Clinical Research Coordinator

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.