills and Requirements:

• Educated to a degree level in a life science.
• At least a year of experience in a global clinical research organisation.
• Fluency in the English, Dutch and French with knowledge in another European language would be beneficial.
• Expertise on ICH-GCP and all suitable regulatory needs.
• A diplomatic and methodical individual who works well in a team as well as independently.
• Communication skills both verbally and in writing.
• Able to resolve issues.
• An organised individual who is precise and possess analytical skills.
• A high attention to detail.
• Resistant to stress.
• Willing to travel for business needs.

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-AA2

Clinical

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