Brigham and Women's Hospital
Clinical Research Coordinator I
Brigham and Women's Hospital, Boston, Massachusetts, us, 02298
Clinical Research Coordinator I
Brigham and Women’s Hospital
Job Summary:
Under moderate supervision of the Principal Investigator, Senior Research Assistant, or Manager, the Clinical Research Coordinator I supports clinical research studies through recruitment, data collection, scheduling, regulatory submissions, and study monitoring.
Recruit and evaluate patients for research studies, conduct telephone interviews or schedule study visits and screenings.
Collect and organize patient data, maintain and update study databases and the Institutional Review Board (IRB) applications.
Prepare and submit IRB submissions and other regulatory forms in accordance with timelines.
Assist with the development of informed consent documents, source documents, and other study materials.
Communicate with patients/subjects regarding study procedures, education, and follow‑up; serve as liaison between patients and physicians.
Record study visits in the electronic health record (EPIC) while ensuring compliance with institutional policies.
Mail study packets, schedule monitoring visits, and respond to study queries.
Maintain inventory and order supplies as needed, and monitor setup of study equipment.
Support collaborators by providing timely responses to study monitors and contributing to research meetings.
Serve as a back‑up coordinator, cross‑train team members, and assist with other studies as necessary.
Perform any additional duties related to the research team as assigned.
Qualifications:
Ability to follow directions, demonstrate respect for subjects’ rights, possess good interpersonal and communication skills, and maintain careful attention to detail.
Follow research protocols and study instructions accurately.
Meet regulatory timelines and maintain compliance with IRB procedures.
Use computer systems effectively for data entry and reporting.
Communicate effectively with research team members, patients, and clinical care providers.
Demonstrate professionalism and empathy in all interactions.
Assist with creating, filing, and tracking study documents.
Education:
Bachelor’s Degree (BA or BS) required; experience cannot replace the degree.
Experience:
0–1 year of relevant research project work preferred.
Knowledge, Skills and Abilities:
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Respect for subject rights and professional conduct.
Cover Letter Required.
Work Location:
221 Longwood Avenue, Boston, MA.
Schedule:
40 hours per week, Day shift.
Pay Range:
$19.76 – $28.44 per hour.
EEO Statement:
The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation may contact Human Resources at (857)-282-7642.
#J-18808-Ljbffr
Job Summary:
Under moderate supervision of the Principal Investigator, Senior Research Assistant, or Manager, the Clinical Research Coordinator I supports clinical research studies through recruitment, data collection, scheduling, regulatory submissions, and study monitoring.
Recruit and evaluate patients for research studies, conduct telephone interviews or schedule study visits and screenings.
Collect and organize patient data, maintain and update study databases and the Institutional Review Board (IRB) applications.
Prepare and submit IRB submissions and other regulatory forms in accordance with timelines.
Assist with the development of informed consent documents, source documents, and other study materials.
Communicate with patients/subjects regarding study procedures, education, and follow‑up; serve as liaison between patients and physicians.
Record study visits in the electronic health record (EPIC) while ensuring compliance with institutional policies.
Mail study packets, schedule monitoring visits, and respond to study queries.
Maintain inventory and order supplies as needed, and monitor setup of study equipment.
Support collaborators by providing timely responses to study monitors and contributing to research meetings.
Serve as a back‑up coordinator, cross‑train team members, and assist with other studies as necessary.
Perform any additional duties related to the research team as assigned.
Qualifications:
Ability to follow directions, demonstrate respect for subjects’ rights, possess good interpersonal and communication skills, and maintain careful attention to detail.
Follow research protocols and study instructions accurately.
Meet regulatory timelines and maintain compliance with IRB procedures.
Use computer systems effectively for data entry and reporting.
Communicate effectively with research team members, patients, and clinical care providers.
Demonstrate professionalism and empathy in all interactions.
Assist with creating, filing, and tracking study documents.
Education:
Bachelor’s Degree (BA or BS) required; experience cannot replace the degree.
Experience:
0–1 year of relevant research project work preferred.
Knowledge, Skills and Abilities:
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Respect for subject rights and professional conduct.
Cover Letter Required.
Work Location:
221 Longwood Avenue, Boston, MA.
Schedule:
40 hours per week, Day shift.
Pay Range:
$19.76 – $28.44 per hour.
EEO Statement:
The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran’s Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation may contact Human Resources at (857)-282-7642.
#J-18808-Ljbffr