Assistant Clinical Research Coordinator (entry-level position, 0-1. year experience in Clinical Research preferred)
Duties:
Plan, execute, and assure quality of assigned clinical trials
Perform the Informed Consent Discussion
Complete and/or assist with assigned protocol procedures, chart preparation and recording; completed case report forms; conduct medical histories, and vital signs.
Schedule protocol procedures and visits
Assist in participant recruitment
Assist in data entry
Assist monitors/auditors with data reconciliation
Assist in organizing and maintain lab storage, samples, and specimens
Assist with the collection and packaging of biological samples
Perform clerical and administrative duties as needed
Comply with all study procedures and processes
Requirements
Experience:
Certificate, diploma, or associate’s degree in Medical, Research, or Laboratory Assisting
Two (2) years’ experience as a Medical, Research, or Laboratory Assistant or relevant experience in a laboratory environment
Able to perform vital signs and ECG’s
Able to draw blood (preferred)
Able to multitask, prioritize, and manage time efficiently
Able to work independently or as an active member of a team
Good interpersonal skills and communication
Strong computer skills; Microsoft Office, Excel, etc.
This is an exciting opportunity for individuals interested in contributing to the advancement of medical research and a great opportunity for recent MA and Phlebotomy Graduates.
If you meet the qualifications outlined above and are passionate about clinical research, we encourage you to apply. Please submit your resume along with a cover letter detailing your relevant experience. Only qualified candidates will be contacted for further consideration.