Pracovní náplň
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
Požadujeme
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)
Nabízíme
- 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