About the role- Manage the participant recruitment process end-to-end, from first contact through prescreening, screening, and consent
- Maintain and report up-to-date recruitment metrics
- Serve as the main point of contact for participants in clinical trials
- Assist with adverse event documentation and reporting
- Assist in writing and updating clinical study documents (CRFs, SOPs, study protocols, ICFs)
- Support IRB and other regulatory submissions
- Develop trial recruitment and other participant-facing materials in accordance with Good Clinical Practice (GCP) guidelines
About you We have preference for at least 2 years of professional experience. Regardless of your career level, you should have:
- Bachelor's degree in a STEM field or similar
- Experience in a patient-facing role in clinical trials
- Experience writing clear and high quality documentation
- Knowledge of basic medical terminology
- Strong organizational and communication skills
- Demonstrated history of exceptional contribution
- High integrity and strong professional judgement
