Services
Project Management
Regulatory:
Submissions to authorities and Ethics Committees in various countries: Belgium, the Netherlands, UK, France
Clinical Trial Monitoring for phase I – IV clinical trials:
starting from prestudy visit until study close out.
Clinical Trial Management:
collection of essential/critical documents, reporting and handling safety information, experience with electronic CRFs, drug handling and accountability.
Administrative tasks: writing visit reports, creating newsletters, translations of informed consents (Dutch and English), patient questionnaires and other site and patient specific documents.
Organisations of investigator meetings
Feasibilities
Set up CRFs, design and production of didactic material (e.g. investigator Pocket cards, schedule of assessments, patient cards)
Training
Clinitude is hiring!
Do you have what it takes to work at Clinitude? We are passionate about Clinical trials. Because we continually strive to define our standing as experts in the clinical research industry, Clinitude seeks reliable and enthusiastic team members to help lead the company. more information