Job Details

Clinical Project Managers

Position Number: 9934342
Location: Salt Lake City, United States
Position Type: Laboratory and Research

Clinical Project Managers

Job Summary

Job Summary:
The Division of Hematology, Oncology, BMT has an immediate opening for a Clinical Project Manager in the Department of Pediatrics at the University of Utah Spencer F. Eccles School of Medicine. This position will be responsible to coordinate all aspects of clinical studies from after study initiation for the pediatric oncology team. Participate in site initiation visits. Prepare study-related documentation such as approved informed consent documents, quality of life questionnaires, and laboratory orders, according to the protocol. Maintain required records and ensure compliance with protocols, regulatory regulations, and overall clinical objectives. Record patient registration in management systems, including EPIC, Oncore, RedCap, and iMedidata Rave. Utilize project management methodologies, coordinate with cross-functional teams, resolve issues within the clinical study, and ensure that all targets, timelines, budgets, and requirements are met.
This position may require occasional travel to our Lehi location. Clinical trials are often the standard of care for pediatric, adolescent, and young adult oncology patients, making this role vital not only to division operations but more importantly to the patients and families we serve.
This position is posted at multiple job levels. Each level has distinct qualifications, responsibilities, which will be evaluated during the selection process. Final placement, including the associated pay rate, will be determined based on business needs and budget considerations.

Department Summary:
The Department of Pediatrics is the second largest department in the University of Utah School of Medicine and one of the largest pediatric departments in the country. We are committed to improving the lives of children through excellence in advocacy, education, research, and clinical care. For more information about the Department of Pediatrics, please visit: http://medicine.utah.edu/pediatrics/. Mutual respect and appreciation are highly valued in the department.
Benefits Summary:
The University of Utah offers a comprehensive benefits package including:

Excellent health care coverage at affordable rates (see the Summary Comparison for more information)
14.2% retirement contributions
Generous paid leave time
11 paid Holidays per year
50% tuition reduction for employees, spouses, and dependent children
Flex spending accounts
University provided basic employee life insurance coverage equal to a salary of up to $25,000
Variety of elective insurance coverage, including life insurance, short and long-term disability, accidental death & dismemberment, accident, critical illness, hospital indemnity, and pet.
Free transit on most UTA services
Employee discounts on a variety of products and services, including cell phones & plans, entertainment, health and fitness, restaurants, retail, and travel
Professional development opportunities

Additional benefits information is available at https://benefits.utah.edu/.

Employee Health Requirements:
This position is patient-sensitive and must fulfill all associated vaccination requirements, or be approved for an exemption, prior to the first day of work. We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy. Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.

Responsibilities
Essential Functions:Coordinate all aspects of clinical studies after study initiation for the pediatric oncology team. Prepare study-related documentation such as approved informed consent documents, quality of life questionnaires, and laboratory orders, according to the protocol. Maintain required records and ensure compliance with protocols, regulatory regulations, and overall clinical objectives. Record patient registration in management systems, including EPIC, Oncore, RedCap, and iMedidata Rave. Utilize project management methodologies, coordinate with cross-functional teams, resolve issues within the clinical study, and ensure that all targets, timelines, budgets, and requirements are met.

Coordinate patient recruitment, screening, eligibility verification, informed consent, and enrollment for clinical trials in collaboration with investigators and study teams.
Coordinate protocol-required study visits, procedures, and participant care activities from consent through study completion; prepare and maintain accurate study documentation and records.
Coordinate the collection, processing, and shipment of protocol-required specimens, pathology materials, imaging, and patient-reported outcomes in accordance with study and regulatory requirements.
Identify, document, and report adverse events, serious adverse events, and safety concerns in collaboration with investigators.
Maintain current knowledge of assigned protocols and communicate regularly with investigators, study teams, sponsors, coordinating centers, and consortia regarding enrollment, study progress, protocol updates, and issue resolution.
Ensure the accuracy, completeness, and timeliness of clinical trial data through data entry, validation, reconciliation, query resolution, and maintenance of inspection-ready documentation.
Ensure protocol compliance through quality control activities, documentation review, deviation reporting, regulatory reporting, and support of audits, monitoring visits, and regulatory inspections.
Ensure accurate routing of research-related charges in accordance with institutional and study-specific billing requirements.
Provide cross-coverage and support for team functions as needed and perform other duties as assigned.

The following job levels and associated pay rates will be considered based on job placement. Final placement, including the corresponding pay rate, will be determined by the department in alignment with business needs and budget considerations.Clinical Project Manager, IRequires basic skill set and proficiency. Conduct work assignments as directed. Closely supervised with little latitude for independent judgment.
Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree.This is an Entry-Level position in the General Professional track.

Clinical Project Manager, IIRequires moderate skill set and proficiency in discipline. Conducts work assignments of increasing complexity, under moderate supervision with some latitude for independent judgment.
Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.This is a Developing-Level position in the General Professional track.

Disclaimer:This job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

Minimum Qualifications
EQUIVALENCY STATEMENT: 1 year of higher education can be substituted for 1 year of directly related work experience (Example: bachelor's degree = 4 years of directly related work experience).
Department may hire employee at one of the following job levels:
Clinical Project Manager, I: Requires a bachelor's (or equivalency) with up to 2 years of directly related work experience or a master's (or equivalency) degree. Clinical Project Manager, II: Requires a bachelor's (or equivalency) + 4 years or a master's (or equivalency) + 2 years of directly related work experience.

Preferences
Preferences:

At least 2 years of directly related work experience (or equivalency).
ACRP/SOCRA Certification.

The Department will screen applicants according to the identified preferences.

Special Instructions

Requisition Number: PRN46640B
Full Time or Part Time? Full Time
Work Schedule Summary: Monday -- Friday, between 8:00 a.m. -- 5:00 p.m. Hours may vary based on operational needs. Opportunities for a hybrid two-day weekly telework schedule may be considered after the initial training period, provided the arrangement is supported by operational needs and individual performance. Telework arrangements are not guaranteed and may be modified or discontinued at any time based on business requirements or performance. Employees approved for hybrid telework must provide their own private workspace, secure internet connection, and demonstrate the ability to work independently.
Department: 00857 - Pediatric Hematology/Oncology
Location: Campus
Pay Rate Range: $46,584 - $76,593
Close Date: 01/30/2027
Open Until Filled:

To apply, visit https://utah.peopleadmin.com/postings/211618