NCORP Project Coordinator

Responsibilities:

• Coordinate and support the preparation, review, and maintenance of documentation related to CCDR research protocols.
• Maintain internal study records and track important study events through COG tracking applications.
• Draft informed consent documents and youth information sheets according to COG guidelines.

Qualifications:

• Minimum three years of related work experience, preferably in a clinical research setting.
• Bachelor’s degree in a science or related field or substitute with four additional years of related experience.
• Excellent oral and written communication skills, including the ability to draft, review, and organize professional documents.

Benefits:

• Comprehensive benefit options include medical, dental, vision, 401(k), accrued Paid Time Off (PTO).
• Employee Assistance Program (EAP), Flexible Spending Account (FSA).
• Cell phone and internet stipends, wellness stipend, paid holidays, and more.