CRA II

Proclinical is working with a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. As a CRA, you will have the opportunity to work with innovative therapeutic fields and with challenging studies ranging from phase I - III. We are looking for proactive, positive and self-motivated individuals to join our supportive and dynamic team.

Job Responsibilities:

• Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to the company / Sponsor SOPs and GCP;
• Maintain ongoing site correspondence and site files;
• Complete visit reports and maintaining study-related databases;
• Oversight and interaction with clinical research sites;
• Review of patient charts and clinical research data; and
• Assistance with feasibilities and other tasks upon business requirements.

Skills and Requirements:

• University degree in health-related field;
• 1-4 years previous experience as a CRA;
• Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities;
• Computer literacy;
• Excellent verbal and written communication skills in English and Ukrainian.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Theodora Savlovschi-Wicks on +44 203 7520 314 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.