Clinical Research Coordinator, Department of Psychiatry

Site: The General Hospital Corporation

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 Department of Psychiatrys Center for Digital Mental Health (CDMH) at Massachusetts General Hospital is seeking qualified college graduates with a background in psychology neuroscience social work or a related field to fill Clinical Research Coordinator (CRC) positions. CDMH studies evidence-based technology solutions to prevent assess and treat mental illness (e.g. depression anxiety) and to promote mental health.

The CRC will serve as the primary liaison between patients providers and recruiting studies in the center. The CRC will frequently relay clinical and research information and directly resolve patient issues per provider instruction. The patient population is high acuity with complex psychiatric disorders co-morbid medical problems substance use and overlapping psychosocial concerns. The CRC will work as part of a dynamic team of clinicians researchers professional staff and other CRCs to ensure the highest quality of care and service to patients and their clinicians.

The position requires great discretion and judgment to manage sensitive information and effectively prioritize tasks. This challenging and rewarding role would suit a self-motivated individual who enjoys multitasking possesses excellent communication skills and is detail-oriented. The CRC will monitor the pace and progress of recruitment into our research studies and serve as the primary contact for study participants. The CRC will ensure that all components of the participants assessments and surveys are appropriately completed and tracked in the computer database.

To apply please submit your resume/CV and a cover letter. Please list your GPA (cumulative and major) and relevant coursework on your resume/CV.

Principal duties and responsibilities:
- Collects and organizes patient data
- Maintains records and databases
- Uses software programs to generate graphs and reports
- Assists with recruiting patients for studies (e.g. via social media)
- Obtains patient study data from medical records physicians etc.
- Conduct literature searches
- Verifies the 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 participants
- Administers and scores questionnaires
- Provides a basic explanation of the study and in some cases obtains informed consent from participants
- Performs study procedures including electroencephalogram (EEG) skin conductance heart rate and eye-tracking.
- Assists with study regulatory submissions
- Writes consent forms
- Verifies participant inclusion/exclusion criteria
- Performs administrative support duties as required

A Clinical Research Coordinator II performs the duties of a Clinical Research Coordinator I (above) and may also:
- Maintain research data patient fields regulatory binders and study databases
- Perform data analysis and QA/QC data checks
- Organize and interpret data
- Develop and implement recruitment strategies
- Act as a study resource for patients and family
- Monitor and evaluate lab and procedure data
- Evaluate study questionnaires
- Contribute to protocol recommendations
- Assist with the preparation of the annual review
- Assist PI in preparing study reports

Education:

A bachelors degree is required with a background in psychology neuroscience social work or a related field.

Experience:

New graduates with relevant course/project work experience but withoutprior research experience will be considered for the Clinical Research Coordinator I position outlined above.

Those with a minimum of 1-2 years of directly related work experience will be considered for a Clinical Research Coordinator II position.

Knowledge Skills and Abilities:

- Careful attention to details

- Strong organizational skills

- Ability to follow directions

- Excellent written and oral communication skills

- Computer literacy

- Working knowledge of research methods

- Ability to demonstrate respect and professionalism for participants rights and individual needs

- Ability to both work independently (i.e. self-motivated) and as part of a team (i.e. a collaborative team member)

The Clinical Research Coordinator II should also possess:

- Ability to work independently and as a team player

- Analytical skills and ability to resolve technical problems

- Ability to interpret the acceptability of data results

- Working knowledge of data management programs

Hybrid

185 Cambridge Street

40

Regular

Day (United States of America)

Pay Range

$19.76 - $28.44/Hourly

Grade

5

At Mass General Brigham we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive and any offer extended will take into account your skills relevant experience if applicable education certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however it does not encompass all elements contributing to your total compensation addition to competitive base pay we offer comprehensive benefits career advancement opportunities differentials premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

1200 The General Hospital Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religious creed national origin sex age gender identity disability sexual orientation military service genetic information and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment. To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973 the Vietnam Veterans Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990 applicants who require accommodation in the job application process may contact Human Resources at .

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