New 
Clinical Research Coordinator II
 Brigham and Women's Hospital | |
 United States, Massachusetts, Boston | |
| 75 Francis Street (Show on map) | |
 Aug 11, 2025 | |
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General Summary:
You would be a clinical research coordinator at Brigham and Women's Hospital in the Division of Cardiovascular Medicine for 1-2 years. You would work for Dr. Jenifer Brown, who is a cardiologist and principal investigator at BWH, to implement clinical research studies focused on using cardiac imaging and adrenal hormone testing to understand the mechanisms and treatment of primary aldosteronism, hypertension, and heart failure. Our research group focuses on two broad areas: 1) the use of cardiac imaging - including nuclear PET scans and echocardiography (heart ultrasound) - to understand how early changes in the heart's blood flow, structure, and function may lead to clinical heart disease and 2) the prevalence, characteristics, and cardiovascular consequences of adrenal hormone disorders. In this role, you would interact with members of the research team of Dr. Anand Vaidya in the BWH Center for Adrenal disorders and the research team of Dr. Marcelo Di Carli in the BWH Nuclear Medicine/PET division and may participate in the clinical implementation of related clinical research studies. Our research projects include interventional clinical studies, clinical trials, patient registry studies, public health and epidemiology studies, and database related studies. The hallmark characteristic of a productive clinical research assistant in our group is someone who is highly motivated and enthusiastic, well-organized, responsible, and professional. Most clinical research assistants work for 1-2 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. As a research coordinator in Dr. Brown's team, you will work closely with patients in the clinics and closely with human research study participants. You will be responsible for organizing studies, collecting and managing study data, aiding in IRB submission and compliance, and analyzing data on occasion. You will be part of a fun and supportive team of research coordinators, project managers, and physician investigators who will facilitate your professional growth. Job responsibilities include: 1.Coordinates the implementation of clinical research studies. 2.Recruits and evaluates potential study participants. Advertises studies, initiates and maintains subject contact. Schedules subjects. Performs telephone pre-screenings, ensures medical eligibility and makes independent judgment for potential subject suitability. Coordinates research compensation and maintains confidential subject files in a database that includes prescription information, medical correspondence, research data, and follow-up status. 3.May perform clinical tests such as blood pressure measurement, vital signs, and/or venipuncture (venous blood draw) for laboratory testing. 4.Will coordinate visits, specimen collection, and specimen storage. 5.Interacts with study participants, including study participant education, procedural instruction, and follow-up. May serve as a liaison between study participant and physician. 6.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. Maintains study participant research records as part of record keeping function. Responsible for data validation and quality control. 7.Responsible for mailing various study information or packets to study participants. 8.Answers phone calls and inquiries regarding study protocol. 9.Monitors and sets up any needed equipment. Maintains inventory and orders supplies when necessary. 10.In conjunction with Principal Investigator, develops and maintains research protocols and institutional review board approval. 11.Assists with data analysis and manuscript preparation. 12.All other duties, as assigned. Qualifications: BS or BA or equivalent required. Relevant experience in clinical research preferred. Sound independent judgment and competence in research methodologies. Skills/Abilities/Competencies: *Ability to work independently and as a team. *Excellent interpersonal skills for interacting with study participants. *Excellent organizational skills and ability to prioritize a variety of tasks *Careful attention to detail *Ability to demonstrate professionalism and respect for subjects' rights and individual needs. *Good written and oral communication skills *Ability to identify potential problems and trouble-shoot solutions Anticipated start date would be September 2025, but this may be flexible based on candidate availability. Education 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. | |