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: info@pru.com.jo
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