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You will be updated with latest job alerts via email$ 58656 - 86000
1 Vacancy
Key Roles and Responsibilities:
Serve as the Portfolio Manager for clinical trials in assigned disease group area(s) supporting the progress of startup activities and processes related to study activation conduct and closeout. Along with the lead (local) administrator/study team serves as an initial point of contact for new studies.
Coordinate scheduling of startup meetings and facilitate the conduct of feasibility review for new studies; document meeting outcomes and next steps.
Assist study teams to navigate and obtain needed information and services from ancillary units and regulatory committees as appropriate e.g. CTSUs IDS Conflict of Interest Committee Institutional Biosafety Committee etc.
Assist study teams with editorial assistance regarding informed consent forms.
Assist PIs study coordinators and other research staff with problem solving related to clinical logistical financial and regulatory issues.
Monitor the status of startup timelines for new studies including IRB approval and contract execution and the progress of ongoing studies including enrollment. Identify barriers to study activation and enrollment and identify appropriate interventions.
Assure that all tasks necessary for study activation have been completed and communicate with study teams and others regarding the activation process.
Monitor study progress and assist study teams in understanding applicable requirements; participate in department planning meetings where appropriate and facilitate connections with strategic partners and resources as applicable; serve as a conduit of information and provide assigned study teams with access to training resources.
Required Qualifications
Education:
Bachelors degree in a scientific discipline life sciences of healthrelated field. An equivalent combination of education and related work experience may be substituted for degree on a year for year basis.
Work Experience:
Experience working within a clinical research environment and/or supporting the conduct of clinical trials.
Basic understanding of clinical research and applicable federal regulations.
Excellent communication to write clearly and concisely as evidenced by application materials.
Preferred Qualifications
Work Experience:
Prior exposure working with institutional review boards (IRBs) or ethics committees.
Prior experience working within an academic medical center environment.
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 Documents:
Resume/CV
Cover Letter
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. Employerpaid life insurance longterm 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:
Manager
Full-Time