Part Time Medical Research Associate

ICON plc • Lenexa, KS

5d • Onsite

About The Position

ICON is a global healthcare intelligence and clinical research organisation focused on bringing new medicines and treatments to patients faster. The Medical Research Associate (MRA) serves as an early point of contact for participants enrolled in clinical research studies, working with research volunteers during clinic visits to support a positive participant experience and the safe, efficient execution of clinical trials. The role primarily supports evening and overnight operations.

The MRA supports participants throughout the clinical trial process while ensuring compliance with study protocols, regulatory requirements, and participant safety standards. This includes screening and enrollment support, informed consent, protocol-required clinical procedures, accurate documentation, and collaboration with clinical teams.

ICON describes integrity, collaboration, agility, and inclusion as values that guide its work. It is an equal opportunity employer committed to an inclusive and accessible workplace.

Requirements

• High school diploma or GED.
• Strong interpersonal and communication skills to interact professionally with research participants and study staff.
• Ability to accurately collect, document, and review participant information and clinical data.
• Strong attention to detail and organizational skills.
• Ability to work independently and as part of a multidisciplinary team.
• Flexibility to work evening and overnight shifts.
• Legal right to work in the country where the role is based.

Nice To Haves

• Associate's or bachelor's degree in a healthcare, biology, or science-related field.
• Previous experience in a clinical, healthcare, laboratory, or research environment.
• At least 1 year of experience in a medical or clinical setting.
• Basic Life Support (BLS), Certified Phlebotomy Technician, or other relevant clinical certifications.

Responsibilities

• Serve as a primary point of contact for research participants during clinic visits.
• Review medical histories and collect participant information to support study screening and enrollment activities.
• Facilitate and witness the informed consent process, ensuring participants understand study requirements and procedures.
• Perform protocol-required clinical procedures, including vital signs collection, height, weight, BMI measurements, specimen collection, and phlebotomy.
• Accurately document participant data and maintain study records in accordance with study protocols and Good Clinical Practice (GCP) guidelines.
• Explain study procedures and schedules to participants, answer questions, and support a positive research experience.
• Assist clinical teams during dosing days, including participant preparation, monitoring, and study-related procedures.
• Support participant safety through observation, communication, and escalation of concerns when appropriate.
• Collaborate with nurses, physicians, and study teams to ensure protocol compliance and efficient study execution.
• Participate in evening and overnight clinical operations as required.

Benefits

• Competitive base salary and performance-related incentives.
• Health and wellbeing programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programs and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.

What This Job Offers

• Job Type: Part-time
• Education Level: High school or GED