Dana-Farber Cancer Institute
Clinical Research Coordinator - GI Oncology
Dana-Farber Cancer Institute, Boston, Massachusetts, us, 02298
Clinical Research Coordinator - GI Oncology
Join to apply for the
Clinical Research Coordinator - GI Oncology
role at
Dana‑Farber Cancer Institute .
The Gastrointestinal (GI) Oncology Clinical Research Program at Dana‑Farber Cancer Institute is seeking a
Clinical Research Coordinator (CRC)
to join the clinical research team. The CRC will be responsible for primary data collection and management of patient clinical information related to participation in clinical trials, ensuring timely collection of protocol‑related samples, maintaining regulatory binders, and ensuring compliance with state, federal and IRB requirements. The CRC may also screen patients for protocol eligibility, obtain informed consent, and register study participants. Some travel may be required.
Responsibilities
Oversee the clinical trials start‑up process from receipt of protocols through Scientific Review Committee, IRB submissions, and site activation activities.
Manage data reporting and collection of source documents, use and development of case report forms, adverse event reporting, and resolution of data queries.
Prepare and complete regulatory reports and IRB submissions, maintain and organize study regulatory binders, and enter required study data on an ongoing basis.
Ensure all study related samples are collected, properly prepared and shipped according to protocol requirements and IATA/DOT regulations.
Organize and prepare for internal and external auditing and study monitoring visits.
Coordinate and manage clinical trials, including communication with sponsors and regulatory authorities.
Conduct trial close‑out activities, including contributing to research articles and audit preparation.
Interact with study participants as directed or required by the protocol and/or study team.
Assist with tissue sample work as needed.
Qualifications
Bachelor's Degree required.
0-1 years of related experience preferred.
Experience working in a medical or scientific research setting or comparable technology‑oriented business environment preferred.
Excellent organization and communication skills.
Strong interpersonal skills and the ability to interact effectively with all levels of staff and external contacts.
Detail‑oriented with strong follow‑through and time‑management abilities.
Adherence to hospital confidentiality guidelines at all times.
Computer skills, including use of Microsoft Office.
Pay Transparency Statement Hourly Range:
$23.13/hr - $26.15/hr
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. We are committed to having faculty and staff who offer multifaceted experiences and to hiring the most dedicated and compassionate professionals.
EEO Statement 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.
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Clinical Research Coordinator - GI Oncology
role at
Dana‑Farber Cancer Institute .
The Gastrointestinal (GI) Oncology Clinical Research Program at Dana‑Farber Cancer Institute is seeking a
Clinical Research Coordinator (CRC)
to join the clinical research team. The CRC will be responsible for primary data collection and management of patient clinical information related to participation in clinical trials, ensuring timely collection of protocol‑related samples, maintaining regulatory binders, and ensuring compliance with state, federal and IRB requirements. The CRC may also screen patients for protocol eligibility, obtain informed consent, and register study participants. Some travel may be required.
Responsibilities
Oversee the clinical trials start‑up process from receipt of protocols through Scientific Review Committee, IRB submissions, and site activation activities.
Manage data reporting and collection of source documents, use and development of case report forms, adverse event reporting, and resolution of data queries.
Prepare and complete regulatory reports and IRB submissions, maintain and organize study regulatory binders, and enter required study data on an ongoing basis.
Ensure all study related samples are collected, properly prepared and shipped according to protocol requirements and IATA/DOT regulations.
Organize and prepare for internal and external auditing and study monitoring visits.
Coordinate and manage clinical trials, including communication with sponsors and regulatory authorities.
Conduct trial close‑out activities, including contributing to research articles and audit preparation.
Interact with study participants as directed or required by the protocol and/or study team.
Assist with tissue sample work as needed.
Qualifications
Bachelor's Degree required.
0-1 years of related experience preferred.
Experience working in a medical or scientific research setting or comparable technology‑oriented business environment preferred.
Excellent organization and communication skills.
Strong interpersonal skills and the ability to interact effectively with all levels of staff and external contacts.
Detail‑oriented with strong follow‑through and time‑management abilities.
Adherence to hospital confidentiality guidelines at all times.
Computer skills, including use of Microsoft Office.
Pay Transparency Statement Hourly Range:
$23.13/hr - $26.15/hr
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. We are committed to having faculty and staff who offer multifaceted experiences and to hiring the most dedicated and compassionate professionals.
EEO Statement 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.
#J-18808-Ljbffr