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 in the oncology space.
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 in meetings and discussions with site managers and investigators
- Support country budget development and contract negotiation
- Assist with adverse event reporting and metrics/KPIs
- Bachelor's degree in a biological science 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/risk-based monitoring experience is an asset
- Ability to drive patient recruitment strategies and partner with investigators and site staff
- 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
- Willingness to travel up to 50%
We offer a competitive salary and a range of benefits, including annual leave entitlements, health insurance, retirement planning, and a global employee assistance program. We are committed to diversity, inclusion, and belonging and strive to create a workplace free of discrimination and harassment.
At ICON, we value our employees and offer opportunities for growth and development. If you are a motivated and experienced Clinical Research Associate looking for a new challenge, we encourage you to apply.
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