There is an exciting new opening for a German speaking Clinical Research Associate II to join a rapidly expanding CRO. This is a remote position that offers a competitive salary and the opportunity to develop your skills and career further.
They are leaders within the UK Clinical Research industry, specialising across a range of therapeutic areas. They have a proven track record of a reliable, cost-effective and high quality services that has created long-standing relationships with leading pharmaceutical and biotechnology organisations. This is a brilliant opportunity to join a specialist CRO, which encompasses their staff, clients and patients into their drug development process, striving to make a difference across the world.
The CRA Position
This is an opportunity to continue to develop your clinical skills and enhance the opportunity to progress your career. The key responsibilities are to identify, select, initiate and close-out investigational sites for a wide range of clinical trials.
Further responsibilities include –
Ensure all trials are reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.
Establishes, updates, tracks and maintains study specific trial management tools/systems, and status reports.
Prepares accurate and timely visit reports for all types of visits.
Interacts with internal work groups to evaluate project needs, resources and timelines.
18 months / 2 years independent monitoring experience is essential.
Strong academic life science background.
Ability to travel to Germany once restrictions have eased.
Fluency in German.
If this sounds like the role for you, please apply now
Standard Operating Procedure
Certified Radiology Administrator
Clinical Research Associate