Beth Israel Lahey Health
Clinical Research Coordinator I (Vascular Cell Biology)
Beth Israel Lahey Health, Boston, Massachusetts, us, 02298
Overview
The purpose of the
Clinical Research Coordinator I
is to coordinate clinical research activities for the Joslin 50-year Medalist Study, which was established to study protective factors against diabetic complications in individuals with type 1 diabetes. This individual will, on a daily basis, be involved in recruiting patients, conducting study visits, as well as processing specimens and entering data. Additionally, they will communicate with participants in regards to issues related to the study. The individual will also be trained to conduct cognitive and brain imaging studies including assisting with image processing. The health care organization states a policy to protect patients, colleagues and communities. We require that all staff be vaccinated against influenza (flu) as a condition of employment.
Responsibilities
Aids in the creation and implementation of recruitment strategies and coordinating all aspects of active studies in the Medalist Program.
Identify eligible participants
Inform patients of research and eligibility
Recruiting and scheduling study participants
Assess inclusion/exclusion criteria
Assists with collecting, completing and maintaining study data collection forms and source documents.
Administer questionnaires
Maintain research patient records and regulatory binders
Prepare weekly recruitment reports
Performs routine laboratory and clinical procedures (including measuring blood pressure, height and weight, administering cognitive function tests).
Process and store biological specimens
Maintain organization of biological specimens
The individual will be trained to run brain MRI processing pipelines. They will help check the scans for quality control, and batch process the images through the established pipelines and assist with data analysis using the output data to correlate with clinical data.
Tracks and ships biological samples for assays.
Coordinating post-mortem organ donation study.
Assists in making amendments to protocols and submit proper documentation to IRB.
Performs other duties as needed.
Qualifications
Bachelor’s Degree
0-3 years of relevantexperience, preferably in clinical research, undergraduate experience in scientific research and/or data management also preferred
Excellent written and verbal communication skills
Excellent interpersonal/human relations skills
Highly organized and efficient
Attentiveness to detail
Ability to maintain confidentiality
Ability to operate personal computer and various software packages (Microsoft Office)
Location
US-MA-Boston
Job ID
N3892-25
# Positions
1
Category
Research - Research
Pos. Type
Full Time
All of the employing entities of Beth Israel Lahey Health maintain a continuing policy of non-discrimination in employment. The policy is to provide equal opportunity and access for all persons, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or status as a protected veteran, in all phases of the employment process and in compliance with applicable federal, state, and local laws and regulations.
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The purpose of the
Clinical Research Coordinator I
is to coordinate clinical research activities for the Joslin 50-year Medalist Study, which was established to study protective factors against diabetic complications in individuals with type 1 diabetes. This individual will, on a daily basis, be involved in recruiting patients, conducting study visits, as well as processing specimens and entering data. Additionally, they will communicate with participants in regards to issues related to the study. The individual will also be trained to conduct cognitive and brain imaging studies including assisting with image processing. The health care organization states a policy to protect patients, colleagues and communities. We require that all staff be vaccinated against influenza (flu) as a condition of employment.
Responsibilities
Aids in the creation and implementation of recruitment strategies and coordinating all aspects of active studies in the Medalist Program.
Identify eligible participants
Inform patients of research and eligibility
Recruiting and scheduling study participants
Assess inclusion/exclusion criteria
Assists with collecting, completing and maintaining study data collection forms and source documents.
Administer questionnaires
Maintain research patient records and regulatory binders
Prepare weekly recruitment reports
Performs routine laboratory and clinical procedures (including measuring blood pressure, height and weight, administering cognitive function tests).
Process and store biological specimens
Maintain organization of biological specimens
The individual will be trained to run brain MRI processing pipelines. They will help check the scans for quality control, and batch process the images through the established pipelines and assist with data analysis using the output data to correlate with clinical data.
Tracks and ships biological samples for assays.
Coordinating post-mortem organ donation study.
Assists in making amendments to protocols and submit proper documentation to IRB.
Performs other duties as needed.
Qualifications
Bachelor’s Degree
0-3 years of relevantexperience, preferably in clinical research, undergraduate experience in scientific research and/or data management also preferred
Excellent written and verbal communication skills
Excellent interpersonal/human relations skills
Highly organized and efficient
Attentiveness to detail
Ability to maintain confidentiality
Ability to operate personal computer and various software packages (Microsoft Office)
Location
US-MA-Boston
Job ID
N3892-25
# Positions
1
Category
Research - Research
Pos. Type
Full Time
All of the employing entities of Beth Israel Lahey Health maintain a continuing policy of non-discrimination in employment. The policy is to provide equal opportunity and access for all persons, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or status as a protected veteran, in all phases of the employment process and in compliance with applicable federal, state, and local laws and regulations.
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