(Senior) Clinical Research Associate / Lithuania ref number: 37717BR

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;
• Assisting with training, mentoring, and development of new employees, e.g. co-monitoring.

Required education: • University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology); • Fluency in local and English language Required skills, experience: • Minimum 1,5 years of relevant clinical research experience in pharmaceutical or CRO industries • Thorough knowledge of ICH Guidelines and GCP including an understanding of regulatory requirements. • Thorough knowledge of monitoring procedures.

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: 37717BR. Apply now link