Our client, one of the largest contract research organisations in the world, provides a broad range of services to the biopharmaceutical, and medical device industries. They are seeking Clinical Study Start Up Specialists (all levels) for the Netherlands.
The Clinical Study Start Up Specialist will conduct and facilitate specific start-up activities, including site identification, feasibilities, essential document collection and review, ICF customization, EC submissions, preparation and negotiation of Clinical Site Contracts. This post has a high accountability on quality and timelines.
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Degree in a health related discipline including nursing or other relevant qualification
Clinical trials experience
Understanding of GCP and relevant regulations
Previous experience in Study Start up is required
PERSONAL SKILLS & ATTRIBUTES:
Good team working skills
Strong interpersonal skills
Good computer skills
BENEFITS OF THE ROLE: This premier contract research organisation has the reputation of offering the broadest possible range of opportunities in the pharmaceutical industry. They offer competitive salaries, excellent learning and development opportunities and comprehensive benefits.
Fforde is acting as a recruitment agency/business.
KEY WORDS: Study Start Up Specialist, Site, Clinical, Clinical Research, Clinical Trial, Clinical Study, Degree, health, Medicine, Nurse, Pharmaceutical, CRO, Netherlands, Europe