PURPOSE: 

The Clinical Research Coordinator (CRC) manages all clinical trial patients enrolled in studies at their assigned GenesisCare, USA office(s). 

Positions available in:

• Clarkston, MI
• Jacksonville, FL
• Plantation, FL
• Myrtle Beach, SC

ESSENTIAL DUTIES AND RESPONSIBILITIES: 

• Coordinates site initiation and study closeout visits
• Tracks patient accrual to protocols
• Attend tumor board meetings 
• Prescreens patients for NCI NCTN, pharmaceutical and investigator-initiated protocols
• In collaboration with physician meets with patients to discuss protocols
• In collaboration with the clinical investigator obtains informed consent from eligible patients
• Works with clinical investigator to confirm patient eligibility
• Registers/randomizes eligible patients to clinical trials 
• Ensures protocol patients receive tests, treatments and evaluations according to the protocol 
• Coordinates monitoring visiting and audits
• Manages all patient and/or protocol data as assigned and responds to queries in a timely fashion
• Completes case report forms per sponsor deadlines
• Maintains regulatory documents
• Submits protocols, amendments, adverse events, etc. to the IRB as necessary
• Other duties as needed

QUALIFICATION REQUIREMENTS: 

• Medical terminology, knowledge of disease processes and anatomy, oncology
• Working knowledge of ICH GCP and regulatory requirements
• Attention to detail and accuracy
• Ability to meet deadlines
• Excellent interpersonal skills
• Excellent written and oral communication skills
• Ability to travel to local / regional offices as needed 

EDUCATION AND/OR EXPERIENCE: 

• Nursing or research background or 
• BS/BA in biology or related field or
• Two years Clinical Trial experience
• Certification with ACRP/SOCRA desired