Clinical Research Coordinator
Charlestown, Massachusetts
Employer: Massachusetts General Hospital(MGH)
Industry: Clinical
Salary: Competitive
Job type: Full-Time
GENERAL SUMMARY/ OVERVIEW STATEMENT:
The Massachusetts General Hospital Department of Psychiatry is seeking a full-time clinical research coordinator to assist with the operation of several ongoing research studies as well as future studies. The CRC will work within the Neuroimaging of Mind-Body Interaction and Treatment Laboratory (https://nombit.mgh.harvard.edu/). The objective of the lab is to investigate the interaction between the brain (mind) and body using fMRI, EEG, MEG, and clinical assessments, and translate the findings into clinical practice. The focus of this job will be study management and data collection for several NIH-funded projects investigating neuromodulation and mind-body exercise. This role will include recruiting, scheduling, and performing study visits with adults with chronic pain or cognitive decline as well as healthy individuals. The CRC will be involved with multiple studies.
Please include a resume/CV and cover letter when applying.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
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.
- Collects & organizes patient data
- Maintains records and database
- Assists with recruiting patients for clinical trial
- Verifies accuracy of study form
- Updates study forms per protocol
- Documents patient visits and procedure
- Assists with regulatory binders and QA/QC procedure
- Assists with interviewing study subject
- Administers and scores questionnaire
- 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 submission
- Writes consent form
- Verifies subject inclusion/exclusion criteria
- Performs administrative support duties as required
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
- Careful attention to detail
- Good organizational skill
- Ability to follow direction
- Good communication skill
- Working knowledge of clinical research protocol
- Ability to demonstrate respect and professionalism for subjects' rights and individual need
- Strong interpersonal skills, comfort working with people, and sensitivity towards a neurodiverse population
Qualifications
EDUCATION:
- Bachelor's degree required.
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.
- 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.
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 Massachusetts General Hospital Department of Psychiatry is seeking a full-time clinical research coordinator to assist with the operation of several ongoing research studies as well as future studies. The CRC will work within the Neuroimaging of Mind-Body Interaction and Treatment Laboratory (https://nombit.mgh.harvard.edu/). The objective of the lab is to investigate the interaction between the brain (mind) and body using fMRI, EEG, MEG, and clinical assessments, and translate the findings into clinical practice. The focus of this job will be study management and data collection for several NIH-funded projects investigating neuromodulation and mind-body exercise. This role will include recruiting, scheduling, and performing study visits with adults with chronic pain or cognitive decline as well as healthy individuals. The CRC will be involved with multiple studies.
Please include a resume/CV and cover letter when applying.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
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.
- Collects & organizes patient data
- Maintains records and database
- Assists with recruiting patients for clinical trial
- Verifies accuracy of study form
- Updates study forms per protocol
- Documents patient visits and procedure
- Assists with regulatory binders and QA/QC procedure
- Assists with interviewing study subject
- Administers and scores questionnaire
- 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 submission
- Writes consent form
- Verifies subject inclusion/exclusion criteria
- Performs administrative support duties as required
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
- Careful attention to detail
- Good organizational skill
- Ability to follow direction
- Good communication skill
- Working knowledge of clinical research protocol
- Ability to demonstrate respect and professionalism for subjects' rights and individual need
- Strong interpersonal skills, comfort working with people, and sensitivity towards a neurodiverse population
Qualifications
EDUCATION:
- Bachelor's degree required.
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.
- 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.
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: 2024-09-28
Reference: 3304884
Country: United States
State: Massachusetts
City: Charlestown
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