Posted in Health and Safety
GENERAL SUMMARY/ OVERVIEW STATEMENT
Under the direction of the Principal Investigator, the Clinical Research Coordinator (CRC) is responsible for coordinating and implementing specific aspects of designated research protocols as part of a research team.
The duties of the CRC will include assisting in patient data collection, data-entry, and data organization. The CRC will help to maintain records and databases including working with study physicians to update and maintain an electronic RedCap patient data repository of patients with primary and secondary immune deficiencies. The CRC will help with obtaining patient study data from the medical records and reviewing data for manuscripts. The CRC will also assist with administrative support duties and study regulatory submissions.
Additional responsibilities include:
Collects, compiles, tabulates and analyzes research data. Organizes, establishes and maintains research databases and extracts information. Ensures data is entered accurately and in a timely fashion. Periodically assess quality and completeness of database and subject files. Maintains all required records. Serves as a resource in analyzing and providing statistical information. Assists in chart reviewing for manuscripts, submitting conference abstracts, and publishing manuscripts.
Works closely with principal investigators, research coordinators, and other study staff to identify and screen appropriate candidates for protocols and evaluates criteria for inclusion/exclusion per study protocol. Obtains necessary approvals including written subject informed consent, and demographic information required for subject enrollment.
Collects samples and arranges transport of samples for processing. Collects, analyzes and assures the quality of pertinent subject documentation according to protocol. Maintains confidential subject files, all correspondence, patient information, applicable data and follow-up status of all study subjects. Documents and maintains specific protocol information and communications according to the established guidelines of the unit.
Organizes and participates in project team meetings, prepares the agendas, etc. Establishes effective working relationships with the project team. Contacts subjects and/or families via written and telephone communications for the purpose of explaining the nature of the study and setting up visits and interviews.
- Bachelor's degree required.
- 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.
• Careful attention to detail
• Good organizational skills
• Ability to follow directions
• Good communication skills
• Ability to work independently and as a team player
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.
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