Clinical Research Coordinator

Job Summary This position will act as the clinical research coordinator for all projects in the Department of Urologic Surgery. The primary responsibilities of the position will involve day-to-day management of clinical trials in areas of data management, regulatory administration and direct patient contact relating to new and ongoing clinical research within the department. These trials can be both industry-sponsored and investigator-initiated studies. The position requires the use of skills to independently or with general direction coordinates and follow through in the overall administration and outcome of clinical studies. Occasional travel and overtime may be required. Job Summary This position will act as the clinical research coordinator for all projects in the Department of Urologic Surgery. The primary responsibilities of the position will involve day-to-day management of clinical trials in areas of data management, regulatory administration and direct patient contact relating to new and ongoing clinical research within the department. These trials can be both industry-sponsored and investigator-initiated studies. The position requires the use of skills to independently or with general direction coordinates and follow through in the overall administration and outcome of clinical studies. Occasional travel and overtime may be required. Apply By Date 9/11/2026 by 11:59pm Minimum Qualifications - For full consideration, applicants are encouraged to upload license and/or certification if required of the position High school diploma and sufficient experience and demonstrated relevant experience to successfully perform the assigned duties and responsibilities Minimum one year of experience working with study subjects (research participants or patients). Demonstrated experience starting and maintaining clinical trials and research projects according to the requirements of the National Health Institutes of Health, FDA, IRB, Office of Human Research Protection and sponsored guidelines. Demonstrated experience of regulatory process and data management activities. Experience obtaining informed consent from research participants. Demonstrated knowledge of Federal and State regulations for conducting research on human subjects; demonstrated knowledge of Good Clinical Practices for Clinical Research. Knowledge and understanding of basic anatomy and medical terminology. Display organizational skills and attention to detail so that large volumes of records can be accurately maintained and workload priorities can be determined in an appropriate way to accomplish a task or goal. Ability to multi-task. Display writing skills including ability to compose reports and correspondence while utilizing correct grammar, spelling and punctuation as well as clearly documenting research data onto forms. Analytical skills to independently and tactfully assume responsibility for coordination and completion of complex projects requiring interactions with many individuals in a matrix organizational structure. Ability to work with minimal direction and to take the initiative to follow up on projects. Demonstrated experience to exercise professional judgment, use creativity and decision-making to assess situations and needs, define problems, and develop strategies to meet long-range goals to improve processes within the scope of responsibility of the position. Demonstrated excellent oral communication and interpersonal skills to effectively correspond with the general public, co-workers, physicians, patients, caregivers, clinic staff, and other health care professionals. Display tact, diplomacy and flexibility to effectively deal with faculty, staff, agencies and others. Ability to represent the Department in a professional manner. Ability to work effectively and efficiently under pressure despite frequent interruptions, flexibility to adapt to changes and function as a team player. Preferred Qualifications Certification by Society of Clinical Research Associates and/or Association of Clinical Research Professionals highly preferred. Bachelor's degree in a related field such as biology, health science, nursing, public health, or another life science highly preferred Experience reviewing medical records and using an electronic medical record system. Knowledge and understanding of urology and disease processes as applied to clinical research. Knowledge of UCD University policies and guidelines. Key Responsibilities

60% - DATA MANAGEMENT AND COORDINATION

35% - REGULATORY SUPPORT AND ADMINISTRATION

5% - OTHER CLINICAL TRIAL COORDINATION AND ADMINISTRATION Department Overview The Department of Urologic Surgery in the School of Medicine educates medical students, residents, clinical and postdoctoral fellows, conducts both basic science and clinical research, including clinical trials; and provides state-of-the-art clinical care services.

POSITION INFORMATION

Salary or Pay Range: $36.35 - $58.45 Salary Frequency: Hourly Salary Grade: 101 UC Job Title: CLIN RSCH CRD UC Job Code: 009335 Number of Positions: 1 Appointment Type: Staff: Career Percentage of Time: 100% Shift (Work Schedule): Mon-Fri, 8am - 5pm Location: Ellison Ambulatory Care Center (HSP098) Union Representation: RX-Research Professionals Benefits Eligible: Yes This position is 100% on-site Benefits Outstanding benefits and perks are among the many rewards of working for the University of California. UC Davis offers a full range of benefits, resources and programs to help you bring your best self to work, as well as to help you and your family achieve your health, wellness, financial and career goals. Learn more about the benefits below and eligibility by visiting UCnet Benefits Page or Benefits Summary for UC Davis Health Employees or Benefits Summary for UC Davis Employees. High quality and low-cost medical plans to choose from to fit your family's needs UC pays for dental and vision coverage for you and your family Retirement plans for eligible employees including Pension and other Retirement Saving Plans Supplemental insurance offered including additional life, short/long term disability, pet insurance, legal coverage, accident, critical illness and hospital indemnity Pregnancy and Parental Leave, Family & Medical Leave, Adoption Assistance and Pay for Family Care and Bonding for eligible employees Lactation Support Program and Family Care discounts and resources Employee Well-being resources and programming to support thriving in all aspects of employee's lives On-site Employee Assistance Program including access to free mental health services Generous amount of paid Holidays annually as outlined in the UC Policies or Collective Bargaining Agreements Paid Time Off/Vacation/Sick Time as outlined in the UC Policies or Collective Bargaining Agreements Continuing Education (CE) allowance and Staff Education Reimbursement Program for eligible employees Access to free professional development courses and learning opportunities for personal and professional growth Public Service Loan Forgiveness (PSLF) Qualified Employer and Student Loan Debt Counseling Program for eligible employees Physical Demands Standing - Occasional Up to 3 Hours Walking - Occasional Up to 3 Hours Sitting - Continuous 6 to 8+ Hours Lifting/Carrying 0-25 Lbs - Occasional Up to 3 Hours Lifting/Carrying 26-50 lbs - Occasional Up to 3 Hours Lifting/Carrying over 50 lbs - Occasional Up to 3 Hours Pushing/Pulling 0-25 Lbs - Occasional Up to 3 Hours Pushing/Pulling 26-50 lbs - Occasional Up to 3 Hours Pushing/Pulling over 50 lbs - Occasional Up to 3 Hours Bending/Stooping - Occasional Up to 3 Hours Squatting/Kneeling - Occasional Up to 3 Hours Twisting - Occasional Up to 3 Hours Climbing (e.g., stairs or ladders) - Occasional Up to 3 Hours Reaching overhead - Occasional Up to 3 Hours Keyboard use/repetitive motion - Continuous 6 to 8+ Hours Environmental Demands Chemicals, dust, gases, or fumes - Occasional Up to 3 Hours Loud noise levels - Occasional Up to 3 Hours Extreme Temperatures - Occasional Up to 3 Hours Uneven Surfaces or Elevations - Occasional Up to 3 Hours Mental Demands Sustained attention and concentration - Continuous 6 to 8+ Hours Complex problem solving/reasoning - Frequent 3 to 6 Hours Ability to organize & prioritize - Continuous 6 to 8+ Hours Communication skills - Continuous 6 to 8+ Hours Numerical skills - Occasional Up to 3 Hours Constant Interaction - Continuous 6 to 8+ Hours Customer/Patient Contact - Frequent 3 to 6 Hours Multiple Concurrent Tasks - Continuous 6 to 8+ Hours Work Environment UC Davis is a smoke and tobacco free campus effective January 1, 2014. Smoking, the use of smokeless tobacco products, and the use of unregulated nicotine products (e-cigarettes) will be strictly prohibited on any UC Davis owned or leased property, indoors and outdoors, including parking lots and residential space. Must be able to work extra hours to ensure completion of tasks. May require traveling to other UCD locations within the Sacramento Campus as well as Davis Campus. Special Requirements – Please contact your recruiter with questions regarding which activities apply by position This is a critical position, as defined by UC Policy and local procedures, and as such, employment is contingent upon clearing a criminal background check(s) and may include drug screening, medical evaluation clearance and functional capacity assessment This position is designated as a mandated reporter under CANRA and UC policy, and employment is contingent on compliance with applicable policies, procedures and training requirements Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. A Culture of Opportunity and Belonging At UC Davis, we're committed to solving life's most urgent challenges and building a healthier, more resilient world. We believe in growing through every challenge, continually striving to improve, and welcoming new perspectives that strengthen our community. We recognize that a vibrant and innovative organization values both individual strengths and shared purpose. The best ideas often emerge when people with different experiences come together. As you consider joining UC Davis, we invite you to explore our Principles of Community, our Clinical Strategic Plan and strategic vision for research and education. We believe you belong here. The University of California, Davis is an Equal Opportunity Employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status. 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