Clinical Research Associate
3 weeks ago
We are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials within the Oncology department.
Key Responsibilities- Monitor and manage multiple clinical trials within Oncology
- Develop and implement quality control measures to ensure trial integrity
- Collaborate with cross-functional teams to ensure trial success
- Provide training and support to junior team members
- Develop and maintain site start-up documents, including SIV agendas
- Review and provide feedback on study documents, such as Monitoring Guidelines
- Represent the team at SMTs and meetings
- Take on lead roles and responsibilities as needed
- Bachelor's degree in Biological Sciences or equivalent
- Minimum 2-3 years of experience in monitoring pharmaceutical industry clinical trials
- Minimum 1-3 years of experience monitoring Oncology trials
- Knowledge of several therapeutic areas
- Analytical and risk-based monitoring experience is an asset
- Ability to drive patient recruitment strategies at assigned sites
- Ability to partner closely with investigator and site staff to meet study timelines
- Strong communication and influencing skills
- Ability to operate and use various systems and databases
- Knowledge of Good Clinical Practice, ICH guidelines, and local regulatory requirements
- Ability to travel up to 50%
- Competitive salary range: $89,376.00 - $111,720.00 USD
- Annual leave entitlements
- Range of health insurance offerings
- Competitive retirement planning offerings
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
At ICON, we value diversity, inclusion, and belonging. We are committed to providing an inclusive and accessible environment for all candidates. If you need a reasonable accommodation for any part of the application process, please let us know.
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