Within this role you will assume administrative and trial support responsibility for ongoing Clinical Trials and you will undertake Trial Management activities as directed by Clinical Project Managers.
Your primary responsibilities will includes the coordination and support of study and data management activities to ensure the standardisation and consistency of delivery across studies in accordance with protocol, standard processes, procedures, meets quality & timeline metrics and GCP/ICH requirements.
You will also track and maintain study information and report on study progress and advises on the availability of standardized tracking tools and templates. You also ensure efficient communication and follows-up on study specific action plans for resolution
Located in the heart of one of the most beautiful parts of Switzerland with one of the highest standards of living and quality of life this organisation is committed to improving the lives of people across the world and dedicated towards implementing innovative solutions highlighted by their exciting pipeline and strong portfolio of products
Suitable candidates will be able to demonstrate previous experience working as a Clinical Trial Coordinator and will be able to work office based.
You will be given a balanced mix of sufficient responsibility with adequate resources which will allow you to make a real difference whilst simultaneously being recognised and rewarded for your efforts.
If you are interested in this new, exclusive career opportunity, please email your application to louis.gicquel@secpharma.com or call Louis Gicquel on +44 207 255 6600.
SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business