The Clinical Research Coordinator for the Eating Disorders Clinical and Research Program is an integral member of an interdisciplinary team which supports both the functioning of an outpatient clinic and the study of patients and healthy volunteers within a clinical investigational setting in the Psychiatry Department. Under general supervision of the program Co-Directors and Principal Investigators, the coordinator will carry out a broad range of clinical research activities and procedures as indicated below.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The coordinator will be responsible for oversight of clinical research duties including but possibly not limited to the following:
Managing data for several studies concurrently, including psychosocial research, treatment trials, and a clinical data repository
Facilitating data usage by study staff by downloading, cleaning, and distributing data, providing instructions and interpretation materials to ensure best practices when analyzing data
Acquiring extensive knowledge of each dataset in order to act as a resource for all data-related questions
Using R and Microsoft Excel software to clean, visualize, and analyze data
Managing and updating regulatory documents for multiple studies
Ensuring completeness and maintenance of regulatory binders
Aiding in submission of regulatory reports to the IRB
Reviewing and documenting all participant procedures with the PI to ensure all protocol requirements are met
Aiding in submission of grants and IRB proposals
Recruiting and screening of potential participants
Maintaining communication with a vast pool of participants
Administering and rating study interviews and questionnaires
Contributing meaningfully to manuscript writing and revisions
Training and mentoring new and junior coordinators
Performing clinic administrative duties such as scheduling, documenting patient encounters, maintaining clinic documents and materials, and liaising between patients and providers.
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
The Clinical Research Coordinator should also possess:
Careful attention to details
Good organizational skills
Ability to follow directions
Good communication skills
Computer literacy
Working knowledge of clinical research protocols
Ability to demonstrate respect and professionalism for subjects' rights and individual needs
Ability to work independently and as a team player
Analytical skills and ability to resolve technical problems
Ability to interpret acceptability of data results
Working knowledge of data management program
Proficiency in R is strongly preferred.
Qualifications
EDUCATION:
Bachelor's degree required.
EXPERIENCE:
Qualified applicants should have at least one year of previous research experience. Experience with data management and analysis is preferred.
SUPERVISORY RESPONSIBILITY:
No supervisory responsibility.
EEO Statement
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.