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Manager-Accessioning

Caris Life Sciences

  • Phoenix, Arizona
  • 8 days ago

    Highlights

    Works cross-functionally with various departments including Customer Support, Supply Chain, Molecular Leaders, Field Team, Software, Automation, Privacy, Clinical Research, and Billing. May have exposure to blood-borne pathogens, extreme temperatures, high noise levels, fumes and bio-hazardous material/chemicals including formalin in the lab environment.

    Numbers & Facts

    LocationPhoenix, Arizona
    IndustryBiotechnology/Pharmaceuticals
    Company Size100 to 499 employees
    Year Founded1996
    Websitehttp://www.carislifesciences.com/

    Description

    At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives.

     

    We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day: “What would I do if this patient were my mom?” That question drives everything we do.

     

    But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a revolution in healthcare—driven by innovation, compassion, and purpose.

     

    Join us in our mission to improve the human condition across multiple diseases. If you're passionate about meaningful work and want to be part of something bigger than yourself, Caris is where your impact begins.

    Position Summary

    The Manager – Accessioning is responsible for overseeing all clerical and ancillary duties, ensuring that case workflow is operating consistently, and troubleshooting issues that may arise. They have direct line supervision of all Accessioning Supervisors, managing employee schedules and training, as well as resolving any professional conflicts that may arise. The Manager manages specimen turn-around times and communicates directly with Management regarding exceptions, timelines, etc. They are also responsible for managing all regulatory activities, enforcing consistent adherence
    to required regulatory guidelines to ensure the highest quality and consistency of services. While maintaining job functions, the Manager - Accessioning also interacts with other departments to ensure an optimal case flow is consistently achieved and all standard laboratory procedures and policies are followed.

    Job Responsibilities

    • Manages all Accessioning Supervisors and oversees all case workflow activities.

    • Adheres to the laboratory's quality control policies, documents all quality control activities, instrument and procedural calibrations and maintenance performed.

    • Follows the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable level of performance.

    • Documents all corrective action taken when a system deviates from the laboratory's established performance specifications.

    • Assists with the tracking, accumulation, and computation of performance metrics.

    • Ensures Accessioning has adequate inventories of supplies.

    • Resolves employee relations issues and recommends disciplinary action when required in partnership with Human Resources.

    • Acts as first point of contact on questions. Keeps team informed of new processes and general updates.

    • Assists to perform other related duties and special projects to support other departments as required.

    • Understands Accessioning protocols as set forth by Lab Management team; communicates questions/clarifies uncertainties.

    • Actively engages leadership for instruction and growth.

    • Assists in the cleaning and maintenance of the Laboratory and Accessioning work space and applicable equipment/resources.

    • Consistently exhibits a professional demeanor in the workplace and works to maintain positive relationships with peers and management.

    • Responsible for filing, tracking, retrieval, and accurate record keeping.

    • Maintains pre-analytic diagnostic viability of all specimens and ensures correct patient labeling of all materials per SOPs.

    • Logs appropriate information into the Laboratory Information System (LIS) and other logs as necessary.

    • Responsible for Quality Assurance (QA)/Quality Control (QC) of cases moving through the laboratory.

    • Develops new protocols and SOPs to address problems and improve quality and safety within Accessioning.

    • Responsible for initiating change controls and presenting at associated meetings.

    • Works cross-functionally with various departments including Customer Support, Supply Chain, Molecular Leaders, Field Team, Software, Automation, Privacy, Clinical Research, and Billing.

    • Initiates and leads pre-analytic performance improvement projects

    • Effectively manages complex cross-functional operational activities within and outside the lab with a high degree of independence and strong managerial judgment.

    • Manages/Assists in the training of new-hires and peers.

    • Proficient in troubleshooting problems and successfully maintains workflow in the lab.

    • Is consistently viewed by teammates, supervisors and management as professional, positive, solution-oriented and a leader within the Laboratory Operations Department.

    • Actively participates in department recruitment activities.

    • Drives scalability through automated software and hardware solutions in partnership with leadership and automation.

    • Leads pre-analytic clinical and pharma research efforts to align with clinical workflows.

    • Drives software solutions in new systems to align with analytical workflows and intake teams.

    • Accepts other duties as assigned.

    Required Qualifications 

    • High School diploma or equivalent required

    • 3+ years of experience in general laboratory operations.

    • 1 year of leadership experience

    Preferred Qualifications 

    • Bachelor’s degree in a scientific discipline

    • 2 years of leaderships experience in high-volume reference laboratory setting.

    Physical Demands

    • Must possess ability to sit, stand, and/or work at a computer for long periods of time.

    • May have exposure to blood-borne pathogens, extreme temperatures, high noise levels, fumes and bio-hazardous material/chemicals including formalin in the lab environment.

    • Visual acuity and analytical skill to distinguish fine detail. Ability to pass a visual color discrimination test.

    • Must possess ability to perform repetitive motion.

    • Ability to lift up to 30 pounds.

    Training 

    • All job specific, safety, and compliance training are assigned based on the job functions associated with this employee. 

    Other

    • This position requires periodic travel and some evenings, weekends and/or Holidays.

    Conditions of Employment:  Individual must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and reference verification.

    This job description reflects management’s assignment of essential functions. Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

     

    Caris Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

    About Company

    Caris Life Sciences® is a leading biotechnology company focused on fulfilling the promise of precision medicine through quality and innovation. Caris Molecular Intelligence®, the company’s healthcare information and comprehensive tumor profiling service with more than 70,000 patients profiled, provides oncologists with the most clinically actionable treatment options available to personalize cancer care today. Using a variety of advanced profiling technologies to assess relevant biological changes in each patient’s tumor, Caris Molecular Intelligence connects biomarker data generated from a tumor with biomarker-drug associations supported by evidence in the relevant clinical literature. The company is also developing its ADAPT Biotargeting System™ technology, a revolutionary and proprietary blood-based platform for the development of novel therapeutics, drug delivery and drug target identification. The platform is also being developed for diagnosis, prognosis, and theranosis of cancer and other complex diseases.

    Caris also maintains the Center of Excellence Network for Precision Medicine (“COE Network”) which was established to promote the appropriate study and use of molecular profiling in the diagnosis and treatment of cancer with leading cancer centers in the United States. Headquartered in the Dallas-Fort Worth Metroplex, Caris Life Sciences offers services throughout Europe, the U.S., Australia and other international markets.

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