Clinical Trials Assistant Beschrijving: Clinical Trials Assistant - The Netherlands - Permanent or Contract - Immediate Start ClinTec International is actively recruiting for a Clinical Trials Assistant to join our expanding global company in The Netherlands - this is a Permanent or Contract office based opportunity in Woerden. By working for ClinTec you can further your career in a dynamic, fast-paced environment and you can be assured of rewarding benefits. 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 lifecycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world’s leading pharmaceutical companies and CRA’s can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. ClinTec International offers a competitive salary and rewards package. Role Description Responsibilities of the Clinical Trials Assistant • 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). • 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. • Archiving of processes, including electronic SORF and Trial Master File. |