Clinical Trial Manager
$140,000 - $170,000
My client, a leading global CRO, is seeking to expand its Clinical Operations team and is in search of an exceptional candidate to join their ranks. We have the privilege of partnering with them to identify top-notch Clinical Trial Management professionals who can contribute to the organization's growth and overall success. As part of a cohesive group of medical experts, you will collaborate to provide therapeutic solutions to patients, enhancing their quality of life and advancing the quest for medical breakthroughs.
- Ensure operational management of assigned project(s) in full compliance with ICH/GCP and relevant regulations.
- Serve as the primary point of contact for sponsors and principal stakeholders regarding project-specific challenges and study deliverables.
- Provide expertise and insight into therapeutic areas for assigned studies.
- Lead and oversee project team members, bridging functional boundaries.
- Responsibilities encompass reviewing study protocols, managing projects, developing SOPs, crafting final study reports, and executing other essential study tasks.
- Develop and implement study management plans.
- Uphold site quality standards by directly supervising Clinical Research Associates on the project and monitoring deliverables.
- Possess a Bachelor's degree in life sciences or a related field.
- Accumulate a minimum of 3 years of experience in clinical trial management.
- Demonstrate proficiency in regulations and GCP guidelines.
- Familiarity with Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems is a plus.
Additional Perks: The company offers an attractive benefits package along with a competitive salary. All applicants must be eligible to work for a US-based employer.