We are currently recruiting for an experienced CRA/SCRA to join our growing organisation. This is an excellent opportunity to join a Growing CRO. You will have the opportunity to move into a LCRA/ Lead clinical research associate - Clinical Project Manager role as we are an organisation that mostly focuses on internal promotions.
We are an International CRO, globally recognised and respected. We focus on providing a full service to our Clients that include Pharmaceutical, biotechnology and medical device organisations.
Performs and coordinate all aspects of the clinical monitoring and site management
Conducts site visits - assessing protocol and regulatory compliance, managing required documentation.
Develops and maintaining collaborative relationships with investigational sites and client company personnel.
Assisting on assigned projects and will take a lead role where required.
Mentor, train and contribute to the development of junior clinical research assistants.
Suitable for: CRA, Clinical research associate, CRA II, CRAII, Clinical research associate II, SCRA, Senior CRA, CRA III, CRAIII, Clinical research associate III, Lead CRA with:
2 years + monitoring experience
Good knowledge of ICH-GCP and relevant regulations
Motivation to progress in a growing company
Excellent communication skills
Strong attention to detail
Fluent in English and Dutch
Full job description and company details are available upon enquiry. Please call Nick on +44 (0) 203 019 6013 or email directly at firstname.lastname@example.org for further details about this opportunity - This will be 100% confidential.