GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Scharf Laboratory in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. The lab located in the Psychiatric and Neurodevelopmental Genetics Unit (PNGU) within the Center of Genomic Medicine and the Departments of Neurology and Psychiatry at MGH investigates genetic and non-genetic risk factors for Tourette syndrome (TS) and related conditions, such as obsessive-compulsive disorder (OCD) and attention deficit hyperactivity disorder (ADHD). In addition to the work we do locally, our group co-leads national and international multi-center genetic and phenotypic studies of TS and related disorders.
We enroll patients with Tourette syndrome and co-occurring neuropsychiatric conditions such as ADHD, OCD, and OC spectrum disorders to participate in our research. In addition to collecting blood or saliva from study participants for future studies of DNA, RNA, and induced pluripotent stem cells, we collect extensive phenotypic information. This includes diagnostic assessments of neurodevelopmental and psychiatric conditions as well as medical, social, and family histories. We utilize online survey-based assessments using REDCap—a secure, web-based application. For those interested in or who have experience with statistics, there are additional opportunities to be involved with data analysis.
We are presently seeking a highly-motivated individual to fill a Clinical Research Coordinator II position beginning in May/June of 2023. The principal duties and responsibilities required of this position are outlined below. This is an excellent opportunity for those interested in pursuing medical school or a PhD in clinical psychology, and affords numerous opportunities for exposure to neurology, psychiatry, and neuropsychiatric genetics. We hope that our research will inform and improve future diagnostic, prognostic, treatment, and prevention strategies for these conditions. The Scharf Lab recognizes that our goals can be accomplished through a team with diverse thoughts, approaches, and backgrounds. Therefore, we encourage candidates from historically underrepresented backgrounds to apply for this opportunity to join our lab.
Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
- 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
- Performs study procedures, which may include phlebotomy.
- Assists with study regulatory submissions
- Writes consent forms
- Verifies subject 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 patient and family
- Monitor and evaluation lab and procedure data
- Evaluate study questionnaires
- Contribute to protocol recommendations
- Assist with preparation of annual review
- May assist PI to prepare complete study reports
Applicants should include a cover letter and resume/CV.
For more information about our research and our group, please visit our websites:
https://scharflab.org (Lab Website)
https://cgm.massgeneral.org/faculty/jeremiah-scharf/ (Center for Genomic Medicine)
- 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
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 acceptability of data results
- Working knowledge of data management program
- Bachelor’s degree required.
- New graduates with some relevant course/project work or those without any prior 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.
SUPERVISORY RESPONSIBILITY (if applicable):
- A Clinical Research Coordinator I does not have any supervisory responsibility.
- A Clinical Research Coordinator II may assist with the training and orientation of new staff members.
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.Apply online here: https://partners.taleo.net/careersection/ghc/jobdetail.ftl?job=3227956&tz=GMT-05%3A00&tzname=America%2FNew_York