(Jn TCZ5009) / City of occupation: Praha
CCRI – Czech Clinical Research Institute, a Talentor partner company is searching for suitable candidates for a position of FREELANCE CRA (Clinical Research Associate, Part-time or Full-time, Homebased)
Your future role
This is a home-based role with CZ wide monitoring. Our client works on behalf of a large number of global pharmaceutical companies. As a Clinical Research Associate you will be responsible for performing wing to wing study site management activities. The Clinical Research Associate's Key responsibilities will consist of: - on-site visits and monitoring activities (phase II, III and IV) - Contributes to the site and investigator selection process - providing site-level information for the country recruitment plan - Evaluates site facilities and staff to ensure that it meets ICH-GCP guidelines - assisting and providing feedback on sites issues during site contract development and negotiation process - participating on the investigator meeting and monitors workshop - overseeing and facilitating Start-Up activities - evaluating the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations - raising and closing monitor discrepancies
THE SUCCESSFUL CANDIDATE WILL HAVE - medical / life sciences related field education - minimum 3 years recent monitoring experience is essential - fluent English - ability to work independently with minimal supervision (strong GCP knowledge is a must)
The special thing about this job
- an opportunity for a mid-to-long term cooperation, - multiple opportunities within a broad variety of studies in our portfolio, - competitive hourly rate, - flexible and independent framework based on home-based working framework
If you find this position challenging, please submit your application online. Your consultant, Tomáš Prajzler, email@example.com, will contact you promptly.