Clinical Research Coordinator

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

Requirements

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