Clinical Research Coordinator / Orthopaedic Trauma Division

Mass General Brigham•Boston, MA

5d•$20 - $29•Onsite

About The Position

The Brigham and Women's Hospital, Inc. Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Job Summary The Harvard Orthopedic Trauma Initiative is one of the most successful fully integrated cross-campus clinical programs. The Initiative has a very robust clinical research patient-reported outcomes programs that have grown substantially during the last eight years. The CRC I position offers exposure to the clinical research operative, and academic aspects of Orthopedic Trauma Surgery. This on-site position offers terrific opportunities to both work with expert Orthopedic Trauma surgeons and contribute to cutting-edge innovations. Please include a cover letter with your application. Qualifications Working under supervision from the Senior Research Project Manager and/or Principal Investigator, the CRC I will provide support to clinical research studies and outcomes data collection. They may be responsible for the following activities: gathering data from the clinical record; recruiting and enrolling subjects into clinical protocols; developing and implementing patient recruitment strategies and recommending changes to protocols.

Requirements

Bachelor's Degree Related Field of Study required
Some relevant research project work 0-1 year preferred
Work experience in a research setting preferred.
A two year commitment is strongly encouraged.
Sound independent judgement and competence in research methodologies.
Careful attention to detail and good organizational skills.
Ability to follow directions.
Good interpersonal and communication skills.
Computer literacy.
Working knowledge of clinical research protocols.
Ability to demonstrate respect and professionalism for subjects' rights and individual needs.

Responsibilities

Coordinates the implementation - both internally and externally - of sponsored clinical research studies.
Initiates and maintains contact with study participants. Responsible for screening applicants, ensuring they meet appropriate criteria, and makes independent judgment as to the suitability of their participation.
Working in concert with Principal Investigator and/or Senior Research Project Manager or designee, develops and implements subject recruitment strategies.
Reviews and collects appropriate data from the patient clinical record.
Develops, organizes, and/or maintains the study database which is stored at all times on a MGB or BWH network. Responsible for data validation and quality control.
Interacts with subjects with regard to enrollment - including patient education, procedural instruction, and follow-up. May serve as a liaison between subject and physician.
Administers, scores, and evaluates responses to study questionnaires.
In conjunction with Senior Research Project Manager/Principal Investigator, develops and implements new research protocols including design, data collection systems and institutional review board approval.
Performs literature searches as appropriate.
Assists PI or Senior Research Project Manager with preparation for presentation and written published articles.
Assists with regulatory documentation as directed by Senior Project Manager.
All other duties as assigned.