Clinical Research Coordinator- Spanish Speaking

3 weeks ago


Boston, United States Massachusetts General Hospital Full time
GENERAL SUMMARY/ OVERVIEW STATEMENT:

The Healthy Aging Studies Lab in the Depression Clinical and Research Program is part of the Outpatient Psychiatry Division of the Massachusetts General Hospital. The Lab is investigating strategies to help people cope with stress, depression, and anxiety, and to make healthy lifestyle changes. The lab employs English and Spanish language mobile health applications and virtual programs to reach a broad range of people. This position will provide invaluable experience for anyone interested in pursuing graduate study in the fields of psychology, public health, or medicine. If you would like to read more about our program, please visit our website at www.depressionmgh.org.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Research Coordinators are responsible for managing and coordinating the clinical studies as members of the research team. This involves patient recruitment, screening patients for study eligibility, scheduling and providing technical support to those who have difficulty using mobile applications, data entry and analysis, manuscript preparation. Research Coordinators will work closely with the physicians and psychologists on staff in managing research participants' care throughout the studies. Additional responsibilities include:

  • Collects & organizes patient data
  • Maintains records and databases
  • Uses software programs to generate graphs and reports
  • Assists with recruiting patients for clinical trials
  • Obtains patient study data from medical records, physicians, etc.
  • Conducts library searches
  • Verifies accuracy of study forms
  • Updates study forms per protocol
  • Documents patient visits and procedures
  • Assists with regulatory binders and QA/QC procedures
  • Assists with interviewing study subjects
  • Administers and scores questionnaires
  • Provides basic explanation of study and in some cases obtains informed consent from subjects
  • Assists with study regulatory submissions
  • Writes consent forms
  • Verifies subject inclusion/exclusion criteria
  • Performs administrative support duties as required


SKILLS/ABILITIES/COMPETENCIES REQUIRED:

  • 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
  • Spanish and English language written and oral fluency


Qualified applicants must have a bachelor's degree, oral and written proficiency in English AND Spanish languages, and strong organizational skills. Psychology, sociology, and premed majors are encouraged to apply, but all are welcome. Prior research or clinical experience is strongly recommended. Experience with databases, Redcap, website management, and basic design are desired but not mandatory.

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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