Clinical Research Assistant
Adams Clinical, Bronx, New York, NY +1
What you will do
- Support study start-up activities, including supply inventory, document preparation, and site initiation readiness.
- Assist with participant screening workflows as delegated, including scheduling screening visits and collecting basic information such as demographics, medical history, and other study-relevant details to support eligibility assessment.
- Schedule and prepare for participant visits, including source prep, lab kits, and CRFs.
- Serve as a participant liaison—confirm appointments, coordinate transportation, and maintain ongoing communication.
- Escort and assist participants during on-site visits; perform vital signs, ECGs, and specimen collection/processing as trained.
- Complete accurate, ALCOA+-compliant source documentation for delegated procedures.
- Perform data entry into EDC systems and assist with query resolution.
- Maintain study binders, charts, and logs; support supply management.
- Ensure accurate capture and upload of paper source documents into eSource systems in accordance with site processes and regulatory requirements, supporting long-term retention and audit readiness.