Clinical Site Manager
Pharmaceutical Research Unit Amman, Jordan
About the job
Pharmaceutical Research Unit (PRU) or Arab Pharmaceutical Industry Consulting (APIC) is a leading clinical research organization (CRO) that was established in Jordan in 1993. At PRU/APIC we offer clinical development solutions that aim to transform drug development & health industries worldwide. We are the largest CRO in the MENA region – capacity wise- & we pride ourselves on providing a comprehensive list of services to pharmaceutical & healthcare companies at the highest principles of personal & professional conduct.
We have an exciting opportunity for a Clinical Site Manager to support us in our continuous growth.
Summary
The primary purpose of this position is to manage the staff and operations and to enforce quality policy for all clinical site activities and services. The job holder should also provide technical assistance and operational leadership within the clinical site.
Responsibilities:
1. Clinical trial proposal development
2. Manage and coordinate the clinical trials in the department
3. Develop study management plans with the project managers
4. Review the clinical protocols, study reports and related documents
5. Controls and monitors internal and external costs and utilizes available resources
6. Responsible for evaluating performance of clinical research personnel (full time and part time).
7. Plan, identify resources for clinical studies based on project timelines
8. Identify emerging trends/regulations in clinical research while proactively integrating these elements into policies and procedures
9. Development of training programs for internal and external resources
10. Identify quality issues within the study through regular follow ups
11. Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles
Qualifications and experience:
1. Bachelor's degree in life sciences or related fields, with extensive clinical research experience including project management and experience in clinical operations
2. In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements (GCP and ICH guidelines)
3. In depth medical, pharmaceutical and protocol knowledge
4. Strong communication and interpersonal skills, including excellent spoken and written English language
5. Strong organizational and problem solving skills
6. Ability to deliver within the agreed on time-frames
If you feel you are qualified for the position please submit your resume
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