Senior Medical Research Associate
About The Position
ICON plc is a world-leading clinical research organization. We advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our full-service clinic in Lenexa, Kansas, is a 114-bed, state-of-the-art research center, located near metropolitan Kansas City. We are seeking a Senior Medical Research Associate with active Paramedic licensure to support clinical research studies at our Lenexa, Kansas (KS) clinic. Whether you’re exploring a career in clinical research or already have experience in the field, this role offers a chance to contribute to work that supports the future of healthcare and disease management. Paramedic candidates without research experience are encouraged to apply. The Senior Medical Research Associate opportunity blends patient care with research responsibilities.
Requirements
- Active, unrestricted Paramedic state license.
- National Registry Paramedic (NRP) certification or state‑recognized equivalent.
- Strong understanding of patient assessment, emergency response protocols, and clinical documentation standards.
Nice To Haves
- Paramedic candidates without research experience are encouraged to apply.
Responsibilities
- Provide direct patient care within the onsite clinic, including advanced assessment, triage, vital signs, and urgent clinical support.
- Perform Paramedic‑level procedures within licensure scope, including IV placement, blood draws, specimen collection, injections, wound care, and emergency response/stabilization.
- Monitor participant safety during research procedures and respond promptly to medical concerns, adverse events, or unexpected clinical situations.
- Ensure medical equipment, supplies, and emergency materials are maintained, stocked, and fully operational.
- Assist in planning, coordinating, and executing clinical research activities in alignment with study protocols and regulatory requirements.
- Support study visit procedures, including sample handling, documentation, timing, and protocol‑driven tasks.
- Conduct or support staff training, reinforce protocol adherence, and provide ongoing operational assistance to investigators and team members.
- Track study progress, maintain accurate and audit‑ready documentation, and ensure high‑quality records throughout the study lifecycle.
- Contribute to the development and review of study materials, including source documents, manuals, logs, and operational tools.
Benefits
- Full healthcare benefits
- 401k matching
- generous paid time off (PTO)
- paid holidays
- life insurance
- paid leave
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
No Education Listed
