Clinical Research Associate
Job Clinical Research Associate
In the final phase of Synthon’s generic drug development program the Clinical Research and Development department conducts clinical trials to demonstrate bioavailability and bioequivalence of our medicines. The clinical research associate (CRA) will be involved in designing the studies and will be responsible for initiating and managing clinical trials for regulatory purposes. This includes close collaboration with international clinical research organizations (CROs) to draw up protocols and reviewing these protocols to verify compliance with good clinical practice (GCP) and with regulatory requirements. The CRA will coordinate and monitor the clinical studies in accordance with GCP. Upon completion of the studies, the CRA will review the documentation to verify compliance with GCP and with regulatory requirements. International travel is part of the job, generally during a few days once or twice a month. The CRA reports to the vice president of Clinical Research and Development.
Profile Clinical Research Associate
Your letter of motivation and CV should show that you have:
- A master’s degree in either clinical scientific research, biomedical sciences, pharmaceutical sciences or equivalent.
- Preferably two years of working experience in a business environment.
- A good command of the English language, in speaking and writing.
Experience in coordinating clinical studies is an advantage.
In interviews you will be able to demonstrate that:
You have an analytical mind and are capable of keeping a good overview of your work. You have excellent planning and organizational skills. You are a good communicator: you are able to clearly explain to external parties what needs to be done and what you expect. You are expected to keep all parties involved well-informed and updated. Your approach to work is pragmatic and structured, but you are also open-minded and flexible when required.
Contract hours: 32-40 hours.
Salary: scale 14.
Please send your application before January 30th 2018. The first round of interviews will take place on February 5th and 6th 2018 and the second round of interviews will be on February 12th 2018.
For further information please contact Sandra van Os, VP Clinical R&D at tel. +31 (0)24 - 372 77 00. If you are interested in this challenging position, we look forward to your application. You can apply via the apply button / link, which will directly lead you to our website.
Recruitment by commercial agencies in relation to this vacancy is not appreciated.