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Medical Research Associate (Phlebotomist)

Icon Plc
ICON PLC
1+ years
Not Disclosed
Kansas City, Lenexa, Remote
1 May 7, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs

Medical Research Associate (Phlebotomist)

Company: ICON plc
Job Title: Medical Research Associate (Phlebotomist)
Location: Lenexa, Kansas, United States
Work Mode: On-Site
Job Type: Full-Time
Reference ID: JR150219


Job Overview

ICON plc is hiring a Medical Research Associate (Phlebotomist) for its clinical research operations team in Lenexa, Kansas. This role involves supporting clinical trial participants by conducting vital sign assessments, performing phlebotomy procedures, and ensuring study volunteers meet protocol-specific health requirements before participating in clinical research studies.

This opportunity is ideal for candidates with healthcare, laboratory, nursing support, or patient-care experience who want to build a long-term career in the clinical research and pharmaceutical industry.


Experience Required

  • Preferred Experience: Minimum 1+ year in a medical or clinical environment
  • Freshers Eligibility: Freshers with relevant certifications, internships, healthcare training, or clinical exposure may also apply

This role is considered:

  • Entry-Level to Junior-Level Clinical Research Role
  • Suitable for healthcare support professionals entering the CRO/pharma sector

Educational Qualification

Minimum Qualification

  • High School Diploma or G.E.D.

Preferred Qualification

  • Undergraduate degree in:
    • Healthcare
    • Nursing
    • Allied Health Sciences
    • Clinical Sciences
    • Medical Assistance
    • Laboratory Sciences

Preferred Certifications

Candidates with the following certifications will have an advantage:

  • Basic Life Support (BLS)
  • Certified Phlebotomist Certification

Preferred Candidate Backgrounds

ICON highly prefers candidates from:

  • Medical Assistant
  • Certified Nursing Assistant (CNA)
  • Certified Medication Aide
  • Telemetry Technician
  • Laboratory Technician
  • Phlebotomist
  • Clinical Support Associate

Key Responsibilities

Clinical Trial Participant Support

  • Welcome and assist clinical trial volunteers during study visits
  • Ensure participants are comfortable and supported throughout the study process
  • Verify participant readiness according to clinical trial protocols

Vital Signs Assessment

  • Record:
    • Height
    • Weight
    • Blood Pressure
    • BMI
    • Additional protocol-required vitals

Phlebotomy & Sample Collection

  • Perform blood collection and phlebotomy procedures
  • Follow study-specific clinical protocols accurately
  • Maintain patient comfort and safety during procedures

Clinical Operations Support

  • Participate in meetings and study-related operational activities
  • Support research teams with participant coordination
  • Chaperone study participants during scheduled breaks when required

Required Skills

Clinical & Technical Skills

  • Phlebotomy
  • Vital sign monitoring
  • Basic clinical assessments
  • Patient care support
  • Clinical protocol adherence

Soft Skills

  • Strong communication skills
  • Attention to detail
  • Compassionate patient interaction
  • Team collaboration
  • Time management