Clinical Research Associate

Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries.

As CRA you will be responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits.

Responsibilities:

- Site administrating and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP;
- Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
- Completing Serious Adverse Event (SAE) reporting, processing production of reports;
- Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned;
- Interact with internal work groups to evaluate needs, resources and timelines.
- Assist with training, mentoring, and development of junior employees, e.g. co-monitoring (for CRAs II and SCRAs);
- Serve as lead monitor for a protocol or project and may assist in establishing monitoring plans as assigned (for CRAs II and SCRAs).

In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.
For more information and to apply online visit www.covancecareers.com, quoting the appropriate reference number.

THERE IS NO BETTER TIME TO JOIN US!
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EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

Regional, CZE

Regional, Czech Republic