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 division-wide 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 third-party.
- 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.

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