PRU is looking for
1- 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).
2- nurse with the following qualifications:
1. B.Sc. or diploma in Nursing
2. 1 to 2 years of experience
3. Excellent organizational skills.
4. Accurate, cooperative and committed.
5. Good command of the Arabic and English languages.
If you feel you are qualified for the position please submit your resume to: