Brigham and Women's Hospital
Clinical Research Coordinator I, Dr. Di Carli Lab
Brigham and Women's Hospital, Boston, Massachusetts, us, 02298
Overview
As a Clinical Research Coordinator I on Dr. Marcelo Di Carli's team, you will work closely with human research study participants. Under the general supervision of the project manager and principal investigators, you will be responsible for organizing research studies, collecting and managing study data, and assisting in data analysis when applicable. You will assist in making judgment regarding the suitability of potential participants for clinical trials, developing and implementing patient recruitment strategies, and adherence to trial protocols.
Our research focus includes understanding cardiovascular physiology and pathophysiology and evaluating the interactions between insulin resistance, inflammation, and vascular disease. Our research projects include interventional clinical studies, clinical trials, patient registry studies, public health and epidemiology studies, and database-related studies. Our group includes the Nuclear Imaging Lab Manager, Nuclear Medicine Research Technologist, 2 clinical research coordinators, 6 research fellows, and multiple principal investigators.
The hallmark characteristic of a productive clinical research coordinator in our group is someone who is highly motivated and enthusiastic, well‑organized, responsible, and professional. Most clinical research coordinators work for 2 years and then matriculate into graduate schools in the health professions (such as medical school, nursing school, MPH, or PhD programs, etc.), however, this is not a requirement or necessary.
Essential Functions
Assist the Nuclear Imaging Lab Manager to coordinate research efforts across the Nuclear Medicine/PET Division and trial sites.
Recruit and evaluate potential study participants. Advertise studies, initiate, and maintain subject contact. Schedule subjects. Perform telephone pre‑screenings, ensure medical eligibility, and make independent judgment for potential subject suitability. Coordinate research compensation, and maintain confidential subject files in a database that includes prescription information, medical correspondence, research data, and follow‑up status.
May perform clinical tests, such as blood pressure measurement, vital signs, and/or venipuncture (venous blood draw) for laboratory testing.
Will coordinate visits and specimen collection, processing, and storage.
Interact with study participants, including study participant education, procedural instruction, and follow‑up. May serve as a liaison between study participant and physician.
Responsible for collecting data and maintaining the study participant information database for studies. May be required to input data, do minimum analysis, and run various reports. Maintain study participant research cords as part of a record‑keeping function. Responsible for data validation and quality control.
Monitor and set up any needed equipment. Maintain inventory and order supplies when necessary.
Submit documentation to the study sponsor as required by trial SOPs. Available during monitoring visits to review source documents and protocols. Respond to sponsor requests for more comprehensive study information, clarifying materials, or addressing queries. Work cooperatively with study sponsor to ensure that good clinical practice and a strict adherence to HIPAA guidelines are being followed.
All other duties, as assigned.
Equal Employment Opportunity The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. 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, to perform essential job functions, and to receive other benefits and privileges of employment.
#J-18808-Ljbffr
Our research focus includes understanding cardiovascular physiology and pathophysiology and evaluating the interactions between insulin resistance, inflammation, and vascular disease. Our research projects include interventional clinical studies, clinical trials, patient registry studies, public health and epidemiology studies, and database-related studies. Our group includes the Nuclear Imaging Lab Manager, Nuclear Medicine Research Technologist, 2 clinical research coordinators, 6 research fellows, and multiple principal investigators.
The hallmark characteristic of a productive clinical research coordinator in our group is someone who is highly motivated and enthusiastic, well‑organized, responsible, and professional. Most clinical research coordinators work for 2 years and then matriculate into graduate schools in the health professions (such as medical school, nursing school, MPH, or PhD programs, etc.), however, this is not a requirement or necessary.
Essential Functions
Assist the Nuclear Imaging Lab Manager to coordinate research efforts across the Nuclear Medicine/PET Division and trial sites.
Recruit and evaluate potential study participants. Advertise studies, initiate, and maintain subject contact. Schedule subjects. Perform telephone pre‑screenings, ensure medical eligibility, and make independent judgment for potential subject suitability. Coordinate research compensation, and maintain confidential subject files in a database that includes prescription information, medical correspondence, research data, and follow‑up status.
May perform clinical tests, such as blood pressure measurement, vital signs, and/or venipuncture (venous blood draw) for laboratory testing.
Will coordinate visits and specimen collection, processing, and storage.
Interact with study participants, including study participant education, procedural instruction, and follow‑up. May serve as a liaison between study participant and physician.
Responsible for collecting data and maintaining the study participant information database for studies. May be required to input data, do minimum analysis, and run various reports. Maintain study participant research cords as part of a record‑keeping function. Responsible for data validation and quality control.
Monitor and set up any needed equipment. Maintain inventory and order supplies when necessary.
Submit documentation to the study sponsor as required by trial SOPs. Available during monitoring visits to review source documents and protocols. Respond to sponsor requests for more comprehensive study information, clarifying materials, or addressing queries. Work cooperatively with study sponsor to ensure that good clinical practice and a strict adherence to HIPAA guidelines are being followed.
All other duties, as assigned.
Equal Employment Opportunity The Brigham and Women's Hospital, Inc. is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. 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, to perform essential job functions, and to receive other benefits and privileges of employment.
#J-18808-Ljbffr