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You will be updated with latest job alerts via emailMass 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
GENERAL SUMMARY/ OVERVIEW STATEMENT:Qualifications
PRINCIPAL DUTIES AND RESPONSIBILITIES:
The following duties will be performed independently:
Verifies consent process and patient eligibility via source documentation review
Ensures completeness of source documentation to confirm eligibility
Works with study teams to resolve any discrepancies relating to subject eligibility
Maintains a log of completed registration to assist with program metrics
Enters subject registration information into the registration system (OnCore)
Collaborate with study team on eligibility checklist revisions
Provides education to study teams on consent and eligibility documentation practices
Provides monitoring to ensure protocol compliance
Specialized projects as assigned by the Program Manager
Contribute to continuous quality assurance initiatives within the program
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
Exceptional time management skills with the capacity to prioritize among multiple tasks
High degree of computer literacy
Ability to work independently and as a team member
Problem-solving skills including the ability to gather information identify resources and develop alternatives
Ability to interpret acceptability of data results and identify incorrect or incongruent data
Working knowledge of clinical trial data management platforms (e.g. Medidata Rave OnCore) for subject registration data review and tracking compliance
Able to work successfully in a remote environment and demonstrate initiative and accountability
Working knowledge of clinical research protocols
Effective written and verbal communication skills including comfort presenting information to study teams
Initiative and accountability in identifying and following through on quality issues or process improvements
Capacity to support training and provide informal guidance to peers
Additional Job Details (if applicable)
LICENSES CERTIFICATIONS and/or REGISTRATIONS:
None
EDUCATION:
Bachelors degree required
EXPERIENCE:
2-4 years of clinical trial or related experience required
SUPERVISORY RESPONSIBILITY:
May assist with orientation training and mentoring of new staff
FISCAL RESPONSIBILITY:
None
WORKING CONDITIONS:
Duties will be performed in a remote setting. Applicants may work in all states with the following exceptions: WY ND Puerto Rico and the U.S. Virgin Islands.
Monday Friday 9:30am 6pm ET
Does not include patient contact
Remote Type
Work Location
Scheduled Weekly Hours
Employee Type
Work Shift
Pay Range
$49504.00 - $72404.80/AnnualGrade
6EEO Statement:
At Mass General Brigham our competency framework defines what effective leadership looks like by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance make hiring decisions identify development needs mobilize employees across our system and establish a strong talent pipeline.
Full-Time