Clinical Research Coordinator II - Attleboro

Satellite Clinical Research CoordinatorThis 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). 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 the 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. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.Demonstrates understanding of CRF completion, including timely and accurate transcription of study dataShows an understanding in coordinating and managing clinical research studiesShows an understanding of ICH/GCP and Federal Regulatory requirementsShows an understanding of DF/HCC SOPsShows 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 trialsAbility to work across satellite locations and provide on-site and remote supportIs competent and autonomous with minimal assistance and supervisionExcellent organization and communications skillsStrong interpersonal skills with the ability to effectively interact with all levels of staff and externals contactsMust be detail oriented and have the ability to follow-throughAbility to effectively manage time and prioritize workloadMust practice discretion and adhere to hospital confidentiality guidelines at all timesMust have computer skills including the use of Microsoft OfficeThe 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.Orients and assists in training new staff.Minimal patient contact.At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.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.