The position is currently hybrid, requiring 1-2 days per week in the office.

We are seeking a candidate with oncology experience, particularly working with clinical trial protocols.

The Protocol Associate supports the coordination and development of ECOG-ACRIN-sponsored clinical trial protocols, from initial concept through activation, on behalf of the ECOG-ACRIN Medical Research Foundation (EAMRF). This is a non-exempt position.

Responsibilities:

• Oversees assigned disease committees in all aspects of protocol development, which includes, but is not limited to, concept development, protocol development, NCI and CIRB submissions and responses, quality control reviews, tracking development (e.g., OEWG) timelines, and initiating addenda when needed
• Assists with all aspects involved in coordinating protocols for review, editing, and formatting the pro...