Oncology Clinical Research Coordinator - Lewiston, ME (On-Site)

Central Maine Healthcare • Lewiston, ME

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About The Position

Central Maine Healthcare is seeking a Full Time, Clinical Research Coordinator to join our Oncology Team! This position is on-site in Lewiston, Maine. Central Maine Healthcare is an integrated healthcare delivery system serving 400,000 people living in central, western and Midcoast Maine. CMH's hospital facilities include Central Maine Medical Center in Lewiston, Bridgton Hospital and Rumford Hospital. CMH also supports Central Maine Medical Group, a primary and specialty care practice organization. Other system services include the Central Maine Heart and Vascular Institute, a regional trauma program, LifeFlight of Maine's southern Maine base, the Central Maine Comprehensive Cancer Center and other high-quality clinical services. If you are passionate about making a difference and are looking for your next great career opportunity, we look forward to reviewing your application!

Requirements

• Associates degree or a certification in an appropriate allied professional field
• Certification in a medical discipline such as RN, LPN, CNA, PA, etc. required
• 1 year of previous clinical research experience
• Certification as a clinical research coordinator must be achieved within two (2) years of employment

Responsibilities

• Conduct and facilitate the daily activities of a clinical trial
• Assure the safety and welfare of the research trial subjects
• Filing and office organization
• Patient/research participant scheduling
• Patient/research participant history
• Data collection
• Data entry
• Data management
• Follow-up care
• Laboratory procedures
• Order materials/supplies
• Schedule research meetings
• Comply with Institutional policies, SOPs and guidelines
• Adhere to an IRB approved protocol
• Participate in the informed consent process of study subjects
• Support the safety of clinical research patients/research participants
• Coordinate protocol related research procedures, study visits, and follow-up care
• Screen, recruit and enroll patients/research participants
• Maintain study source documents
• Report adverse events
• Understand good clinical practice (GCP) and regulatory compliance
• Educate subjects and family on protocol, study intervention, study drug, etc.
• Manage essential regulatory documents as appropriate
• Complete case report forms (paper & electronic data capture) and address queries
• Submit documents to regulatory authorities (e.g. IRB, FDA, etc.) as directed
• Collect, process and ship laboratory specimens

What This Job Offers

• Job Type: Full-time
• Education Level: Associate degree