Research Program Manager

Job Summary:

The Division of Urology seeks a Research Program Manager to oversee and coordinate a diverse portfolio of basic clinical translational and academic research activities. This position serves as a central resource for investigators faculty staff trainees and collaborators by providing research administration regulatory guidance study and project management support grant and publication tracking compliance oversight and research consultation. The Research Program Manager supports research activities across multiple disciplines and funding sources facilitates onboarding and training for research personnel and promotes operational efficiency regulatory compliance and scholarly productivity. The position independently manages research operations and resource allocation for the Divisions research portfolio and plays a key role in advancing the Divisions overall research and academic mission through strategic coordination process improvement and collaborative leadership.

Key Responsibilities:

Research Operations Coordination & Program Management 35%

• Lead and coordinate the day-to-day operations of the Divisions research portfolio including basic translational clinical and academic research activities.

• Serve as a primary resource and coordinator for research projects and initiatives from concept development and feasibility assessment through project completion and dissemination of results.

• Independently manage research activities in accordance with institutional policies sponsor requirements regulatory guidelines and applicable federal state and university regulations.

• Coordinate research project initiation implementation monitoring reporting and closeout activities across multiple research programs and funding sources.

• Maintain knowledge of research protocols project requirements compliance standards and operational processes to ensure successful execution of research activities. Clinical JA (3) Word

• Support research participant recruitment screening enrollment informed consent retention and follow-up activities as applicable while also supporting non-human-subject research initiatives.

• Ensure research resources equipment databases and operational infrastructure are available and effectively managed to support divisional research activities.

• Collaborate with investigators faculty trainees sponsors institutional research offices and external partners to facilitate successful research and scholarly activities.

• Serve as the primary liaison among investigators research personnel trainees sponsors institutional departments and research collaborators to support the Divisions research mission.

Regulatory Compliance Research Administration & Quality Management 20%

• Ensure compliance with applicable federal regulations institutional policies sponsor requirements IRB requirements FDA regulations ICH-GCP guidelines and other research compliance requirements as applicable. Maintain complete and accurate regulatory documentation study files project records essential documents and other research documentation. Manage Institutional Review Board (IRB) submissions including initial applications continuing reviews amendments reportable events and study closures.

• Develop protocol-specific source documents workflow tools Standard Operating Procedures (SOPs) Case Report Forms (CRFs) process maps training manuals and quality assurance documentation.

• Identify compliance risks proactively prevent protocol deviations implement corrective actions and ensure Principal Investigator oversight requirements are met.

• Lead quality improvement initiatives to enhance regulatory compliance operational consistency and research quality across multiple research programs and projects.

Leadership Supervision & Staff Development 20%

• Provide leadership and daily operational oversight for division research coordinators students research residents and other research personnel across multiple hospital locations.

• Train mentor and onboard new research staff while ensuring ongoing competency in research regulations study procedures and institutional policies. Evaluate staffing needs assign and redistribute workloads prioritize daily operations and provide guidance to ensure efficient study management.

• Conduct annual performance evaluations and provide coaching professional development and performance feedback for research staff. Identify training opportunities and foster continuous learning and professional growth within the research team.

• Serve as the division Subject Matter Expert (SME) for research operations regulatory compliance and best practices.

Data Management Research Support & Scientific Collaboration 15%

• Oversee accurate collection coding validation analysis interpretation and reporting of research data.

• Maintain research databases and research management systems including OnCore REDCap and other electronic data capture systems. Review research proposals and conduct literature reviews to support investigators and research initiatives.

• Assist investigators residents fellows and medical students with research design abstracts manuscripts presentations and publication efforts.

• Monitor and report division research productivity including publications abstracts conference presentations enrollment metrics and study milestones.

• Present research updates study progress operational metrics and findings during team and investigator meetings.

Strategic Planning Financial Management & Process Improvement 10%

• Lead research feasibility assessments and develop strategic plans to support successful project implementation recruitment retention and overall research program growth.

• Design implement and evaluate operational workflows to improve efficiency regulatory compliance research performance and stakeholder experience.

• Develop monitor and manage research project and program budgets ensuring financial feasibility sponsor compliance and appropriate cost recovery.

• Analyze operational performance metrics and provide strategic recommendations to leadership for continuous process improvement.

• Develop contingency plans optimize research workflows and implement innovative solutions to support successful research program execution and long-term program growth.

Work Location:

Onsite this role is expected to work onsite and is located in Aurora Colorado.

Why Join Us:

The Division of Urology is seeking a collaborative and highly organized Research Program Manager to support and advance a diverse portfolio of basic translational clinical and academic research activities. This position will partner with faculty staff trainees and institutional stakeholders to strengthen research operations support regulatory compliance track scholarly productivity and enhance the Divisions overall research mission.

Why work for the University

We haveAMAZINGbenefits and offerexceptional amounts of holiday vacation and sick leave! The University of Colorado offers an excellent benefits package including:

• Medical: Multiple plan options

• Dental: Multiple plan options

• Additional Insurance: Disability Life Vision

• Retirement 401(a) Plan: Employer contributes 10% of your gross pay

• Paid Time Off: Accruals over the year

• Vacation Days: 22/year (maximum accrual 352 hours)

• Sick Days: 15/year (unlimited maximum accrual)

• Holiday Days: 15/year

• Tuition Benefit: Employees have access to this benefit on all CU campuses

• ECO Pass: Reduced rate RTD Bus and light rail service

There are many additional perks & programs with the CU Advantage.

Qualifications:

Minimum Qualifications:

• Bachelors degree in public health public administration social/behavioral sciences physical sciences nursing healthcare finance accounting business administration business or a directly related field from an accredited institution and 4-6 years of professional experience supporting research programs research administration research operations clinical research academic research or a related research environment.

• A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelors degree on a year for year basis.

Applicants must meet minimum qualifications at the time of hire.

Preferred Qualifications:

• Five (5) years of research administration research program management clinical research academic research or related experience in an academic medical center or higher education environment.

• Experience supporting multiple types of research activities including basic translational clinical or outcomes research.

• Supervisory or team leadership experience.

• Exceptional interpersonal and communication skills.

Conditions of Employment:

• Applicants must be legally authorized to work in the United States without requiring sponsorship. We are unable to provide work visa sponsorship or employment authorization for this position now or in the future.

Knowledge Skills and Abilities:

• Ability to communicate effectively both in writing and orally.

• Ability to establish and maintain effective working relationships with employees at all levels throughout the institution.

• Outstanding customer service skills.

• Demonstrated commitment and leadership ability to advance diversity and inclusion.

• Advanced knowledge and understanding of federal regulations and Good Clinical Practice (GCP)

• Knowledge of basic human anatomy physiology medical terminology

• Ability to interpret and master complex research protocol information

• (SME) Expert level knowledge of clinical research processes.

How to Apply:

For full consideration please submit the following document(s):

1. A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position

2. Curriculum vitae / Resume

3. Three to five professional references including name address phone number (mobile number if appropriate) and email address

Questions should be directed to: Jacky Bonds

Screening of Applications Begins:

Immediately and continues until position is filled. For best consideration apply by 2 weeks from posting date.

Anticipated Pay Range:

The starting salary range (or hiring range) for this position has been established as $70446 - $89607.

The above salary range (or hiring range) represents the Universitys good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation depending on the level.

Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave health plans and retirement contributions that add to your bottom line.

Total Compensation Calculator

Equal Employment Opportunity Statement:

CU is an Equal Opportunity Employer and complies with all applicable federal state and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity and we encourage individuals from all backgrounds to apply including protected veterans and individuals with disabilities.

ADA Statement:

The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act please contact the Human Resources ADA Coordinator at .

Background Check Statement:

The University of Colorado Anschutz is dedicated to ensuring a safe and secure environment for our faculty staff students and visitors. To assist in achieving that goal we conduct background investigations for all prospective employees.

Vaccination Statement:

CU Anschutz strongly encourages vaccination against the COVID-19 virus and othervaccine preventable diseases. If you work visit or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work visit or volunteer addition if you work in certain research areas or perform certain safety sensitive job duties you must enroll in theoccupational health medical surveillance program.