Clinical Research Coordinator I, Center for Genomic Medicine
Boston, Massachusetts
Employer: Massachusetts General Hospital(MGH)
Industry: Clinical
Salary: Competitive
Job type: Full-Time
GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Smoller Lab in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. The CRC will work independently for Principal Investigators (PIs) to coordinate, implement, and manage the conduct of clinical and non-clinical research studies of neuropsychiatric diseases. The CRC will work with PIs, study staff, and collaborators to ensure continued progress of studies and team growth through their own contribution of talent, skills, and motivation.
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:
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
Qualifications
EDUCATION:
Bachelor's degree required (preferred in a life sciences field).
EXPERIENCE:
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.
SUPERVISORY RESPONSIBILITY (if applicable):
A Clinical Research Coordinator I does not have any supervisory responsibility.
EEO Statement
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.
The Smoller Lab in the Center for Genomic Medicine at Massachusetts General Hospital (MGH) is seeking a motivated, enthusiastic candidate to join our research group. The CRC will work independently for Principal Investigators (PIs) to coordinate, implement, and manage the conduct of clinical and non-clinical research studies of neuropsychiatric diseases. The CRC will work with PIs, study staff, and collaborators to ensure continued progress of studies and team growth through their own contribution of talent, skills, and motivation.
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
- May assist with drafting content for digital psychological interventions under supervision
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
- Careful attention to details
- Good organizational skills
- Ability to follow directions
- Good communication skills
- Good writing skills
- Computer literacy
- Working knowledge of clinical research protocols
- Ability to demonstrate respect and professionalism for subjects' rights and individual needs
Qualifications
EDUCATION:
Bachelor's degree required (preferred in a life sciences field).
EXPERIENCE:
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.
SUPERVISORY RESPONSIBILITY (if applicable):
A Clinical Research Coordinator I does not have any supervisory responsibility.
EEO Statement
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.
Created: 2024-08-22
Reference: 3301806
Country: United States
State: Massachusetts
City: Boston
ZIP: 02120
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