Clinical Research Coordinator l BWH Allergy

DescriptionThe clinical research assistant will be directly supervised by Dr. Tanya Laidlaw, the Director of the AERD Center, and the Chief of the Section of Translational and Clinical Sciences in the Division of Allergy and Immunology at the Brigham and Women’s Hospital, and in accordance with established hospital policies and procedures. They will help to develop, execute, and oversee work on several research study protocols funded by the NIH and/or pharmaceutical companies, and will maintain the AERD Registry database. They will be responsible for screening, enrolling, and following subjects through the trials, and managing the administrative aspects of these trials. There are many opportunities for patient interaction, including in outpatient clinical settings at study visits, and during sample collection as part of planned surgeries. Additionally, our research assistants often take an active role in writing and publishing the manuscripts that result from their projects, and over a two-year period, most of our clinical coordinators can expect to be a named author on at least 1-2 publications.The Clinical research assistant may also perform literature searches under the direction of supervisor.QualificationsThe principal duties and responsibilities (specific clinical techniques below will be taught, and previous expertise in these areas is not required):Actively responsible for the recruitment of study subjects for AERD Center studies. This includes development and implementation of recruitment strategies, telephone screening of potential subjects, enlisting participation by scheduling appointments and sending out necessary paperwork, and monitoring the studies/ progress to assure data quality and adherence to study-specific protocols as well as timelines.2. Collect biological specimens (blood draws, nasal fluid, urine samples, surgical samples)3. Maintain and organize up-to-date database of all received specimens.4. May draft clinical research forms (CRFs) and build or maintain databases.5. Performing study visits, including the administration of consent, performing PFTs, phlebotomy, following procedures for study visits, and appropriate follow-up with subjects. 6. Collects and reviews study data, ensuring compliance with protocol and data integrity. Drafts corrective action plans for any issues identified through quality control. Ensures queries are responded to in a timely manner.7. Become certified for procedures such as pulmonary function testing (PFT) and phlebotomy (blood draws).8. Medical chart review for demographic and clinical data relevant for patients participating in ongoing studies.Statistical analysis of patient dataQUALIFICATIONS: (MUST be realistic, neither overstated nor understated, and related to the essential functions of the job.)B.S. or B.A.At least one year of work experience in clinical research or internship preferredSKILLS/ ABILITIES/ COMPETENCIES REQUIRED: (MUST be realistic, neither overstated nor understated, and related to the essential functions of the job.)Strong organizational and communication skills.· Excellent interpersonal skills are required for working with the study participants.Experience in a clinical environment.Strong analytical and computer skills required, proficiency with Microsoft Access, Excel, Word, and Outlook. Proficiency in Research Electronic Data Capture (REDCap) preferred.Effective problem-solving skills. WORKING CONDITIONS: Describe the conditions in which the work is performed.Will work in the Brigham and Women’s Hospital Main Campus and associated Mastocytosis Center facilities and shared offices offices. Additional work will be at the BWH Mastocytosis Center at the 850 Boylston Street site in Chestnut Hill, MA. Job Field: ClinicalOrganization: Brigham & Women's Hospital(BWH)Schedule: Full-timeShift: Day JobEmployee Status: Regular