drjobs Clinical Research Coordinator Urology

Clinical Research Coordinator Urology

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Kansas City - USA

Monthly Salary drjobs

$ 58656 - 86000

Vacancy

1 Vacancy

Job Description

Department:

SOM KC Urology

-----

Lee Lab

Position Title:

Clinical Research Coordinator - Urology

Job Family Group:

Professional Staff

Job Description Summary:

The Clinical Research Coordinator supports the Department of Urology by coordinating and managing clinical research studies that advance both patient care and scientific discovery in urologic health. Working under the direction of faculty investigators this position plays a key role in recruiting and educating participants ensuring accurate data collection and maintaining compliance with regulatory and institutional standards.

The Coordinator oversees day-to-day study operations including patient monitoring documentation and reporting while collaborating with clinical staff and study sponsors. By integrating research into the departments clinical practice this role directly contributes to improving outcomes for patients with urologic conditions and advancing the departments mission of innovation education and discovery.

Job Description:

Job Responsibilities

  • Recruit evaluates and educate potential patients on clinical trials.

  • Recognize and report adverse events/serious adverse events to the Principal Investigator FDA and sponsors.

  • Perform study procedures as outlined in the protocol and within state and institutional scope of practice.

  • Ensure adequate study supplies are being maintained.

  • Assist clinical staff with phlebotomy and sample collection processing handling and shipping as outlined in the protocol and within institutional/KUMC policy.

  • Coordinate all aspects of study visit activities including scheduling of study visits and hospital-based procedures such as imaging.

  • Maintain source documents and submit case report forms (CRFs) as required for clinical trials.

  • Prepare and submit annual IRB submission.

  • Prepare documentation and participate in study monitoring visits reviews and audits.

  • Facilitate trial activities such as sponsor calls and team meetings.

  • Provide written and verbal reports to Urology Research Manager.

  • Attend strategic planning meetings as requested by manager.

This job description is not designed to cover or contain a comprehensive listing of activities duties or responsibilities that are required of the employee for this job. It is only a summary of the typical functions of the job not an exhaustive list of all possible job responsibilities tasks duties and assignments. Furthermore job duties responsibilities and activities may change at any time with or without notice.

Required Qualifications

Work Experience:

  • 4 years of relevant work experience. Education may be substituted for experience on a year for year basis.

  • Experience with regulations governing clinical research (CFR GCP HIPAA).

  • Experience with statutes and guidelines relevant to regulatory affairs in clinical research.

  • Experience study budgets contracts and grant applications.

Preferred Qualifications

Education: Bachelors degree in relevant field.

Certifications/Licenses: Research certification preferred such as:

  • Certified Clinical Research Coordinator (CCRC)

  • Certified Clinical Research Professional (CCRP)

Skills

  • Communication.

  • Presentation skills.

  • Multi-tasking.

  • Interpersonal skills.

Comprehensive Benefits Package:

Coverage begins on day one for health dental and vision insurance and includes health expense accounts with generous employer contributions if the employee participates in a qualifying health plan. Employer-paid life insurance long-term disability insurance and various additional voluntary insurance plans are available. Paid time off including vacation and sick begins accruing upon hire plus ten paid holidays. One paid discretionary day is available after six months of employment and paid time off for bereavement jury duty military service and parental leave is available after 12 months of employment. A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b) are available. Type: Regular

Time Type:

Full time

Rate Type:

Salary

Compensation Statement:

The pay range listed for this position is determined by our compensation program using market data and salary benchmarking. A combination of factors is considered in making compensation decisions including but not limited to education experience and training qualifications relative to the requirements of the position and funding. At the University of Kansas Medical Center a reasonable estimate for the starting pay range will be the minimum to midpoint of the posted range taking into account the combination of factors listed above.

Pay Range:

$58656.00 - $86000.00

Minimum

$58656.00

Midpoint

$72328.00

Maximum

$86000.00

Required Experience:

IC

Employment Type

Full-Time

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.