- Clinical Research Associate II, CRA II, Netherlands
COVANCE - one of the top 5 global Contract Research Organizations in currently looking for its next home based Clinical Research Associate II to join its local team in Netherlands. As a CRA II you will be responsible for all aspects of study site monitoring activities including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaise with vendors and other duties, as assigned. Oncology experience will be a plus!
- Senior CRA The Netherlands Home Base Oncology 80%-90%-100%
Entrust Clinical People are currently resourcing for an experienced Senior CRA The Netherlands Home Base Oncology (immediately available) with full clinical trial cycle experience. This position offers the flexibility of home based working and being dedicated to one Sponsor
- CRA / CRA II - Netherlands
Key People are looking for CRAs to work for our global CRO client in the Netherlands to be insourced to a leading pharmaceutical client.
Successful candidates will with more than 2 years experience will be able to work Home-Based.
Applicants MUST speak fluent Dutch and English
- Principal CRA – Leading Global Pharmaceutical firm – Netherlands
A cutting edge pharmaceutical company specialising in CNS are in pursuit of a Principal Clinical Research Associate to join their broad and diverse organisation. This large pharmaceutical prides itself on its commitment to the discovery and development of ground-breaking drugs that improve function and change the course of disease in patients with CNS related disorders.
- IN HOUSE CLINICAL RESEARCH ASSOCIATE (IH CRA) - Utrecht, Netherlands
An outstanding opportunity to join one of the world’s leading contract research organisations and be part of a dynamic and growing international company. Join PRA Health Sciences as an In House Clinical Research Associate and help realize your career potential.
- CRA II - Oncology - Netherlands
Completes project activities associated with monitoring functions of Phase I-IV clinical research studies while continuing to develop a solid understanding of the drug development process, Good Clinical Practices (GCP), and relevant regulations.
- Senior Clinical Research Associate - Leading American based pharmaceutical firm - Netherlands
My client, an American based pharmaceutical firm are currently seeking an experienced Senior CRA to join their office within the Netherlands who is able to speak either Japanese or Korean. Specialists within the field of Neurology this company have some very exciting expansion planned for the year ahead and are able to offer the successful candidate the chance to develop into a much more senior level position.
- CRA II
A global contract research organisation have an exciting opening for a CRA with solid monitoring experience to be home or office based in the Netherlands. The company specialises in research into pharmaceuticals, healthcare and nutrition and offer flexible conditions and excellent career development opportunities.
The Clinical Research Associate (CRA) will primarily be responsible for running phase II clinical trials for designated therapies. ...
- Senior Clinical Project Manager – Leading Medical device firm – Netherlands
A very rare opportunity has come up for a self-motivated and career driven individual with prior medical device experience to join my client as a senior clinical project manager. This position would see you working on a number of different device studies as well as driving the company forward and assisting with their European growth.
- CRA/Senior CRA – Home or office based for a leading global pharmaceutical firm in the Benelux
My client, a market leading global pharmaceutical firm currently have an opening for an experienced and self-motivated individual to join them on their late phase clinical studies. As a CRA working within the clinical operations team you will be at the forefront of clinical trials practice. You will be involved in Implementing and monitoring trials, ensuring that sponsor and investigator obligations are met and overseeing compliance with regulatory requirements.