Clinical Research Coordinator - Cutaneous

Center for Patient Derived Models - Dana-Farber Cancer Institute; Boston (MA); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading cancer research institute in Boston is seeking a Clinical Research Coordinator to support clinical trials in the Cutaneous program. The role involves managing patient data, ensuring compliance with regulations, and facilitating communication with sponsors. Candidates should possess strong organizational and communication skills, a Bachelor’s Degree, and ideally some experience in research. Join a diverse team committed to advancing cancer treatment and care.

Qualifications

• 0-1 years of related experience preferred.
• Experience in medical or scientific research or a technology-oriented environment preferred.

Responsibilities

• Oversee clinical trial start-up process including protocol review and IRB submissions.
• Manage data reporting, collection of source documents, and study records.
• Ensure proper collection and shipment of study samples.

Skills

Organizational Skills

Communication Skills

Interpersonal Skills

Detail-oriented

Time Management

Education

Bachelor's Degree

Tools

Microsoft Office

Job description

Clinical Research Coordinator - Cutaneous

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Job Ref: 44499
Location: 450 Brookline Ave, Boston, MA 02215
Category: Clinical Research
Employment Type: Full time
Work Location: Onsite: 4-5 days onsite/week

Overview

The Clinical Research Coordinator (CRC) will work within the Cutaneous clinical research program, supporting the research team in conducting clinical trials according to Good Clinical Practice standards under the supervision of the Principal Investigator. Responsibilities include primary data collection and management of patient clinical information related to clinical trials, timely collection and shipment of protocol samples, maintaining regulatory binders, and ensuring compliance with all state, federal, and IRB requirements. The CRC may also handle IRB protocol submissions (amendments, continuing reviews, minimal risk protocols), screen patients for eligibility, obtain informed consents, and register study participants with the Quality Assurance Office for Clinical Trials (QACT). Some travel may be required.

Located in Boston, Dana-Farber Cancer Institute is a leader in cancer research and patient care, committed to diversity, equity, and inclusion, and working with Harvard Medical School-affiliated hospitals to advance treatment and education.

Responsibilities

• Oversee the clinical trial start-up process, including protocol review, IRB submissions, and site activation.
• Manage data reporting, collection of source documents, case report forms, adverse events, and study records.
• Prepare regulatory reports and IRB submissions; organize study regulatory binders and enter study data.
• Ensure proper collection, preparation, and shipment of study samples according to protocol and regulations.
• Coordinate and prepare for audits and monitoring visits.
• Manage communication with sponsors and regulatory authorities.
• Participate in trial close-out activities, including research publications and regulatory communications.
• Interact with study participants as required by the protocol.
• May handle tissue sample work.

Qualifications

• Bachelor's Degree required; 0-1 years of related experience preferred.
• Experience in medical or scientific research or a technology-oriented environment preferred.

Knowledge, Skills, and Abilities

• Excellent organizational and communication skills.
• Strong interpersonal skills for effective interaction at all levels.
• Detail-oriented with the ability to follow through.
• Effective time management and prioritization skills.
• Discretion and adherence to confidentiality guidelines.
• Proficiency in Microsoft Office applications.

At Dana-Farber, we foster an inclusive environment dedicated to reducing the burden of cancer and promoting diversity among our staff. We encourage dedicated, diverse professionals to apply.