What are the responsibilities and job description for the Clinical Team Lead position at CEDENT?
Role Summary:
We are seeking a Clinical Team Lead to oversee clinical trial operations, manage a team of research professionals, and ensure the successful execution of study protocols. This role involves site assessments, pre-trial activities, patient recruitment and retention, site monitoring, and study close-out, with a focus on meeting enrollment goals and maintaining compliance with study requirements.
Responsibilities:
- Build and manage a team of Clinical Research Coordinators and Research Assistants.
- Ensure patients are fully informed of the study during the consent process.
- Oversee patient recruitment efforts to meet enrollment targets.
- Create and maintain source documents for study visits.
- Maintain close communication with monitors, sponsors, and investigators.
- Conduct procedures such as vital signs, blood draws, EKGs, and bladder scans, ensuring patients are seen by physicians at required visits.
- Schedule study subjects for necessary visits and procedures, such as pap smears, biopsies, mammograms, and bone scans.
- Collect lab results and procedure reports, ensuring they are reviewed by the investigator.
- Monitor site study supplies to ensure adequacy for trial conduct.
Requirements:
- 4–8 years of experience as a Clinical Research Coordinator, particularly in sponsor-backed trials.
- Strong leadership and team management skills.
Preferred Qualifications:
- Management experience in clinical research settings.
- Bachelor’s degree in a related field.
