Clinical Research Coordination Lead - Nemours
Jacksonville, FL 32256
About the Job
Essential Functions:
1. Perform routine operational activities for multiple research protocols.
2. Assist with hiring, training, and oversight of research staff.
3. Conducts performance appraisals for direct reports in collaboration with Principal Investigators and Clinical Trials Manager according to Nemours expectations on an annual basis.
4. Develop and sustain a close working relationship with the studies' Principal Investigators (PIs), including regular meetings to discuss projects issues, recruitment, consenting, study execution, specimen processing, specimen shipment, and potential adverse events.
5. Liaise between site research personnel, industry sponsors, PIs, Supervisor, and clinical departments.
6. Collaborate closely with various site departments/teams, including finance, relevant Nemours administrative representatives, and the local IRB, if applicable
7. Coordinate schedule of assessments from initial submission of feasibility until study closeout
8. Provide awareness of research protocols to appropriate site-level personnel, including physicians, nurses, clinical staff, and administrators
9. Document all specific tasks required by the protocol (i.e., medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)
10. Document all patient, staff, and sponsor correspondence, including follow-up encounters, adverse events, interventions, pharmacy dispensations, and patient phone calls.
Qualifications:
- Active SOCRA or ACRP certification, must obtain within one to two years of employment
- Bachelor's Degree required.
- Three to five years clinical research experience.