Here at Syneos Health
we are currently recruiting for a Clinical Trial Associate for an office based sponsor-dedicated role in Lucerne in Switzerland.
Your main responsibilities :
Track (e.g. essential documents) and report (e.g. Safety Reports)
Ensure collation and distribution of study tools and documents
Update clinical trial databases (CTMS) and tracker
Collate, distribute / ship, and archive clinical documents, e.g. eTMF
Assist with eTMF reconciliation
Provide to and collect from investigators forms / lists for site evaluation / validation, site start-up and submissions
Support preparation of submission package for IRB / ERC and support regulatory agencies submissions.
Develop, control, update and close-out country and site budgets (including Split site budget)
Calculate and execute payments (to investigators, vendors, grants)
The ideal candidate will need the following experience / skills to be considered :
First experience in Clinical Research or relevant healthcare experience will be preferred.
Fluent in German and English language (verbal and written)
Good knowledge of French language is required
Good computer skills
Effective time management, organizational and interpersonal skills
Ability to set priorities and handle multiple tasks
We have a comprehensive benefits package and offer highly competitive remuneration.