3 days ago
🇺🇸 United States – Remote
🏄 California – Remote
💵 $140k - $174k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
• Responsible for managing the execution of clinical studies and data collection. • Oversee the review, monitoring, and adherence to clinical protocols. • Interact internally and externally with members of the cross-functional study team. • Supervise more junior CTMs and Associate CTMs as required. • Provide oversight of clinical research studies across all functional areas of the drug development process. • Coordinate and lead study team meetings and provide key stakeholders with updates on study progress.
• Bachelor’s degree required, preferably in a scientific discipline. • Minimum of 8 years of prior clinical operations experience managing clinical trials, preferably with CRO/small biotech experience. • At least 5 years in a supervisory role. • Experience managing early phase studies is preferred. • Must be able to travel up to 10% of the time. • Proficiency with Microsoft Office suite of software, electronic TMF systems, IRT, and EDC systems. • Excellent understanding of the drug development process. • Effective verbal and written communication skills. • Ability to handle multiple tasks to meet deadlines in a dynamic environment. • Experience in rare diseases and/or oncology is preferred.
• Discretionary annual target bonus • Stock options • ESPP • 401k match • Health insurance plans including medical, dental, vision • Basic life insurance • 20 days of PTO • 10 paid holidays • Winter company shutdown
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