
Clinical Trials Manager
2 days ago
Are you looking for a challenging role where you can utilize your expertise in clinical trials to drive innovation and excellence? Do you have a passion for working independently and managing complex projects?
We are seeking an experienced Clinical Research Associate II to join our team. As a CRA II, you will be responsible for independently managing all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
Your primary focus will be on ensuring compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements. You will also be responsible for building strong site relationships, acting as a primary point of contact, and ensuring high-quality data collection.
In this role, you will identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety. You will also be involved in activities around regulatory affairs, site activation, and study-startup.
- Lead monitoring activities in complex trials, ideally in oncology or rare disease.
- Have a strong understanding of ICH-GCP and regulatory guidelines.
- Be a clear and confident communicator in English.
- Be comfortable working independently and managing priorities.
Benefits:
- Competitive salary and comprehensive benefits package
- Departmental study/training for furthering professional development
- Mentoring opportunities
- Internal growth opportunities and career progression
About the Role:
This is an exciting opportunity for an experienced CRA to take on new challenges and contribute to the success of our organization. If you are passionate about clinical trials and have a proven track record of success, we encourage you to apply.
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