Job Description
PED-GASTROINTESTINAL DISEASES (IN-PGAS-IUINA)
The Department of Pediatrics employs nearly 1,000 faculty and staff who work alongside employees of Riley Hospital for Children and students of Indiana University School of Medicine (IUSM) to make Riley Children's Health Indiana's largest and most skilled pediatric system. At IUSM, our mission and core values define who we are, how we act, and what we aspire to accomplish.
The Clinical Research Nurse will coordinate two industry studies and participate in drug injections and infusions, teaching families/parents how to administer injections, and evaluation of patient safety and adverse events. This position will complete nursing assessments by the protocol including VS, general physical health and obtaining biospecimens related to IBD and EoE.
General Responsibilities
- Assists the Principal Investigator (PI) and participates in protocol development, evaluation, and review of risk assessment; evaluates study design and risk to subject population; determines staff, facility, and equipment availability; assesses study population/availability.
- Designs recruitment strategies for each assigned study; recruits subjects according to IRB/protocol approved methodologies; consents subjects including discussion of treatment and intervention alternatives; monitors enrollment goals and modifies recruitment strategy as needed.
- Liaisons with health-care professionals/providers to determine best recruitment practices for study; manages subject recruitment including marketing, screening procedures, and enrollment.
- Ensures proper collection, processing, shipment of specimens, and documentation; communicates with laboratory, Principal Investigator, and sponsor regarding laboratory findings; records and documents protocol deviations; communicates with PI and sub-investigators about changes in the trial.
- Participates in preparation and negotiation of study budget and reconciles study budget accounts.
- Reviews, critically evaluates, and comments upon study contracts/agreements.
- Prepares and submits Institutional Review Board (IRB) documents (i.e., Informed Consent, advertisement, protocol and protocol summary).
- Schedules study-related meetings and training sessions and provides instruction to study team for specific study assignments; educates staff regarding scientific aspects of study and trains ancillary staff regarding clinical studies or trials; monitors study team compliance with required study procedures and GCP standards.
- Manages research study inventory and supplies (such as medications, equipment, devices) and maintains required compliance documentation.
- Composes and submits continuing review/amendments/close out information; schedules and prepares for monitor visits; prepares and responds to Sponsor and/or FDA audits.
- Stays up-to-date and maintains current knowledge of regulatory affairs and/or issues; maintains a high level of expertise through familiarity of clinical literature and/or attending continuing education classes, conferences, seminars, and project team meetings.
Combinations of related education and experience may be considered. Education beyond the minimum required may be substituted for work experience. Work experience beyond the minimum required may be substituted for education. Required EDUCATION / WORK EXPERIENCE
- Bachelor's degree in nursing plus 1 year of clinical nursing experience; OR
- Associate's degree in nursing plus 3 years clinical nursing experience; OR
- High school diploma or GED plus LPN plus 4 years of clinical nursing experience
Preferred LICENSES AND CERTIFICATES
Required - LPN Licensed Practical Nurse upon date of hire
Preferred - ACRP or SOCRA Clinical Research Certification upon date of hire
Skills Required - Ability to simultaneously handle multiple priorities
- Experience in a regulated environment
- Demonstrates a high commitment to quality
- Ability to analyze and interpret financial data
- Effective interpersonal skills
- Ability to build strong customer relationships
The role regularly requires the ability to effectively communicate. The role frequently requires the ability to move about the work environment and to position oneself to operate laboratory equipment effectively. The role requires the ability to move objects weighing up to 25 pounds and will occasionally work near moving mechanical parts. The person in this role must be able to perform the essential functions with or without an accommodation.
This position is not eligible for visa sponsorship.
Indianapolis, Indiana
$73,000 - $83,000 annually based on experience, skill level, education, and training.
For full-time staff employees, Indiana University offers a wide array of benefits including:
- Comprehensive medical and dental insurance
- Health savings account with generous IU contributions
- Healthcare and dependent care flexible spending accounts
- Basic group life insurance paid by IU
- Voluntary supplemental life, long-term disability, critical illness, and supplemental accidental death & dismemberment insurance
- Base retirement plan with generous IU contributions, subject to vesting
- Voluntary supplemental retirement plan options
- Tuition subsidy for employees and family members taking IU courses
- 10 paid holidays plus a paid winter break each year
- Generous paid time off plans
- Paid leave for new parents and IU-sponsored volunteer events
- Employee assistance program (EAP)
Learn more about our benefits by reviewing the IU Benefit Programs Brochure.
Career Level: Career
FLSA: Exempt
Job Function: Research
Job Family: Clinical Research
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This posting is scheduled to close at 11:59 pm EST on the advertised Close Date. This posting may be closed at any time at the discretion of the University, but will remain open for a minimum of 5 business days. To guarantee full consideration, please submit your application within 5 business days of the Posted Date.
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Telephone: 812-856-1234
Job Tags
Full time, Work experience placement, Flexible hours,