Location: Poland - Homebased
I am currently working on several home-based CRA II positions. In this role you will be working for a global leading CRO at Pharmaceutical companies working on innovative studies on a range of therapeutic areas and phases. If you are an experienced Clinical Research Associate looking for your next exciting opportunity please get in touch to discuss.
Depending on your level of experience, typical duties and responsibilities will include:
Site management visits, including site· evaluation, initiation, routine monitoring and close-out visits
Ensuring the integrity of clinical data through maintenance of site tracking record
Building relationships with investigator site staff to ensure that key clinical metrics are met
Taking part in the development of assigned protocols and Case Report Forms
Assisting in on site co-monitoring visits with more junior members of staff, as required
In order to be considered for CRA positions, you will have:
Independent monitoring experience in a pharmaceutical company or CRO environment. Minimum 1 year
A life science degree or equivalent
Good knowledge of ICH-GCP guidelines and local and international regulatory requirements
Strong verbal and written communication skills
The ability to work independently and in a team
This is one of several positions in the field of Clinical Research that I am currently recruiting for, so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be. Please contact Grace Ticehurst on +441293 584 300 or click Apply Now to submit your CV.
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