Clinical Research Coordinator II

Dana-Farber Cancer Institute seeks a Clinical Research Coordinator II to support the conduct of clinical trials under the Principal Investigator and Clinical Research Manager. The role manages trial data, protocol assessments and samples, study documentation and compliance, participant interactions, and coordination throughout the trial life cycle.

Responsibilities

• The CRC (Clinical Research Coordinators) work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator and the Clinical Research Manager
• The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials
• Ensures timely facilitation of trial assessments per protocol and collection of protocol related samples including shipment to outside entities as required
• Will support and maintain participant/subject trial binders and may maintain regulatory binders, to ensure study compliance with all state, federal, and IRB requirements
• May be responsible for pertinent IRB protocol submissions
• This individual may also screen patients for protocol eligibility, obtain informed consent for non-treatment trials, and register study participants with the clinical trials management system, ONCORE
• Some travel may be required
• Oversight of the clinical trials start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities
• Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing, and archiving of study records, and resolution of data queries
• May prepare and or complete regulatory related reports and IRB submissions. Maintain and organize study participant/subject trial binder and regulatory binders, enter all required study data on an ongoing basis and as applicable
• Ensure all study related samples are collected, properly prepared, and shipped according to the protocol requirements and IATA/DOT regulations
• Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial
• Responsible for organizing and preparing for both internal and external auditing and study monitoring visits
• Coordination and management of clinical trials throughout the trial life cycle, including communication with sponsors and regulatory authorities
• Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
• Interact with study participants as directed/required by the protocol and/or study team
• May be responsible for tissue sample collection per trial requirements
• Orients and assists in training new staff
• May have contact with Adult and Pediatric patients of all ages and populations. May distribute protocol schedules, quality of life surveys or other study-related questionnaires, subject diaries, and/or conduct follow-up communication with patients

Preferred

• a background in medical or scientific research or a technology-oriented business environment
• Medical Research Experience
• Scientific Research Experience
• Technology Business Experience

Company

• Cancer treatment and research institute for children and adults
• Boston, Massachusetts, USA
• http://www.dana-farber.org/
• Founded in 1947
• 1001-5000 employees

Qualifications

• Excellent organization and communications skills required
• Strong interpersonal skills – ability to effectively interact with all levels of staff and externals contacts
• Must be detail oriented
• Ability to effectively manage time and prioritize workload
• Must practice discretion and always adhere to hospital confidentiality guidelines
• Must have computer skills including the use of Microsoft Office
• The position requires a bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator
• Candidates should have 1-3 years of relevant experience
• A background in medical or scientific research or a technology-oriented business environment
• The position requires a bachelor's degree or 2 years of experience as a Dana-Farber Clinical Research Coordinator.

Required skills

• Clinical Research

Preferred skills

• $138.08M, 2025-05-06, 2025-11-24, 2026-06-09, 2026-09-04, 2026-10-08, 2026-10-19, 3.9, AI Tools, Benjamin Ebert, Boston Globe, Boston, Massachusetts, USA, Company data provided by, Director, Lurie Family Imaging Center, Elaine and Eduardo Saverin Foundation, Glassdoor, Grant· $1M, Grant· $20M, Grant· $50M, Key Investors, Late Stage, Leadership Team, PR Newswire, Prafulla Gokhale, President and CEO, Recent News, The DeGregorio Family Foundation, Total Funding, Yawkey Foundation, http://www.dana-farber.org

Experience

• 1-3 years