ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
Senior Clinical Research Associate, Medical Device — Remote, United States
Senior Clinical Research Associate overseeing orthopedic medical-device trials for ICON Strategic Solutions. The role covers site monitoring, compliance, data integrity, and trial execution across Midwest and Western regions.
United States
Illinois
Missouri
Nebraska
Oklahoma
Texas$110,520 – $138,150 / year
RemoteFull-timeSeniorEnglish RequiredClinical ResearchDescription
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead technically complex monitoring work with an emphasis on quality and ongoing improvement
- Evaluate clinical sites for compliance with protocols, regulations, and Good Clinical Practice standards
- Conduct site visits to review performance, address issues, and support effective study delivery
- Partner with cross-functional teams to ensure clinical data and reports are collected accurately and on schedule
- Train and advise site personnel and fellow Clinical Research Associates
- Develop and sustain effective working relationships with site teams and other stakeholders
- Coordinate multiple clinical sites and projects at the same time
Requirements
- Bachelor’s degree in a relevant scientific or healthcare discipline
- Three to five years of Clinical Research Associate monitoring experience in CRO or pharmaceutical settings
- Demonstrated experience managing complex clinical protocols
- Substantial Clinical Research Associate experience and a strong command of clinical trial processes and regulatory obligations
- Track record of managing several sites and projects concurrently
- Advanced knowledge of monitoring methods, data integrity, and site management
- Working knowledge of applicable clinical trial software and tools
- Strong communication, relationship-building, and stakeholder management abilities
- Availability for approximately 60% travel as required
- Some travel to Canada may be required
- Legal authorization to work in the country where the position is based
Benefits
- Base salary with performance-based incentive opportunities
- Medical, dental, and vision coverage through health and wellbeing programs where applicable
- Retirement and pension arrangements
- Life insurance and disability protection
- Employee assistance programs and wellbeing support resources
- Structured training and career development opportunities