Clinical Research Coordinator

3 weeks ago

Boston, United States Mass General Brigham Full time
Clinical Research Coordinator-(3301790)

Description

GENERAL SUMMARY/ OVERVIEW STATEMENT:  

The Department of Pediatrics at Massachusetts General Hospital and the MGH Chelsea HealthCare Center seeks a Clinical Research Coordinator I. Our research team is seeking to educate and engage the Chelsea community on pediatric research while developing a research study defining the cells of nasal passages.Under the general supervision of the Principal Investigators, the CRC I will assist study subjects, staff, and collaborators to manage the day-to-day activities of the sample collection. The CRC I also will work professionally with clinic staff to ensure that clinic protocols are followed. The CRC I will consistently strive to assure and improve the quality of all aspects of the research program. Research activity will primarily be occurring on the MGH Chelsea HealthCare campus but may also occur at the MGH Main Campus.

PRINCIPAL DUTIES AND RESPONSIBILITIES :

Completes required hospital, departmental, disease-specific, and study-specific training. Works directly with subjects to execute assigned studies by: Speaking with patients to assist in recruitment for all related studiesProviding basic explanations of studies to patients and familiesAssists with interviewing study participants to collect accurate study dataAdministering and scoring questionnairesAssist with collecting, processing, and shipping a variety of study related samplesObtain informed consent from subjects for studies, in accordance with hospital policyAttend evening meetings with community groups as part of our community engagement project Assists with study regulatory submissions and maintenance by: Preparing regulatory documents Assisting in budget reviewsAssist with composing and amending consent forms, protocol summaries, and other documents for sponsor and/or IRB reviewAssisting in the completion of Insight e-IRB applicationsEnsuring that study documents are stored, maintained, and routed in compliance with applicable federal, hospital, departmental, and study-specific regulationsMaintaining study records including logs Assists with Quality Assurance/Quality Control and auditing/monitoring procedures by: Self- and peer-reviews documented proceduresWorking to resolve data queries and ensure that data in electronic databases are accurate Works directly with the PIs groups to execute assigned studies by: Assisting with the development and maintenance of RedCap databaseReviewing patient medical records to assist with identifying study candidatesAssists with preparing safety reports and other study progress reports for PIs to reviewEnsuring that PI groups receives results of study tests and proceduresAssist with the development and management of focus groupsSupport the development of a community engagement programin researchRecord meeting notesParticipate and take leadership in community engagement in research projects.

SKILLS/ABILITIES/COMPETENCIES REQUIRED : 

Spanish speaking required, additional languages, including Portuguese, Haitian Creole beneficial Takes initiative when working independently and as an easily-engaged team member. Good verbal & written communication skills and organization skills. Ability to demonstrate respect for and professionalism toward subjects, their rights and individual needs. Careful attention to details Good organizational skills Ability to follow directions Good communication skills Computer literacy, including Office Outlook, Excel, and Word Working knowledge of clinical research protocols is preferred Ability to demonstrate respect and professionalism for subjects’ rights and individual needs

Qualifications

EDUCATION: 

Bachelor’s degree required. 

EXPERIENCE: 

New graduates with some relevant course/project work or those without any prior research experience will be considered for the Clinical Research Coordinator I position outlined above.

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