Clinical Research Monitoring (CRA)
20–26 an hour
Behavioral Health Market Context
Apply Nowvia Jooble
Job Description
ce with study protocols.
Key Responsibilities:
Prepare visit-specific documentation and charts for the Clinical Research Coordinator
Assist in monitoring subject flow and subject care
Observe, assist, collect, and record data for follow-up visits
Administer required questionnaires to study participants
Request and manage medical records for Serious Adverse Event reporting
Process and ship laboratory biological samples
Obtain written re-consents from study participants when necessary
Complete sponsor-required training and certifications
Perform other duties as assigned
Minimum Qualifications:
Education:
High School diploma or equivalent with relevant experience (Required)
Ophthalmic experience (Preferred)
Experience/Skills:
Previous human subjects research (Required)
Experience with specimen collection/injections
Strong oral and written communication skills
Ability to deliver safe and appropriate patient care in accordance with study protocols
Detail-oriented with excellent organizational skills
Details:
Pay Rate: $20-$26/hr (Dependent on experience)
Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week
Duration: Direct Hire
Seniority level Associate
Employment type Full-time
Job function Research
Industries Research Services
#J-18808-Ljbffr Medix™
Key Responsibilities:
Prepare visit-specific documentation and charts for the Clinical Research Coordinator
Assist in monitoring subject flow and subject care
Observe, assist, collect, and record data for follow-up visits
Administer required questionnaires to study participants
Request and manage medical records for Serious Adverse Event reporting
Process and ship laboratory biological samples
Obtain written re-consents from study participants when necessary
Complete sponsor-required training and certifications
Perform other duties as assigned
Minimum Qualifications:
Education:
High School diploma or equivalent with relevant experience (Required)
Ophthalmic experience (Preferred)
Experience/Skills:
Previous human subjects research (Required)
Experience with specimen collection/injections
Strong oral and written communication skills
Ability to deliver safe and appropriate patient care in accordance with study protocols
Detail-oriented with excellent organizational skills
Details:
Pay Rate: $20-$26/hr (Dependent on experience)
Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week
Duration: Direct Hire
Seniority level Associate
Employment type Full-time
Job function Research
Industries Research Services
#J-18808-Ljbffr Medix™
Qualifications
- •High School diploma or equivalent with relevant experience (Required)
- •Previous human subjects research (Required)
- •Experience with specimen collection/injections
- •Strong oral and written communication skills
- •Ability to deliver safe and appropriate patient care in accordance with study protocols
- •Detail-oriented with excellent organizational skills
Benefits
- •Your actual pay will be based on your skills and experience — talk with your recruiter to learn more
- •Base pay range $20.00/hr - $26.00/hr
- •Pay Rate: $20-$26/hr (Dependent on experience)
- •Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week
Responsibilities
- •We are seeking a Clinical Research Assistant to support our team in conducting high-quality research studies while ensuring patient safety and compliance with study protocols
- •Prepare visit-specific documentation and charts for the Clinical Research Coordinator
- •Assist in monitoring subject flow and subject care
- •Observe, assist, collect, and record data for follow-up visits
- •Administer required questionnaires to study participants
- •Request and manage medical records for Serious Adverse Event reporting
- •Process and ship laboratory biological samples
- •Obtain written re-consents from study participants when necessary
- •Complete sponsor-required training and certifications
- •Perform other duties as assigned
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