Clinical Research Associate
Behavioral Health Market Context
Apply Nowvia NCBiotech Career Center
Benefits
In addition to your competitive salary, ICON offers a range of additional benefitsOur benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your familyVarious annual leave entitlementsA range of health insurance offerings to suit you and your family’s needsCompetitive retirement planning offerings to maximize savings and plan with confidence for the years aheadGlobal Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-beingLife assuranceFlexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others5 more items(s)
Qualifications
- •Bachelor's degree in a relevant scientific discipline or healthcare-related field
- •Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- •Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
- •Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- •Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment
- •Willingness to travel as required (approximately 60%)
- •Location: East coast
- •4 more items(s)
Responsibilities
- •As a CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
- •You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement
- •Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- •Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution
- •Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting
- •Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct
- •Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations
- •You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others
- •5 more items(s)
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