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Medical Assistant Oncology Research

MCKESSON

Nashville, Tennessee, U.S.
Full-time, Part-time, Contract, Regular, Temporary
Posted Dec 11, 2025
Onsite

Compensation

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About the role

As the Phlebotomist/Research Care Associate you will draw blood and other related clinical duties for patients enrolled on clinical trials.

Responsibilities

  • draw blood and other related clinical duties for patients enrolled on clinical trials
  • access, flush, and de-access ports
  • perform peripheral and port lab draws
  • obtain blood and other samples, vital signs, and EKGs from patients
  • prepare study supplies/source documents necessary for obtaining lab samples prior to patient treatment
  • utilize electronic medical record (EMR) for source documentation
  • verify of all prepared lab kits against EMR
  • report all known regimen issues to the Protocol Excellence team for correction
  • assist in Sarah Cannon Research Institute Oncology Partners (SCRI OP) Infusion Room with collection of blood and other samples, vital signs, and EKGs from patients
  • assist physicians with procedures, as needed
  • assist patients with activities of daily living (ADLs), as needed
  • perform buccal swabs on pharmacokinetics (PK) patients
  • be responsible for collection of all pharmacokinetic blood draws on patients in the hospital
  • complete and submit FMLA paperwork
  • perform Guardant 360, Myriad, and Tempus collections and complete all necessary paperwork for submission
  • ship these tests
  • be responsible for delivering STAT labs to the CMC laboratory for processing
  • track and document tumor lesion photos for all required patients
  • respond to queries generated from study sponsor and contract lab regarding patient/sample data
  • interface with SCRI OP and CMC laboratory colleagues regarding labs for research patients
  • ensure that all research patients have correct lab kits prior to patients’ visits

Requirements

  • High school diploma, preferably a Technical School Certification in phlebotomy/lab
  • Knowledge of OSHA requirements for safe handling of blood and bodily fluids
  • Knowledge of HIPAA
  • Experience with venipuncture and Blood Processing
  • Experience with EKG Collections
  • Experience with port Accessing, Flushing, and De-Accessing
  • Experience in research is preferred
  • Current BLS Certification

Benefits

  • 401k matching
  • Health insurance
  • Flight privileges

About the Company

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.

Job Details

Salary Range

Salary not disclosed

Location

Nashville, Tennessee, U.S.

Employment Type

Full-time, Part-time, Contract, Regular, Temporary

Original Posting

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