Clinical Research Coordinator - Institute for Clinical and Translational Science (ICTS)
Behavioral Health Market Context
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Benefits
Dental CoverageHealth InsurancePaid Time Off
Job Description
pe of study, potential risks and benefits, possible alternatives, and study requirements
• Assist in the design, development, execution, administration, and maintenance of protocols and clinical studies
• Participate in the collection and entry of data into clinical research trial data systems
• Manage and organize regulatory documentation
• Prepare and submit regulatory submissions
• Mentor new students and staff under direction
• Assist with development and administration of budget(s) for study(ies)
• *Qualifications:**
• Bachelor's degree in Nursing (BSN) or an equivalent combination of education and experience
• Minimum of 2 years clinical nursing experience or 1 year of clinical research experience
• Excellent written and verbal communication skills with patients/families, and interdisciplinary team members
• Working knowledge of Good Clinical Practice (GCP)
• Ability to work flexible hours including nights, evenings, and weekends as needed by the research protocol
• A current license to practice nursing in the state of Iowa by the time of hire
• General computer skills
• *Benefits:**
• Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
• Opportunity to work in a dynamic and innovative environment with a team of dedicated professionals
• Professional development and growth opportunities
• Flexible work arrangements, including remote work options within the state of Iowa
• Assist in the design, development, execution, administration, and maintenance of protocols and clinical studies
• Participate in the collection and entry of data into clinical research trial data systems
• Manage and organize regulatory documentation
• Prepare and submit regulatory submissions
• Mentor new students and staff under direction
• Assist with development and administration of budget(s) for study(ies)
• *Qualifications:**
• Bachelor's degree in Nursing (BSN) or an equivalent combination of education and experience
• Minimum of 2 years clinical nursing experience or 1 year of clinical research experience
• Excellent written and verbal communication skills with patients/families, and interdisciplinary team members
• Working knowledge of Good Clinical Practice (GCP)
• Ability to work flexible hours including nights, evenings, and weekends as needed by the research protocol
• A current license to practice nursing in the state of Iowa by the time of hire
• General computer skills
• *Benefits:**
• Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
• Opportunity to work in a dynamic and innovative environment with a team of dedicated professionals
• Professional development and growth opportunities
• Flexible work arrangements, including remote work options within the state of Iowa
Qualifications
- •Bachelor's degree in Nursing (BSN) or an equivalent combination of education and experience
- •Minimum of 2 years clinical nursing experience or 1 year of clinical research experience
- •Excellent written and verbal communication skills with patients/families, and interdisciplinary team members
- •A current license to practice nursing in the state of Iowa by the time of hire
- •General computer skills
Benefits
- •Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
- •Opportunity to work in a dynamic and innovative environment with a team of dedicated professionals
Responsibilities
- •The Clinical Research Coordinator will be an integral member of the research team in the Institute for Clinical and Translational Science (ICTS), providing support for the ICTS mission by performing activities vital to research support endeavors
- •Screen patients for study eligibility and obtain informed consent for clinical trials
- •Educate patients on the scope of study, potential risks and benefits, possible alternatives, and study requirements
- •Assist in the design, development, execution, administration, and maintenance of protocols and clinical studies
- •Participate in the collection and entry of data into clinical research trial data systems
- •Manage and organize regulatory documentation
- •Prepare and submit regulatory submissions
- •Mentor new students and staff under direction
- •Assist with development and administration of budget(s) for study(ies)
- •Working knowledge of Good Clinical Practice (GCP)
- •Ability to work flexible hours including nights, evenings, and weekends as needed by the research protocol
- •Flexible work arrangements, including remote work options within the state of Iowa
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