Position overview
United Research Group is seeking Clinical Research Coordinators at Level I and Level II to coordinate clinical trial activities and support investigators in conducting ethical, compliant, and high-quality clinical research.
Responsibilities and experience expectations will vary according to the assigned coordinator level.
Responsibilities
- Coordinate protocol-required study activities under investigator oversight.
- Support participant identification, screening, enrollment, and retention.
- Facilitate informed-consent processes as appropriately delegated.
- Schedule and coordinate study visits and protocol-required assessments.
- Maintain accurate source documentation and electronic case report forms.
- Assist with adverse event documentation and timely reporting.
- Support investigational product accountability where assigned and appropriately trained.
- Maintain regulatory documents and delegation records.
- Coordinate with monitors, sponsors, CROs, and study personnel.
- Identify and escalate protocol deviations and data quality concerns.
- Support monitoring visits, audits, and regulatory inspections.
The qualifications below are proposed recruitment criteria pending final URG approval.
Proposed qualifications — Clinical Research Coordinator I
- Bachelor's degree in a health-related or scientific field preferred; equivalent relevant experience considered.
- Entry-level to approximately 2 years of clinical research or related healthcare experience preferred.
- Basic knowledge of clinical research regulations and GCP.
- Strong documentation, communication, and organizational skills.
Proposed qualifications — Clinical Research Coordinator II
- Bachelor's degree or equivalent relevant experience preferred.
- Approximately 2–4 years of clinical research coordination experience preferred.
- Demonstrated experience managing clinical trial activities and study documentation.
- Working knowledge of ICH-GCP, informed consent, adverse event reporting, and EDC systems.
- Ability to manage competing study priorities with appropriate investigator oversight.