Clinical Research Coordintor OUD Genomics
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Job Location:
Somerville, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
3 days ago
Vacancies:
1 Vacancy
Job Summary
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.
The Brain Bioethics Lab in the Department of Neurosurgery is seeking a full-time Clinical Research Coordinator (CRC) to join our team. The CRC- will assist with regulatory and operational needs for an NIH-funded study examining the ethical clinical and legal challenges associated with the use of genetic tests for substance use disorders in clinical care. The CRC will work alongside team members to ensure high-quality study execution and compliance. The CRC will contribute to project execution including employing qualitative and survey methods to collect and analyze data and assist with manuscript preparation. This position is ideal for candidates with prior research experience who are looking to work in build upon existing research experience.
Job Summary
SummaryFollowing established policies procedures and study protocols provides assistance on clinical research studies including recruiting evaluating and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy EKGs etc.; and maintaining and updating data generated by the study. Candidates who are in the process of completing their bachelors degree have a six-month grace period from their hire date (up to one year if starting on a per diem basis) to provide degree equivalency verification.
Does this position require Patient Care
No
Essential Functions
-Reviews proposals for compliance with sponsor and organizational guidelines; verifies that all sponsor requirements are met.
-Recruiting patients for clinical trials and conducting phone interviews.
-Verifies the accuracy of study forms and updates them per protocol.
-Prepares data for analysis and data entry.
-Documents patient visits and procedures.
-Assists with regulatory binders and QA/QC Procedures.
-Assists with interviewing study subjects.
-Assists with study regulator submissions.
Qualifications
Education
Bachelors Degree Related Field of Study required
Can this role accept experience in lieu of a degree
Yes
Licenses and Credentials
Experience
Some relevant research project work 0-1 year preferred
Knowledge Skills and Abilities
- 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.
Additional Job Details (if applicable)
Key Responsibilities
Study Coordination and Execution
- Assist with day-to-day study activities including study recruitment coordination and scheduling of study interviews and coordination of team meetings.
- Assist with data collection (semi-structured interviews surveys chart reviews) and quality control checks using REDCap EPIC and other programs.
- Assist with data analysis (qualitative interview data and quantitative survey data) using Dedoose Excel R and other programs.
- Assist with preparation of manuscripts and presentations to disseminate study findings as needed.
Regulatory and Compliance
- Assist with preparation of Institutional Review Board (IRB) protocol submissions amendments and continuing reviews.
Maintain compliance with study protocols Human Subjects and Good Clinical Practice guidelines and institutional policies.
Education & Experience
- Bachelors degree required (genomics health sciences social sciences psychology public health neuroscience or related field preferred)
- 2 years of post-baccalaureate research experience in human subjects research including direct experience with IRB/regulatory documentation.
- Experience with recruiting participants in clinical settings
- Experience with qualitative and quantitative data collection
- Experience analyzing and reporting findings from mixed-methods studies preferred
Skills & Competencies
- Ability to take direction and execute study tasks independently
- Strong organizational time management and problem-solving skills.
- Demonstrate a high degree of flexibility in accepting work assignments with the ability to effectively prioritize tasks understand processes and resolve issues
- Excellent interpersonal and written/verbal communication skills.
- Ability to work independently and collaboratively across multiple investigators and teams.
Remote Type
Work Location
Scheduled Weekly Hours
Employee Type
Work Shift
Pay Range
- /Grade
5EEO Statement:
Mass General Brigham Competency Framework
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.
About Company
Patients at Mass General have access to a vast network of physicians, nearly all of whom are Harvard Medical School faculty and many of whom are leaders within their fields.
