Clinical Research Coordinator, Bone Marrow Transplant

Location
Atlanta GA
Salary
Competitive
Posted
Oct 18, 2020
Closes
Nov 17, 2020
Ref
106852
Specialty
Research
Contract Type
Permanent
Hours
Full Time
Position Description
The Clinical Research Coordinator I (CRC I) will support the Bone Marrow Administration department conducting research at Northside Hospital. Responsibilities involve patient registration, data collection, data submission, adverse event reporting, patient follow-up, records management, regulatory reporting, quality assurance and other activities related to research. The CRC I works closely with the Research Team to complete all research required services. Additionally, the CRCI will assist the Research Finance Team to facilitate accurate patient registration and billing.

Research is a major component of the BMT Program at Northside Hospital Cancer Institute. The high quality of our BMT research program has been recognized by the National Institutes of Health, as demonstrated by our designation as a primary core clinical center for the Blood and Marrow Transplant Clinical Trials Network (BMT CTN). Northside Hospital serves as the lead site of a consortium of core clinical BMT centers that includes the University of Miami and Levine Cancer Institute.

Position Requirements
REQUIRED:
1. High school diploma or equivalent with at least Five (5) years of work experience as a Clinical Research Coordinator; OR Graduate of an accredited school of practical nursing, current licensure as a Licensed Practical Nurse in the State of Georgia, at least one (1) year of work experience in a clinical setting, and current American Heart Association’s Basic Life Support Certification (BLS); OR Bachelor's degree (BA or BS) with a preferred degree in allied health, biological sciences, chemistry, or an applicable related field.
2. Experience using spreadsheet, database and word processor applications.
3. Knowledge about clinical research and Good Clinical Practices (GCP). 

PREFERRED:
1. Bachelor’s plus one (1) year or greater of relevant work experience as a Clinical Research Coordinator. 
2. Knowledge of federal grant and clinical trials policy and regulations.
3. Certified Clinical Research Coordinator (CCRC) or working towards certification.

License/Certification Requirements: No

Work Hours: 8:30a-5p

Weekend Requirements: No

On-Call Requirements: No

Similar jobs

More searches like this

Similar jobs