Senior Laboratory Coordinator (Correlative Lab) Cancer Center

The University of Kansas Health System; Kansas City (MO); On-site; USD 39,000 - 52,000; Full time

Job summary

The University of Kansas Health System is seeking a Senior Laboratory Coordinator to coordinate oncology clinical trial specimens and supplies per protocol, including pharmacokinetics and pharmacogenomics studies.

You will support industry-sponsored and investigator-initiated trials, collaborate with nursing and physicians, manage specimen integrity, and mentor junior staff while traveling between sites as needed.

Qualifications

• 4 years of relevant work experience. Education may be substituted for experience on a year for year basis.
• One year of lab assistance and lab tech experience.
• Previous laboratory clinical trial experience.
• Previous oncology experience.
• Familiarity with medical terminology.

Responsibilities

• Possess an in-depth knowledge of specimen collection, processing, and shipping requirements for protocols within the Clinical Trials Office. Accurately obtain, document, process and manage serial specimens (blood and other bodily fluids) obtained from patients participating in clinical trials.

Skills

Interpersonal skills

Time management

Organization

Attention to detail

Multitasking

Communication

Critical thinking skills

Computer skills

Job description

Department:

SOM KC Cancer Center Clinical Trials

Clinical Research

Position Title:

Senior Laboratory Coordinator (Correlative Lab) Cancer Center

Job Family Group:

Professional Staff

Job Description Summary:

The Senior Laboratory Coordinator will be responsible for coordination of oncology clinical trial study specimens and supplies per protocol requirements. This includes pharmacokinetics, pharmacogenomics and ancillary studies for Industry-Sponsored, Cooperative Group and Investigator Initiated clinical trials.

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.

Job Description:

Job Responsibilities

• Possess an in-depth knowledge of specimen collection, processing, and shipping requirements for protocols within the Clinical Trials Office. Accurately obtain, document, process and manage serial specimens (blood and other bodily fluids) obtained from patients participating in clinical trials.

• Coordinate the collection of central study samples and required study assessments in collaboration with nursing, study coordinators, physicians and patients in a timely manner.

• Responsible for requesting and shipping research related pathology requests for the CTO. Collaborates with Tissue Repository staff and assists with obtaining and shipping tissue specimens based on IATA/DOT Guidelines. Communicate with Study Coordinators regarding the status oftissuerequests.

• Perform study specific ECGs and transmit data to appropriate database as listed in the study protocol schedule of events.

• Assist with training, mentoring, shadowing and onboarding junior staff when directed by management.

• Occasionally travel between the Clinical Research Center, Westwood Facility, Indian Creek Campus and The University of Kansas Health System Hospital for meetings, kit drop off and transport of study specimens.

• Verify accuracy and properly store study flowsheets when directed by management.

• Provide quick and accurate email responses and query resolution to sponsors, monitors, nursing, study coordinators, etc.

• Work with data coordinators during onsite monitor visits and audits to provide organized, accurate patient lab charts. Proactively check-in with study monitors and provide requested lab documents.

• Excellent documentation with limited errors in data collection, entry and sample shipment.

• Attend Kick-Off-Meetings and assist management with Site Initiation Visits when needed.

• Reference and maintain a variety of study protocols and central lab manuals.

• Responsible for Inventory Maintenance of study supplies including, but not limited to, maintaining adequate kit amounts, ensuring the destruction of kits and creation of NTFs, submitting kit supply orders, updating kit inventory spreadsheet, as well as preparing kit orders for Satellite Sites.

• Accurately perform data entry, if necessary, in both Hospital and Laboratory information systems according to hospital and laboratory policies and procedures, as well as compliance requirements.

• Ensure all requirements for specimen integrity have been met (positive patient identification, correct specimen collected, proper transport of samples has been employed, etc.).

• Utilize EMR (Epic) and Outlook lab calendar to set up study lab collections and schedule upcoming couriers.

• Participate in weekly lab rotation, daily patient assignments and Friday handoff emails.

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.

Work Environment

• Medical laboratory environment involving handling of laboratory equipment and samples. Additional work performed in a general office environment.

Required Qualifications

Work Experience:

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

• One year of lab assistance and lab tech experience.

Preferred Qualifications

Work Experience:

• Previous laboratory clinical trial experience.

• Previous oncology experience.

• Familiarity with medical terminology.

Skills

• Interpersonal skills.

• Time management.

• Organization.

• Attention to detail.

• Multitasking.

• Communication.

• Critical thinking skills.

• Computer skills.

Required Documents

• Cover letter

• Resume/CV

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. https://www.kumc.edu/human-resources/benefits.html

Employee Type:

Regular

Time Type:

Full time

Rate Type:

Hourly

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:

$28.20 - $38.35

Minimum

$28.20

Midpoint

$33.17

Maximum

$38.35