JOB TITLE: Clinical Trial Monitor
JOB LOCATION: Abuja
JOB DETAILS:
- Responsible for all activities related to the implementation of the clinical monitoring of study and assure work is done according to the approved protocol.
- Work with TES Technical Coordinator to develop and implement Clinical Monitoring Plan as required by SOP
Team Duties / Responsibilities:
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- Responsible for assuring needs of clinical sites are met by facilitating clinical monitoring processes including:
- Regulatory document collection and review.
- Develop site/monitoring tools and training materials.
- Review and identify trends in enrolment and data entry at sites and proactively interface. with Principal Investigator and clinicians at site to identify solutions.
- Oversee monitoring visit schedule to ensure compliance with frequency.
- Manage quality and regulatory compliance among investigational sites.
- Assist TES Technical Coordinator with the preparation of information for inclusion in monthly report to client.
Knowledge, Skills and Competencies
- MD (or equivalent) with a minimum of at least 5 years’ experience in clinical research and /or as a Clinical Monitor.Thorough knowledge of clinical research process.
- Excellent organizational and interpersonal skills.
- Positive attitude and ability to interact with all levels of staff to coordinate and execute study activities.
- Ability to manage multiple priorities within clinical trials.
- Working knowledge of current ICH GCP guidelines and applicable regulations in Nigeria.
Job Features
Job Category | Engineering / Technical |