Clinical Research Coordinator II - Attleboro

Dana-Farber Cancer Institute; Attleboro (MA); On-site; USD 56,000 - 62,700; Full time

Job summary

Dana-Farber Cancer Institute is seeking a Satellite Clinical Research Coordinator in Attleboro, MA to support clinical research and manage patient data related to trials. The role requires a Bachelor's degree and 1 to 3 years of experience in a related field. Responsibilities include managing regulatory documents, ensuring compliance, screening patients, and coordinating research studies. This position offers a salary range of $56,000.00 - $62,700.00 based on experience.

Qualifications

• 1 to 3 years of related experience in a medical, scientific research, or tech environment.
• Ability to manage time and prioritize workload effectively.

Responsibilities

• Support clinical research program and data collection.
• Manage patient clinical information and regulatory documents.
• Ensure study compliance with state, federal, and IRB requirements.
• Screen patients for protocol eligibility and obtain informed consent.
• Travel to Longwood campus and other DFCI sites as required.

Skills

Excellent organization and communication skills

Strong interpersonal skills

Detail oriented

Time management

Discretion and confidentiality

Microsoft Office proficiency

Education

Bachelor's degree

Job description

This Satellite Clinical Research Coordinator position will work within the Dana‑Farber Attleboro Satellite location supporting the clinical research program and research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI disease programs.

The Satellite CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Satellite site(s). He/she ensures timely collection of protocol related samples—including shipment to outside entities as required—maintains site regulatory binders, and ensures study compliance with all state, federal, and IRB requirements. May be responsible for site IRB submissions (violations, deviations, severe adverse event reports). This individual may also screen patients for protocol eligibility, obtain informed consent (minimal risk studies), and register study participants to clinical trials. Travel to the Longwood campus and other DFCI Satellite sites may be required. Position located at Attleboro campus.

Located in Boston and surrounding communities, Dana‑Farber Cancer Institute is a leader in life‑changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high‑risk and underserved populations.

Key Responsibilities

• Demonstrates understanding of CRF completion, including timely and accurate transcription of study data
• Shows an understanding in coordinating and managing clinical research studies
• Shows an understanding of ICH/GCP and Federal Regulatory requirements
• Shows an understanding of DF/HCC SOPs
• Shows an understanding of the roles and responsibilities of other key departments within clinical research (ex. OHRS, ODQ, DFCI CTO etc.)
• Proficient in understanding of phases of clinical trials
• Ability to work across satellite locations and provide on‑site and remote support
• Is competent and autonomous with minimal assistance and supervision

Knowledge, Skills, and Abilities Required

• Excellent organization and communications skills
• Strong interpersonal skills with the ability to effectively interact with all levels of staff and external contacts
• Must be detail oriented and have the ability to follow-through
• Ability to effectively manage time and prioritize workload
• Must practice discretion and adhere to hospital confidentiality guidelines at all times
• Must have computer skills including the use of Microsoft Office

Minimum Job Qualifications

The position requires a bachelor’s degree and 1 to 3 years of related experience. Experience in a medical, scientific research, or technology‑oriented business environment is preferred. The role involves performing primary duties with greater independence and advancing to more complex skill sets as directed.

Supervisory Responsibilities

Orients and assists in training new staff.

Patient Contact

Minimal patient contact.

Equal Opportunity Employment

Dana‑Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.

EEO Poster

Pay Transparency Statement

The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). $56,000.00 - $62,700.00