Clinical Research Coordinator II - Pediatric Solid Tumor

Dana-Farber Cancer Institute; Boston (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator II for its Pediatric Solid Tumor Program. This role involves supporting clinical trials for adolescent and young adult sarcomas, requiring excellent organizational and communication skills. The position offers full-time opportunities for professional growth in a diverse and inclusive environment.

Qualifications

• Bachelor's Degree required.
• 1-3 years of related experience preferred.
• Experience in medical or scientific research preferred.

Responsibilities

• Support the conduct of clinical trials and research projects.
• Interact with study participants and maintain regulatory documents.
• Prepare regulatory reports and manage study samples.

Skills

Organizational skills

Communication skills

Detail-oriented

Time management

Discretion

Confidentiality

Education

Bachelor's Degree

Tools

Microsoft Office

Job description

Clinical Research Coordinator II - Pediatric Solid Tumor

Join to apply for the Clinical Research Coordinator II - Pediatric Solid Tumor role at Dana-Farber Cancer Institute.

Job Overview

The Pediatric Solid Tumor Program and Sarcoma Center at Dana-Farber Cancer Institute are seeking a motivated and experienced Clinical Research Coordinator. The role involves working within the Clinical Translational Research Program (CTIP) and Sarcoma Program on trials specific to adolescent and young adult (AYA) sarcomas. The Pediatric Solid Tumor Program is one of the largest globally, treating children with various solid tumors and providing innovative therapies. The Sarcoma Center is also a leading group worldwide.

Responsibilities

• Support the conduct of clinical trials and research projects focused on biomarkers and treatments for solid tumors affecting adolescents and young adults.
• Interact with study participants in person and via phone, conduct medical record reviews, develop study intervention materials, maintain regulatory documents, and track study communications.
• Collaborate with research team members including Research Assistants, CRCs, Project Managers, clinicians, and researchers, adhering to Good Clinical Practice guidelines.
• Assist with data reporting, management, source document collection, adverse event reporting, and study record archiving.
• Prepare regulatory reports and IRB submissions, organize study regulatory binders, and ensure data accuracy.
• Manage collection, preparation, and shipment of study samples according to protocol and regulations.
• Coordinate and prepare for audits and study monitoring visits.
• Communicate with sponsors, external sites, labs, and regulatory authorities for specimen-based studies.
• Support the close-out of studies, contribute to research publications, and facilitate communication with regulatory agencies.
• Interact with study participants as required, and assist in chart review and tissue sample work.
• Train new staff members as needed.

Qualifications

• Bachelor's Degree required; 1-3 years of related experience preferred.
• Experience in medical or scientific research or a technology-oriented environment preferred.
• Excellent organizational and communication skills, detail-oriented, and able to manage time effectively.
• Discretion, confidentiality, and proficiency with Microsoft Office are essential.

Additional Information

Dana-Farber is committed to diversity and inclusion, offering an inclusive environment for all staff and patients. The position is full-time, entry-level, and based in Boston, MA. It offers opportunities for professional growth and advancement within the institute.