Regional Clinical Project Lead (CPL)
Ray -
Cairo, EgyptPosted 3 years ago65Applicants for3 open positions
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- 0In Consideration
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Job Description
- Provides clinical research expertise in the development and conduct of day-to-day activities through all phases of a clinical trial (start up, recruitment and enrollment, data management, close out and archiving in the middle east UAE, Saudi Arabia, Kuwait ,Qatar, Lebanon, Jordan.
- Assists in planning, managing, implementation and reporting of clinical trials. Oversees preparation and implementation of project specific training programs and training materials for internal staff .
- Evaluate the resources needed vs resources available for the clinical trials running and planned. Provide strategic input aimed at ensuring continuous improvement in the way we operate and implement Standard Clinical Operating Procedures relevant to the purpose of the position. Interact with local Medical, Marketing and other key players to allocate trials (both regional and local as appropriate. Report on status of actual vs planned recruitment from all centers participating in trials in the Country.
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Job Requirements
- Lead, motivate, and set objectives managing performance to assure completion of goals and development of staff. Ensure that prevailing legislation, GCP, Ethical Committee, and standard operating procedures requirements are fulfilled and monitor adherence to and compliance with standard operating procedures.
- Excellent knowledge of Good Clinical Practice (GCP) and International Conference of Harmonization (ICH) guidelines.
- Excellent knowledge of the national and regional regulations for conducting clinical trials.
- Proven ability to work through others to deliver results to the appropriate quality and timeline metrics.
- Proven ability to understand customer needs.
- Effective mentoring and training skills.
- Ability to balance operational and strategic priorities.
- Strong communication and interpersonal skills, including good command of English language, French is a plus.
- Excellent presentation skills.
- Demonstrated proficiency in using systems and technology to achieve work objectives.
- Demonstrated proficiency at analyzing data and information to make conclusions and drive sound decision making.
- Proficient with all computer applications such as Word, Excel, Outlook and PowerPoint.
- More than 6 years of proven experience in the clinical research field and study management.
- A minimum of 2-3 years of experience in a similar managerial position.
- Occasional travel requirements.
- Bachelor degree of medical background (Physician, Pharmacist).
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