CLINICAL RESEARCH COORDINATOR (openings in various states as well: MD, VA, GA, IN, TX)
Required:
- 2+ years of experience as a Clinical Research Coordinator
- Experience with oncology protocols preferred
Responsibilities:
- Responsible for the overall successful implementation and ongoing site management of the research studies.
- Actively recruits and screens eligible patients for research protocols as assigned.
- Assists and conducts Informed Consent process.
- Coordinates and implements enrollment and follow-up procedures to collect data from patient charts, medical records, questionnaires, and other sources.
- Performs all study lab processing and shipping as assigned.
- Completes Case Report Forms/Source Templates and pertinent study-related forms accurately and within specified time limits.
- Maintains contact with study patients to facilitate study retention and their care, including communication regarding study requirements, coordinates drug dispensing, and other procedures, treatment, etc.
Benefits:
- Medical, Dental & Vision Plans
- 401k
- Paid Holiday & Vacations
- Employee Assistance Program
- Corporate discounts and much more!
Contact Us:
Please email a copy of your resume and 2-3 professional references to us.