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Clinical Research Coordinator

West Cancer Center

Salary not specified
Aug 13, 2025
Memphis, TN, US
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The organization needs a Clinical Research Coordinator to manage oncology patients participating in pharmaceutical sponsored clinical trials.

Requirements

  • RN certification preferred
  • Must be proficient in computer applications including word processing and email
  • Ability to read, analyze and interpret financial reports, government regulations, common scientific and technical journals and legal documents
  • Ability to calculate figures and amounts such as discounts, interest, commissions, percentages, BSA, ANC, drug calculations, area, circumference, and volume
  • Ability to apply concepts of basic algebra and geometry
  • Ability to define problems, collect data, establish facts, draw valid conclusions
  • Ability to interpret an extensive variety of technical complex instructions and deal with several abstract and concrete variables

Responsibilities

  • Recruits subjects for clinical trials through a variety of methods
  • Screens potential subjects for eligibility to clinical trials including a careful review of the patient’s past medical history and a review of current findings
  • Educates staff nurses about proper administration and expected side effects of protocol therapy
  • Educates patients about protocol therapy including when medications are to be taken, what side effects to look for and actions to take in event that side effects occur
  • Reviews newly-activated protocols, amendments, notices, suspensions and terminations
  • Interfaces with Physicians, Physician Nurses, Chemotherapy Nurses, Radiology, Medical Records, Front Desk/Scheduling, Phlebotomy, Laboratory, Insurance and Pharmacy regarding research
  • Maintains a current knowledge of the Code of Federal Regulations

Other

  • Associates degree or equivalent from two-year college or technical school; or a minimum of 1-2 years related experience and/or training; or equivalent combination of education and clinical experience: or must have successfully completed 1 year as an Associate Clinical Research Coordinator 1
  • Must have excellent organization and follow-up skills
  • Must have excellent verbal and written communication skills
  • Must have excellent problem-solving skills; ability to organize and prioritize work assignments
  • Ability to handle multiple priorities in a fast-paced environment
  • Ability to analyze situations and respond in a timely manner
  • Ability to participate in multi-functional teams
  • Ability to establish and maintain effective working relationships within the West Cancer Center
  • Ability to work near toxic or caustic chemicals
  • Ability to sit, stand, walk, reach, climb or balance, stoop or crouch, hand/wrist use, talk, see and hear for extended periods of time
  • Ability to lift up to 10 lbs.
  • Additional hours may be required
  • Travel may be required