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Senior Oncology Clinical Research Associate
2 months ago
We are seeking a highly skilled Oncology Clinical Research Associate to join our team at ICON Strategic Solutions. As a key member of our clinical research team, you will be responsible for managing multiple oncology trials, with a focus on quality of life and regional travel.
Key Responsibilities- Manage multiple oncology trials, ensuring timely and efficient execution.
- Develop and implement quality of life-focused strategies for trial participants.
- Provide leadership and mentorship to junior team members, promoting a culture of excellence and collaboration.
- Act as a subject matter expert, training and guiding other team members on study protocols and procedures.
- Develop and maintain site startup documents, including SIV agendas.
- Review and provide input on study documents, ensuring compliance with Good Clinical Practice and ICH guidelines.
- Represent the team at local and regional meetings, ensuring effective communication and collaboration with stakeholders.
- Support country budget development and contract negotiation, working closely with CCS colleagues.
- Assist with adverse event reporting and metrics/KPIs, ensuring compliance with quality oversight plans.
- Minimum of 3 years' experience in monitoring pharmaceutical industry clinical trials.
- Minimum of 3+ years' experience monitoring oncology trials.
- Knowledge of several therapeutic areas, with oncology an asset.
- Analytical/risk-based monitoring experience an asset.
- Ability to drive patient recruitment strategies and partner with investigators and site staff to meet study timelines.
- Strong communication and influencing skills, with ability to work independently and as part of a team.
- Good understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements.
- Ability to travel up to 50%.
At ICON Strategic Solutions, 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 that is inclusive and accessible for all candidates.
", "requirements": "Requirements- Minimum of 3 years' experience in monitoring pharmaceutical industry clinical trials.
- Minimum of 3+ years' experience monitoring oncology trials.
- Knowledge of several therapeutic areas, with oncology an asset.
- Analytical/risk-based monitoring experience an asset.
- Ability to drive patient recruitment strategies and partner with investigators and site staff to meet study timelines.
- Strong communication and influencing skills, with ability to work independently and as part of a team.
- Good understanding of Good Clinical Practice, ICH guidelines, and local regulatory requirements.
- Ability to travel up to 50%.
At ICON Strategic Solutions, 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 that is inclusive and accessible for all candidates.
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