
Clinical Trial Manager
This role also assures adherence to GCP, regulations and applicable procedures, in addition to protocol compliance and that of study related plans. The CTM will also be responsible for monitoring all phases of clinical studies, as needed. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents for global regions (e.g., EU, APAC, China). Develops strong vendor and site relationships and ensures continuity of relationships through all phases of the trial. Participates & provides input on study site selection activities. Performs timely review of monitoring reports and associated deliverables demonstrating sponsor oversight.
5 years of direct site management (monitoring) experience
3-5 years study oversight as an in-house CTM (e.g., CRO/vendor oversight)
Documentation
Vendor Management
Time Management
MS Excel
Negotiation skills
Presentation skills
MS Word
MS PowerPoint
Adaptable
Multitasking
Process Improvement
Verbal communication
written communication
According to JobzMall, the average salary range for a Clinical Trial Manager in 6310 Nancy Ridge Dr, San Diego, CA 92121, USA is between $76,000 and $152,000 per year. This salary range reflects the median salary range for Clinical Trial Managers in the San Diego area. Salaries can vary depending on experience, the size of the company, and other factors.
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Cidara is a clinical-stage biotechnology company focused on developing new anti-infectives that have the potential to transform the standard of care and save or improve patients’ lives. Cidara also leverages the novel Cloudbreak™ platform to develop antibody-drug conjugates for treatment of serious viral and Gram-negative bacterial infections.

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