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Medical Research Associate/Phlebotomist

Icon
ICON
1-2 years
Not Disclosed
San Antonio, United States
10 Feb. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Medical Research Associate / Phlebotomist – Clinical Research | San Antonio, TX | Full-Time (On-Site)

Job ID: JR142782
Location: San Antonio, Texas (100% On-Site)
Department: ICON Full Service & Corporate Support – Clinical Research
Employment Type: Full-Time / Permanent
Shift: Sunday to Wednesday | 6:00 AM – 4:30 PM

ThePharmaDaily.com is featuring a career opportunity for a Medical Research Associate / Phlebotomist with ICON in San Antonio, Texas. This on-site clinical research role is ideal for certified Medical Assistants, Phlebotomy Technicians, CNAs, EMTs, Paramedics, or LVNs seeking hands-on experience in clinical trials and patient-focused research operations.

This position combines clinical skills with research coordination, supporting the execution of early-phase and clinical development studies in a controlled research clinic environment.

Role Overview

The Medical Research Associate (MRA) plays a vital role in supporting clinical trial execution, patient procedures, biological sample collection, and research documentation. The position requires strong phlebotomy skills, attention to detail, and the ability to work in compliance with clinical research protocols, regulatory standards, and Good Clinical Practice (GCP) guidelines.

This role is critical in ensuring accurate data collection, protocol adherence, and participant safety throughout the clinical trial process.

Key Responsibilities

  • Perform phlebotomy and assist with clinical procedures in accordance with study protocols.

  • Support the execution of clinical trials, including patient visits, sample collection, and data documentation.

  • Maintain accurate and organized research records to ensure regulatory compliance and audit readiness.

  • Assist with data entry, documentation review, and quality control activities.

  • Collaborate with clinical research coordinators, investigators, and cross-functional teams to meet study timelines.

  • Ensure adherence to ethical standards, safety procedures, and protocol-specific requirements.

  • Support preparation of study-related reports and documentation as required.

Experience Required

  • Minimum 1–2 years of hands-on clinical experience in a healthcare or clinical research setting preferred.

  • Practical experience in phlebotomy and patient care procedures required.

  • Prior exposure to clinical trials or research environments is highly advantageous.

  • Understanding of medical documentation standards and regulatory compliance preferred.

Educational & Certification Requirements

  • High School Diploma or equivalent required.

  • Medical Assistant certification, Phlebotomy Technician certification, CNA, EMT, Paramedic, or LVN credentials preferred.

  • Formal medical assistant or allied health training required.

Core Competencies

  • Strong phlebotomy and patient care skills

  • Attention to detail in clinical documentation and data collection

  • Knowledge of clinical research processes and GCP principles

  • Effective time management and organizational skills

  • Strong communication and teamwork abilities

  • Ability to work in a fast-paced clinical research environment

Why This Opportunity is Valuable for Clinical Professionals

  • Direct involvement in clinical trial operations and patient-facing research activities

  • Fixed weekday shift schedule (Sunday–Wednesday)

  • Exposure to innovative treatments and clinical development programs

  • Competitive compensation and comprehensive benefits package

  • Health insurance, retirement planning, life assurance, and employee assistance programs

  • Professional development within a globally recognized clinical research organization

This role is ideal for professionals seeking to transition into or advance within clinical research, clinical trial operations, or pharmaceutical development environments.