Description
We are seeking a Clinical Research Coordinator to join our team on a part-time basis for 24 hours a week over a period of 6 months.
As a Clinical Research Coordinator, you will be a pivotal member of the site team, involved in various administrative tasks to support investigators and ensure the smooth running of clinical trials. Your responsibilities will include:
- Providing full operational support to investigators, including protocol review, CRF understanding, EDC navigation, and participation in study meetings
- Managing study participants, handling recruitment, screening, informed consent, visit scheduling, study procedures, and ongoing subject communication
- Ensuring regulatory and documentation compliance, preparing ethics submissions, maintaining source documents, entering data, performing QC, and resolving queries
- Executing clinical procedures, such as ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and telemetry monitoring
- Coordinating site operations, including lab logistics, safety reporting, preparation for monitoring visits, audits, inspections, and training of new staff
- Supporting study oversight, contributing to budget/timeline adherence, maintaining training records, and assisting with staffing and scheduling needs
To be successful in this role, you will need:
- A Bachelor's degree in life sciences
- Basic knowledge of clinical trials and experience as a study coordinator
- Availability to work part-time (24 hours per week)
- Availability to work on a fixed-term contract (6 months)
- Experience with recruitment activities is desired