Senior CRA
Behavioral Health Market Context
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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 familyOur Benefits Examples IncludeVarious 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, Life Works, 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 others6 more items(s)
Qualifications
- •Advanced degree in a relevant field such as life sciences, nursing, or medicine
- •Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- •Experience in Oncology required
- •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
- •Fluent in German and English
- •Ability to travel at least 60% of the time
- •5 more items(s)
Responsibilities
- •As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards
- •You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle
- •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
- •4 more items(s)
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