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Clinical Trials Coordinator
2 months ago
Position Overview
ICON Strategic Solutions is seeking dedicated Clinical Research Coordinators to oversee clinical trials and ensure participant safety.
Key Responsibilities
- Uphold the integrity of clinical trials by adhering to protocols, regulatory standards, and internal guidelines.
- Manage study initiation tasks, including developing recruitment strategies and conducting participant screenings.
- Utilize Clinical Trial Management Systems to maintain accurate records, manage participant reimbursements, and enhance recruitment efforts.
- Maintain ongoing communication with Clinical Operations Management regarding training, recruitment, and trial progress.
- Participate in investigator meetings and contribute to the development of study documentation.
- Collect and document study data accurately, ensuring compliance with protocol requirements.
- Conduct technical procedures as outlined in study protocols, including lab work and participant assessments.
- Continuously evaluate participant eligibility throughout the screening process.
- Document adverse events and communicate findings promptly to investigators and regulatory bodies.
- Foster strong relationships with investigators and provide regular updates on trial status.
- Dispense study medications under the guidance of the investigator.
- Engage with monitors from sponsoring organizations through various communication methods.
- Ensure timely data entry into Electronic Data Capture systems and address queries efficiently.
- Report any protocol deviations to management and assist in maintaining compliance.
- Educate participants about the clinical trial process and facilitate informed consent.
- Support team members as needed based on organizational priorities.
- Prepare for audits by maintaining thorough study documentation and assisting auditors as required.
- Travel to various sites may be necessary to support research activities.