Dana-Farber Cancer Institute
Clinical Research Coordinator - Center of Early Detection & Interception Solid T
Dana-Farber Cancer Institute, Boston, Massachusetts, us, 02298
Clinical Research Coordinator - Center of Early Detection & Interception
Building upon Dana-Farber’s deep experience in early cancer detection and treatment, we’ve created a robust, integrated clinical/research program – Centers for Early Detection and Interception. This program brings together Dana-Farber’s expert clinicians and researchers across all cancer types, working together in a unified, multi‑disciplinary effort that will accelerate progress in early cancer detection and interception. Through this effort, we will help stop cancer earlier, saving more lives, and improving the quality of life for all of those affected by cancer.
Responsibilities
Lead patient recruitment and consenting efforts at the Longwood campus, screening for protocol eligibility and obtaining consent from patients for industry‑sponsored and biobanking studies.
Maintain regulatory binders and assure study compliance with all state, federal, and IRB mandates.
Register study participants to clinical trials and operate under guidance of the Principal Investigator(s), the DFCI Clinical Trials Office, and the Clinical Research Director.
Collect, compile, and manage patient clinical information; ensure prompt collection and shipment of protocol‑related samples to external entities as necessary.
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 submissions; maintain and organize study participant/subject trial binder and 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.
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial.
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits.
Coordinate and manage clinical trials throughout the trial life cycle, 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.
Possibility to collect tissue samples per trial requirements.
Data entry of Subject Visit Tracking information, time and effort spent on study‑specific activities, and study‑specific activity into the Clinical Trial Management System contemporaneously.
Bachelor’s Degree or 1 year of Dana‑Farber Associate Clinical Research Coordinator experience required.
0‑1 years of experience working in a medical or scientific research setting or comparable technology‑oriented business environment preferred.
Qualifications
Fluency in English and Spanish, Portuguese, Chinese, or Hatian Creole strongly preferred.
Excellent organization and communication skills.
Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
Detail oriented with the ability to follow‑through.
Excellent time management and prioritization skills.
Discretion and adherence to hospital confidentiality guidelines at all times.
Computer skills including Microsoft Office.
Knowledge, Skills, And Abilities Required
Excellent organization and communications skills required.
Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
Must be detail oriented and have the ability to follow‑through.
Ability to effectively manage time and prioritize workload.
Must practice discretion and adhere to hospital confidentiality guidelines at all times.
Must have computer skills including the use of Microsoft Office.
Patient Contact Contact with adult patients of all ages and populations. Will distribute protocol schedules, quality of life surveys or other study‑related questionnaires, subject diaries, and/or conduct follow‑up communication with patients.
Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications. The hourly range for this position is $23.13/hr - $26.15/hr.
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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Responsibilities
Lead patient recruitment and consenting efforts at the Longwood campus, screening for protocol eligibility and obtaining consent from patients for industry‑sponsored and biobanking studies.
Maintain regulatory binders and assure study compliance with all state, federal, and IRB mandates.
Register study participants to clinical trials and operate under guidance of the Principal Investigator(s), the DFCI Clinical Trials Office, and the Clinical Research Director.
Collect, compile, and manage patient clinical information; ensure prompt collection and shipment of protocol‑related samples to external entities as necessary.
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 submissions; maintain and organize study participant/subject trial binder and 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.
Collaborate with other departments such as Protocol Scheduling, Materials Management, the Clinical Research Laboratory, Pharmacy, Research Nursing, and other departments, as needed per the requirements of the clinical trial.
Responsible for organizing and preparing for both internal and external auditing and study monitoring visits.
Coordinate and manage clinical trials throughout the trial life cycle, 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.
Possibility to collect tissue samples per trial requirements.
Data entry of Subject Visit Tracking information, time and effort spent on study‑specific activities, and study‑specific activity into the Clinical Trial Management System contemporaneously.
Bachelor’s Degree or 1 year of Dana‑Farber Associate Clinical Research Coordinator experience required.
0‑1 years of experience working in a medical or scientific research setting or comparable technology‑oriented business environment preferred.
Qualifications
Fluency in English and Spanish, Portuguese, Chinese, or Hatian Creole strongly preferred.
Excellent organization and communication skills.
Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
Detail oriented with the ability to follow‑through.
Excellent time management and prioritization skills.
Discretion and adherence to hospital confidentiality guidelines at all times.
Computer skills including Microsoft Office.
Knowledge, Skills, And Abilities Required
Excellent organization and communications skills required.
Strong interpersonal skills – ability to effectively interact with all levels of staff and external contacts.
Must be detail oriented and have the ability to follow‑through.
Ability to effectively manage time and prioritize workload.
Must practice discretion and adhere to hospital confidentiality guidelines at all times.
Must have computer skills including the use of Microsoft Office.
Patient Contact Contact with adult patients of all ages and populations. Will distribute protocol schedules, quality of life surveys or other study‑related questionnaires, subject diaries, and/or conduct follow‑up communication with patients.
Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications. The hourly range for this position is $23.13/hr - $26.15/hr.
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