CRA pharma company in Utrecht 32-40 uur office/home based
For one of our CRO clients we are looking for a client deadicated CRA in the Utrecht region.
Working for the pharmaceutical company you perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and company SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation Responsible for ensuring that data will pass international quality assurance audits. Represents the company in the global medical research community and develops and maintains collaborative relationships with investigational sites. Required to travel 60-80% on average. Most monitoring sites are in the south/middle of the Netherlands.
Responsibilities for the function as a Clinical Research Associate:
- Bachelor’s degree or licensed certified health care training or equivalent combination of education and experience;
- At least 1 year of clinical research experience in all phases of study life cycle, including start up, interim and close out;
- Equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities;
- Valid Driver’s License.
You will receive a competative salary with good secundairy benefitsm personal development and training programs.
More information about the CRA Pharma? Please reach out to the recruiter on the right handside or apply via the button.