Clinical Research Associate (CRA) - Croatia - Office Based

An exciting opportunity to work with a expanding Clinical Research Organisation with established global capabilities. The company is seeking high calibre Clinical Research Associates to work at an international level on trials within the Cardiovascular therapeutic area. As one of the most innovative and scientifically minded CROs this is an appealing opportunity, where you will be working in an adaptive environment in a highly-visible role.

Key Duties and Responsibilities:

* Contribute to study documents e.g. ICF and adjust to local requirements
* Identify, conduct feasibility and evaluate trial sites within the assigned geographical area. Manage and monitor sites from evaluation to close-out. Ensure sites comply with protocol, Good Clinical Practice and any other relevant guidelines.
* Manage clinical documentation including the TMF. Review trial data including CRF. Provide input to regulatory and ethical submissions.
* Work with Drug Safety in the case of SAEs and AEs
* Maintain a close working relationship with the Clinical Trial Manager and the Pharma / Biotech sponsor.
* Negotiate contracts and payment with the study site Investigators.
* Manage drug supplies.

Education and Skills:
* Appropriate qualification in Life Sciences, Nursing or Medical Degree.

* Working knowledge as a Clinical Research Associate (CRA) ESSENTIAL Candidates will be proficient in monitoring multi-site trials. International experience is highly desirable.

*A proven working knowledge within the Cardiovascular therapeutic area.

* Fluent in English and Croatian


Key Words: Clinical Research Associate CRA Senior Clinical Research Associate Permanent Office Based CRO Clinical Research Organisation Cardiovascular Cardiology Croatia Zagreb