Clinical Research Coordinator - Office of Clinical Research

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

Job summary

A leading cancer research institute is seeking a Clinical Research Coordinator to oversee clinical trials and manage data collection. This role involves coordinating with various stakeholders, ensuring compliance with regulations, and contributing to research efforts. The ideal candidate will possess strong organizational and communication skills, along with a Bachelor's degree. Join a mission-driven team dedicated to advancing cancer research and patient care.

Qualifications

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

Responsibilities

• Oversee clinical trials start-up process and manage data reporting.
• Ensure proper collection and shipping of study samples.
• Coordinate and manage clinical trials, including communication with sponsors.

Skills

Organizational Skills

Communication Skills

Interpersonal Skills

Education

Bachelor's Degree

Tools

Microsoft Office

Job description

Job Ref: 44466

Location: 10 Brookline Place West, Brookline, MA 02445

Category: Clinical Research

Employment Type: Full time

Work Location: Onsite: 4-5 days onsite/week

Overview

This Clinical Research Coordinator will be responsible for helping to coordinate a large Dana-Farber Cancer Institute sample and data collection study. The study aims to facilitate the identification, storage, and use of specimens during clinical care, including returning genomic or sequencing results to patients.

Located in Boston and surrounding communities, Dana-Farber Cancer Institute is a leader in cancer research and patient care. Our mission is to conquer cancer, HIV/AIDS, and related diseases. We are committed to creating an inclusive, diverse, and equitable environment, providing compassionate care to patients of all backgrounds, and promoting public health, especially among high-risk and underserved populations. We conduct groundbreaking research, educate future physicians and researchers, and collaborate with partners including Harvard Medical School-affiliated hospitals.

Responsibilities

1. Oversee the clinical trials start-up process from protocol receipt through Scientific Review Committee and IRB submissions, and site activation.
2. Manage data reporting, collection of source documents, development of case report forms, adverse events reporting, and study record archiving.
3. Prepare and complete regulatory reports and IRB submissions. Maintain and organize study regulatory binders. Enter study data regularly.
4. Ensure proper collection, preparation, and shipping of study samples according to protocol and IATA/DOT regulations.
5. Organize and prepare for audits and study monitoring visits.
6. Coordinate and manage clinical trials, including communication with sponsors and regulatory authorities.
7. Handle trial close-out activities, contribute to research articles, and liaise with regulatory agencies.
8. Interact with study participants as required by the protocol and study team.
9. May be responsible for tissue sample work.

Qualifications

We value an innovative, caring, and inclusive environment where everyone feels they belong. We are committed to diversifying our faculty and staff. If you are inspired by this mission, we encourage you to apply.

1. Bachelor's Degree required; 0-1 years of related experience preferred. Experience in medical or scientific research or a technology-oriented business is preferred.
2. Excellent organizational and communication skills are required. Strong interpersonal skills to interact effectively at all levels. Must be detail-oriented, able to follow through, and manage time and workload efficiently. Confidentiality and discretion are essential. Proficiency in Microsoft Office is required.

Dana-Farber Cancer Institute is an equal opportunity employer, affirming the right of every qualified applicant to consideration without discrimination based on race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other protected groups.