Clinical Research Coordinator

Nudge • San Francisco, CA

6d

About The Position

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

• 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

Nice To Haves

• At least 2 years of professional experience

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level