50% Clinical/HC Research Associate - Ryan White Program jobs in United States
cer-icon
Apply on Employer Site
company-logo

University of Iowa · 2 months ago

50% Clinical/HC Research Associate - Ryan White Program

The University of Iowa is seeking a Clinical/HC Research Associate for the Ryan White Program, focusing on delivering and evaluating research protocols for patients living with HIV. This role involves performing clinical activities, developing protocols, recruiting subjects, and ensuring compliance with regulatory guidelines.

EducationHigher EducationUniversities
check
H1B Sponsor Likelynote

Responsibilities

Perform clinical/health care research activities in a skilled/specialized area
Screen patient for study eligibility and consent for clinical trials
Educate patient on scope of study, potential risks and benefits, possible alternatives, and study requirements for patient
Coordinate patient care needs and obtain medical information from local physicians, labs or other providers assuring confidentiality of information according to UIHC policy and HIDAA regulations
Relay information to principle investigator and verify patient eligibility
Administer study medication and identify adverse reactions
Assist in the design, development, execution, administration and maintenance of Virology Clinic protocols and clinical studies and provide input into descriptions of complex research procedures
Assist patients with problems related to protocol. Oversee CRF development
Review query reports. Resolve all monitoring visit issues
Perform and monitor randomizations
Develop complex study materials
Serve as liaison to local health care practitioners, agencies, and sponsors
Screen, recruit, enroll and obtain informed consent for clinical research activities and perform skilled work in a specialized area of research
Oversee the recruitment of subjects and scheduling of trial-related procedures
Prepare study recruitment materials. Develop complex study recruitment materials
Participate in the design; development and testing of clinical research trial data systems
Validate data and make recommendations for resolution
Revise and implement change in data collection
Obtain documentation of the hospitalizations, as well as provide notification to the Principal Investigator, Study Sponsor and FDA as required per protocol
Manage and organize regulatory documentation
Prepare regulatory submissions
Perform on-site audits of research and clinical data
Monitor compliance of regulatory guidelines and proper maintenance of documents
Prepare and present Institutional Review Boards or other submissions and required regulatory documents
May recommend corrective action for reportable events
Maintain records and services provided and work within individual protocol budgets. Assist in writing and submission of initial and continuing reports to the IRB, Radiation Protection Committee, Pharmacy Committee, and other similar research regulatory groups
May provide functional and/or administrative supervision
Mentor new staff under direction
Develop and administer budget for study(ies)
Serve as a liaison to the University Business Office to identify exact patient tests and procedures, which are paid for by study sponsors, and to assist with questions related to billing for protocol treatment procedures

Qualification

Iowa Registered Nurse licenseResearch protocol managementClinical trials experienceHIV/AIDS experiencePatient triage experienceCommunication skillsMentoring skills

Required

A Master's degree in Nursing or an equivalent combination of education and experience is required
A Current, valid Iowa Registered Nurse license is required
Excellent written and verbal communication skills are required
1 year of experience is required
Occasional overnight and weekend travel to study meetings is required

Preferred

Previous experience in HIV/AIDS field or education is desirable
Experience with patient triage is desirable
Research protocol management experience including single and multi-institutional studies and experience with protocol therapy and medical research data management is desirable
Experience with and participation on clinical trials; clinical background and knowledge of regulatory guidelines and procedures is desirable

Company

University of Iowa

company-logo
On our beautiful campus spanning the Iowa River, our faculty and staff enjoy access to an array of cultural, educational, and recreational activities.

H1B Sponsorship

University of Iowa has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (353)
2024 (300)
2023 (244)
2022 (217)
2021 (201)
2020 (193)

Funding

Current Stage
Late Stage
Total Funding
$2.5M
Key Investors
Windgate Foundation
2022-08-17Grant· $2.5M

Leadership Team

leader-logo
Kurt H.
Assoc. Professor, E-MBA Business, UI College of Business; Advised 300 companies globally, CEO
linkedin
leader-logo
Vince Nelson
President & CEO
linkedin
Company data provided by crunchbase