PRU is looking for male Clinical Research Coordinator (CRC), Primary Responsibilities:
. Work directly at patient/subject interface at research sites to deliver high quality patient data in accordance with local regulations, agreed scope of work and as required by protocol.
. Attend and participate in investigator meetings, monitoring visits, audits, seminars and other regional or national meetings.
. Assist with screening and enrolment of subjects into assigned studies.
. Support subjects on trials to encourage maximum retention and future recruitment.
. Assist with the establishment of a recruitment plan for each study.
. Assist investigator with recording and reporting of adverse events and SAE’s as per local regulatory authority guidelines.
. Communicate effectively across all departments company-wide providing information by telephone, in written form, e-mail, or in person.
. Participate in the review of the site-level documentation for assigned clinical studies.
Required Education and skills:
. BSc in clinical sciences, pharmacy or any related Health/Medical.
. Sound knowledge of medical terminology.
. Excellent interpersonal and organizational skills.
. Proficient in the use of Microsoft Office and Excel.
. Fluent in English, spoken and written.
. Ability to establish and maintain effective working relationships with co-workers, managers and clients.
Preferable skills and abilities:
. Sound knowledge of ICH/GCP and Regulatory requirements.
. Certification in Clinical Research is a plus.
. Clinical Research experience in clinical trials (1-3 years).
If you feel you are qualified for the position please submit your resume to the e-mail by clicking on the job application button below the job posting.