- Bachelor's degree in science or health care related field.
- Must have research certification such as Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or other related research certification.
- Four years of clinical research experience. Relevant experience may be substituted for direct clinical research experience.
- A minimum of two years oncology experience required. Medical/Nursing school training may be substituted for clinical/oncology experience.
- Masters or higher degree in life sciences or healthcare field
- Must be proficient in medical terminology.
- Ability to effectively manage competing priorities and deadlines
- Superb attention to detail skills and excellent organizational skills.
- Demonstrated ability to work independently and collaboratively.
- Professional knowledge of anatomy, physiology, pathology and pharmacology concepts as they relate to oncology patients.
- Must have clinical background and knowledge.
- Previous experience working in health-care and customer service related settings.
- Knowledge of clinical research databases and software.
- Experience with Electronic Medical Record charting.
- Strong communication and interpersonal skills as evidence by application materials.
- Experience adhering to guidelines regarding transparent and honest reporting of confidential and sensitive patient information.
- Proficiency in PC operations and software applications such as MS Outlook, Windows, Excel and Word
- Serves as a clinical operations contact for cell and gene therapy trials with internal and external stakeholders. Works with the Site Development and Project Management teams to conduct feasibility and Pre-Site Selection Visits, assess and develop Cell and Gene portfolio for Cancer and Non-Cancer diagnosis, Disease Working Group oversight in conjunction with Cancer Project Manager, workflow policies and procedures, as needed to meet goals.
- Tracks all study startup procedures for new cell and gene therapy studies proposed to the Cancer Center, startup committee review, including regulatory, budget and contract aspects. Ensure timelines are measured and deliverables are met as applicable.
- Reviews protocols with clinical teams to determine resource type. Support research teams in identifying logistics, priorities and resources of cell and gene trials by assisting in drafting workflows and applicable documents. Ensure potential study risks are escalated to the attention of leadership when appropriate.
- Develops working practice guidelines and processes for the conduction of study procedures in collaboration with multiple disciplines as applicable. Develops communication plans to research and clinical teams related to cell and gene therapy trials.
- Manages the Cell and Gene Therapy Disease Working Group by preparing agendas and facilitating meetings, and reports.
- Manages and/or assist in study pipeline and prepare and present prospective trials to the Executive Review Committee (ERC). Actively participate in Project Management, Site Development, Departmental, Coordinator, Team and Staff meetings as applicable.
- Support upper management through the use of effective tracking tools to provide consistent and accurate project status. Participate in Ad hoc projects as assigned.
- 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.
- Resume/CV AND Cover Letter
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Project Manager, Cell Therapy- Cancer Center - Kansas City, United States - University of Kansas Medical Center
Description
Department:SOM KC Cancer Center Clinical Trials
Clinical Trials Project ManagementPosition Title:
Project Manager, Cell Therapy- Cancer CenterJob Family Group:
Professional StaffJob Description Summary:
Job Description:
The Project Manager manages cell and gene therapy clinical trial portfolio overseen by the Cancer Center. Responsible for overseeing administrative aspects of cell and gene therapy clinical trials from initial trial intake through closeout. This position will develop and oversee processes of the cell and gene therapy trial program specific requirements, reporting and resource development across multidisciplinary teams.
The Project Manager ensures that all clinical and departmental operations are conducted according to the mission of the Cancer Center and University of Kansas Medical Center to achieve excellence in clinical activities in the delivery of patient care and services.
The University of Kansas Cancer Center is the only National Cancer Institute designated Comprehensive Cancer Center in the region, 1 of only 57 in the nation to receive this distinction. Patients gain access to the most promising therapies, cutting-edge clinical trials and world class research.
Condition of employment:
Must maintain research certification during employment, such as Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) or other related certification.
Required Qualifications
Education and Certification:
Education:
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.
Employee Type:
RegularTime Type:
Full timeRate 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:
$75, $115,000.00
Minimum
$75,000.00
Midpoint
$95,000.00
Maximum
$115,000.00
