Protocol Associate/Translational Science (Oncology Studies) HYBRID

Join a mission-driven organization dedicated to advancing cancer research and improving patient outcomes.

We are seeking a Protocol Associate to serve as the primary laboratory and data coordinator within our Translational Science Team. In this role, you will help manage laboratory projects, biospecimen activities, and research protocols while collaborating with investigators, laboratories, tissue banks, and clinical research professionals across the country.

This is an excellent opportunity for someone with oncology clinical research experience who enjoys coordinating complex projects, working with scientific data, and contributing to groundbreaking translational research.

Location: Hybrid position (Boston office with remote work flexibility)

What You'll Do

• Coordinate laboratory activities for active and proposed translational research studies.
• Support protocol development, data coordination, specimen tracking, and inventory management.
• Maintain and update electronic laboratory databases, including the Sample Tracking System.
• Monitor specimen submissions for clinical trials and retrospective tissue studies, working directly with participating research sites to resolve outstanding submissions.
• Coordinate project related teleconferences and facilitate communication among investigators, laboratories, and other stakeholders.
• Provide informatics support for biospecimen banking and data harmonization initiatives.
• Support the ECOG-ACRIN Navigator concierge by serving as a liaison with tissue banks and biostatisticians to respond to requests from the NCI Navigator and Front Door systems
• Participate in protocol development meetings, disease committee meetings, departmental meetings, and project conference calls
• Review and maintain departmental documentation and Standard Operating Procedures (SOPs).
• Assist with special projects and other responsibilities as assigned.

What We're Looking For

• Bachelor's degree in a life sciences discipline or an equivalent combination of education and relevant experience.
• Minimum of five years of oncology clinical research experience.
• Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
• Excellent written, verbal, and interpersonal communication skills.
• Proficiency with Microsoft Office and electronic data management systems.
• Experience with Good Clinical Practice (GCP) guidelines is preferred.
• Project management experience is a plus.
• Master's degree is preferred.

Why Join Us?

• Competitive salary of $60,000–$72,000, based on experience.
• Hybrid work environment offering flexibility.
• Comprehensive benefits package, including medical, dental, vision, retirement savings, and paid time off.
• Opportunity to work alongside leading oncology researchers and make a meaningful impact on cancer research.
• Collaborative, mission-focused culture dedicated to improving patient care through innovative clinical research.

Equal Opportunity Employer

We are committed to fostering a diverse, equitable, and inclusive workplace where every employee is valued and respected. We are proud to be an Equal Opportunity Employer and consider all qualified applicants without regard to race, color, religion, sex, national origin, age, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by applicable law.