ICON plc este o organizație globală de cercetare în regim contractual, care deservește industriile din domeniul sănătății și farmaceutic. Activitatea sa cuprinde servicii clinice, de consultanță și comerciale care sprijină dezvoltarea medicamentelor, de la cercetarea timpurie până la activitățile post-comercializare. Compania oferă soluții precum studii clinice descentralizate, evaluarea siguranței cardiace, laboratoare clinice pentru etapele timpurii, imagistică medicală, informații de reglementare și dovezi din lumea reală. ICON plc dispune, de asemenea, de expertiză terapeutică în domenii precum bolile cardiovasculare, oncologia, medicina internă, terapiile celulare și genice și medicamentele biosimilare, combinând analiza datelor cu o abordare axată pe pacienți pentru a contribui la avansarea programelor clinice.
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.
Descriere
- 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
Cerințe
- 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
Beneficii
- 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