Employer Active
Job Alert
You will be updated with latest job alerts via emailJob Alert
You will be updated with latest job alerts via email$ 58656 - 86000
1 Vacancy
-----
Lee LabJob 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 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. Minimum Midpoint MaximumTime Type:
Full timeRate Type:
SalaryPay Range:
$58656.00 - $86000.00
Required Experience:
IC
Full-Time