DAY-TO-DAY RESPONSIBILITIES:
- Coordinating clinical trials and managing patient visits for 5 to 7 complex oncology/urology studies.
- Performing clinical tasks and procedures, including phlebotomy, catheter insertion, and handling male and female genitalia.
- Managing study logistics, including scheduling patient imaging, biopsies, and outside vendors.
- Assisting physicians with patient flow and protocol requirements during visits.
- Working alongside central teams to support data entry and patient recruitment tasks.
REQUIRED SKILLS AND QUALIFICATIONS:
- Minimum 3+ years of Clinical Research Coordinator (CRC) experience.
- Strong clinical/medical skill set, including phlebotomy and general medical procedures.
- Experience managing 5 to 7 complex oncology trials and handling high-logistics workflows (scheduling imaging, biopsies, and vendor coordination).
- Direct experience in Urology, Oncology, or Cardiology is preferred (Urology-specific clinical duties can be trained).
- Full willingness to perform hands-on urologic procedures, including handling male and female genitalia and placing catheters.
- Professional demeanor with an assertive, direct communication style suited for fast-paced, highly demanding physicians.
- Geographical flexibility to work out of site in Fairfax, VA, with required willingness to travel to Alexandria and Manasasses locations sometimes.
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Schedule/Shift
Monday - Friday 8 am - 5 pm (ON-SITE)
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