Занятость:
Полная

Опыт работы:
от 2 года(лет)

График работы:
Полный день

Требования:
In order to be successful for this role you need:
• Bachelor's degree in a science related field
• Proven clinical monitoring experience
• At least 1, 5 years clinical trials experience that demonstrates strong attention to details
• Good organizational and time management skills
• Effective interpersonal skills
• Good English language skills
• Proven analytical problem-solving skills
• Ability to work effectively under pressure

Должностные обязанности:
As a clinical research associate your main duties will be:
• perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ich, gcp, fda guidelines, local regulations and ppd sops.
• conduct site visits to assess protocol and regulatory compliance and manage required documentation
• represent ppd and develop and maintain collaborative relationships with investigational sites

Условия работы:
This is not only the opportunity to join a fast growing business, but also the chance to work to a defined career path, providing opportunities for career development.