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Clinical Trials Specialist
3 weeks ago
Clinical Research Associate - Solid Tumor Oncology
Description:We are seeking a highly skilled Clinical Research Associate to join our team in the Central, West or East regions. As a CRA, you will be responsible for monitoring clinical trial sites to ensure adherence to study protocols and regulatory requirements.
You will conduct site visits to assess site performance, resolve issues and provide support to ensure successful trial execution. You will also collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
Your expertise in monitoring practices, data integrity and site management will be essential in this role. You will be working with a range of clinical trial software and tools and must have excellent communication, interpersonal and stakeholder management skills.
Responsibilities:- Monitoring clinical trial sites to ensure adherence to study protocols and regulatory requirements.
- 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.
- 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.
- Located in the Central, West or East regions.
- Minimum of 12 months of independent monitoring experience.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Annual leave entitlements.
- Health insurance offerings.
- Retail savings scheme.
- Global Employee Assistance Programme.
At [Company], we value diversity and inclusion and are committed to creating an inclusive work environment where everyone can thrive. We welcome applications from diverse candidates who share our values.