Senior Clinical Trial Assistant - Switzerland - Office Based in Lucerne - Permanent Contract
Clintec is currently looking to hire a Senior CTA to join our sponsor office based team in Lucerne, Switzerland. The position is on a full time, permanent basis. Apply now to become part of our global organisation.
Due to a period of sustained expansion, several outstanding career opportunities have arisen within Clintec, a truly unique CRO, for talented Clinical Trial Assistants to join our experienced team in Switzerland.
Responsibilities of the SrCTA:
Ensure administrative work of clinical trials: Create Investigator Files and other study information, booklets, worksheets, etc
Ensure timely translation and validation process of study materials (e.g. patient diaries, instructions, IC).
Provide investigators with all forms and lists to start the site evaluation and site validation (initiation and start of study information).
Archiving of processes, including electronic SORF and Trial Master File.
Ensure timely ordering of study tools.
Preparation of ethical and regulatory submissions.
Ensure protocol initiation processes.
Organization and documentation of regular study meetings.
Organization and documentation of local investigators meetings.
Provide professional presentation of study materials for CRA and investigator trainings.
High School Degree or equivalent.
Previous experience in a similar role would be highly advantageous.
Good knowledge of the clinical trial process.
Fluency in German, English & French (written and spoken)
Strong organisational and communication skills.
Willing and able to work office-based in Lucerne, Swizterland
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.