SEC Pharma is currently looking for an ambitious Clinical Research Professional to work within a fast paced, busy environment for a leading global contract research company.The successful candidate will identify, select, initiate and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol and in accordance with SOP's/WP's applicable regulations and the principles of ICH-GCP. Provide a benchmark of monitoring competence to inexperienced/less experienced colleagues. Overview of the Role:Independent and proactive coordination of all the necessary activities required to set up, monitor and close out of clinical studies.Travel - domestic and/or international.Expert knowledge of SOP's/WP's, ICH, GCP and appropriate regulations.Maintain timelines. Ensure accuracy and completeness of data entered into systems.Recruitment of investigators.Coaching and mentoring junior colleaguesRole Requirements / Skills / Experience Required:•Bachelor's degree or equivalent in medicine, science or related discipline.•Experience should include monitoring skills. Experience should be a minimum of 1 year of active independent field monitoring and site management experience.•Ability to review and evaluate clinical data.•Computer literacy desirable•Good oral and written communication skills.•A valid Driver's license.For immediate consideration and a full job description please send through your full CV to or call + 44 (0) .