[Hiring] Protocol Coordinator @COG Research Foundation, LLC

Role Description

All staff are employed through the Research Foundation. This role will be in service to COG.

The Protocol Coordinator (PC) serves as the protocol document specialist on the study team for all assigned COG trials. This position is responsible for developing and maintaining clinical research protocols, concepts, site communication memos, study training materials, and other study-related documents under the scientific direction of the Study Chair and COG/Scientific Committee leadership. This includes managing all internal and external review and approval processes throughout the trial, from early study concept to amendments, and coordinating with fellow team members.

The COG Research Foundation, LLC is a 100% remote employer, though some travel may be required. Employee must reside within the United States.

Full salary range for this position: $64,542 to $92,421 per year. The typical hiring range for this position is from $64,542 (minimum) to $78,482 (midpoint), based on 100% FTE. The starting salary is determined based on the candidate’s knowledge, skills, experience, as well as budget availability.

Qualifications

• Experience in clinical research trials and clinical trial protocol development.
• Bachelor’s degree is required, or substitute with four (4) additional years of relevant experience.
• Familiarity with clinical trial components such as statistics, study methodology, informed consent, eligibility, and adverse events.
• 2-3 years of writing experience involving protocols, published manuscripts, grants or other documents related to scientific research is highly desired.
• Clinical research experience in life sciences or related field is desired.
• Demonstrated success and skill at researching, analyzing, and evaluating scientific information.
• Ability to work independently as well as collaboratively with Group staff and investigators.
• High level of computer literacy, including intermediate to advanced knowledge of Microsoft Word.
• Excellent verbal and written communications skills.
• Knowledge of word processing and medical terminology.

Requirements

• Draft informed consent documents and youth information sheets according to COG guidelines.
• Maintain standard COG template language sections in protocol documents.
• Draft study-specific supplemental documents as needed.
• Assist with other projects as needed.
• Perform other duties as assigned.

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.
• Employees who work 20 hours or more per week are eligible for these benefit options.