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ICON plc yra pasaulinė sutartinių tyrimų organizacija, teikianti paslaugas sveikatos priežiūros ir farmacijos sektoriams. Jos veikla apima klinikines, konsultavimo ir komercines paslaugas, padedančias vykdyti vaistų kūrimą nuo ankstyvųjų tyrimų iki veiklos po pateikimo į rinką. Įmonė teikia decentralizuotų klinikinių tyrimų, širdies saugumo vertinimo, ankstyvosios klinikinės laboratorinės veiklos, medicininio vaizdinimo, reguliacinės žvalgybos ir realaus pasaulio įrodymų sprendimus. ICON plc taip pat turi terapinių sričių kompetencijos, įskaitant širdies ir kraujagyslių ligas, onkologiją, vidaus ligas, ląstelių ir genų terapijas bei biologiškai panašius vaistus. Derindama duomenų analizę su į pacientą orientuotais metodais, įmonė padeda plėtoti klinikines programas.
Senior Clinical Research Associate – Quebec Remote | ICON plc
Monitor cardiovascular and respiratory clinical trials across Quebec for ICON plc, supporting site compliance, data quality, and adherence to study protocols.
Aprašymas
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead monitoring work with an emphasis on quality and ongoing process improvement
- Evaluate site compliance with protocols, regulations, and Good Clinical Practice requirements
- Perform site visits to review performance, address issues, and support effective study delivery
- Work with cross-functional teams to coordinate accurate, timely data collection and reporting
- Train and advise site personnel and fellow Clinical Research Associates
- Develop and sustain effective working relationships with site teams and study stakeholders
- Monitor cardiovascular and respiratory studies conducted in Quebec
Reikalavimai
- Bachelor’s degree in a relevant scientific or healthcare-related discipline
- Extensive Clinical Research Associate experience, including a strong command of clinical trial processes and regulatory obligations
- Demonstrated ability to oversee multiple sites and projects concurrently, with strong organization and problem-solving skills
- Advanced knowledge of monitoring methods, data integrity, and site management, plus proficiency with applicable clinical trial systems and tools
- Strong communication, interpersonal, and stakeholder-management capabilities, including the ability to promote compliance in a complex setting
- Availability to travel as needed, approximately 60% of the time
- Legal authorization to work in the country where the position is located
Privalumai
- Base salary with performance-based incentives
- Health and wellness programs, including medical, dental, and vision coverage where applicable
- Retirement and pension programs
- Life insurance and disability protection
- Employee assistance programs and wellbeing support resources
- Professional development through structured training and career progression pathways
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