Clinical Trial Coordinator - Switzerland – Office Based, Lucerne - Permanent
Clintec is actively recruiting for a Clinical Trial Coordinator (Assistant) to join our growing team in Switzerland. This is a permanent opportunity, outsourced to our major sponsor working from their office in Lucerne.
Responsibilities of the Clinical Trial Coordinator:
Tracking and reporting trial documents and ensuring collation and distribution of study tools and documents
Updating clinical trial databases
Management of clinical and non-clinical
Prepare, collate, distribute and archive clinical documents and correspondence
Updating manuals/documents (e.g., patient diaries, instructions) and documenting proper destruction of clinical supplies
Providing and collecting from investigators forms/lists for site evaluation/validation and site start-up
Preparation of submission package for IRB/ERC and support regulatory agencies submissions
Collaboration with finance/budgeting representatives for tracking, reporting of negotiations, contract development, approval, maintenance and payments (investigators, vendors, grants)
Monitor, track adherence and disclosures and budget closeout
Organising meetings, creating and tracking study memos/letters
Supporting and preparing for local investigators meetings
High School Degree or equivalent.
Previous experience in a similar role would be highly advantageous.
Good knowledge of the clinical trial process.
Fluency in English, French, German and ideally Italian (both written and spoken).
Strong organisational and communication skills.
Willing and able to work office based in Lucerne
Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 50 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.
Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.