Job type full-time
Not provided by employer
Full job description
Job id: 30351
Location: 450 brookline ave, boston, ma 02215
Category: clinical research
Employment type: full time
Work location: ptl remote: 2-3 days remote/wk
The clinical research coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using good clinical practice under the auspices of the principal investigator(s) and the dfci clinical trials officeThe crc will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trialsEnsures timely collection of protocol related samples including shipment to outside entities as requiredMaintains regulatory binders and ensures study compliance with all state, federal, and irb requirementsMay be responsible for irb protocol submissions (amendments, continuing reviews, and minimal risk protocols)This individual may also screen patients for protocol eligibility, obtain informed consent, and register study participants to clinical trialsSome travel may be required.
Located in boston and the surrounding communities, dana-farber cancer institute is a leader in life changing breakthroughs in cancer research and patient careWe are united in our mission of conquering cancer, hiv/aids and related diseasesWe 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 populationsWe 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.
Oversight of the clinical trials start-up process from receipt of protocols through the scientific review committee and irb submissions, and site activation activities.
Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of data queries.
Prepare and or complete regulatory related reports and irb submissionsMaintain and organize study regulatory binders, enter all required study data on an ongoing basis.
Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and iata/dot regulations.
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits.
Coordination and management of clinical trials, including communication with sponsors and regulatory authorities.
Close-out of clinical trials, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved.
Interact with study participants as directed/required by the protocol and/or study team.
May be responsible for tissue sample work.
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 belongAs relentless as we are in our mission to reduce the burden of cancer for all, we are equally committed to diversifying our faculty and staffCancer knows no boundaries and when it comes to hiring the most dedicated and diverse professionals, neither do weIf working in this kind of organization inspires you, we encourage you to apply.
Bachelor`s degree required, with 0-1 years of related experience preferredExperience working in a medical or scientific research setting or comparable technology orientated business environment preferred.
Excellent organization and communications skills requiredStrong interpersonal skills; 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 office.
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 groups as protected by law.
Posted 2 days ago