ICON
Senior Clinical Research Associate (CRA) role at ICON plc, overseeing clinical trial activities, ensuring data integrity, participant safety, and compliance. Collaborating with cross-functional teams, providing training and guidance to site staff, and building effective relationships with site personnel and stakeholders.
Requirements
- 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.
- 2-3 years of monitoring oncology trials.
- 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.
- Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid driver’s license
Benefits
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
Originally posted on Himalayas
To apply for this job please visit himalayas.app.
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