healthcare
Posted 4 hours agoSenior Clinical Trial Manager
at Natera
United StatesRemote
Responsibilities
- Manage study contracting, budget and payment process for all clinical trial vendors including investigational sites. •
- Design study related documents, including but not limited to study protocol, informed consent forms, CRFs, and regulatory binders. •
- Train CROs, vendors, investigators and study coordinators on study protocol and relevant requirement. •
- Monitor and track clinical trial progress and provide status update to stakeholders. •
- Mentor junior clinical operations staff and supervise clinical study team. •
Requirements
- experience in managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management.
- Must maintain a current status on Natera training requirements.
- Bachelor’s degree in life sciences, or other relevant discipline required, Advanced degree preferred. •
- experience in managing clinical trials as a leading role. •
- Experience in managing studies, CROs and sponsors is preferred. •
- Proficiency in MS Word, Excel and PowerPoint •
- Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health.
Experience
- 5-8 years of clinical research experience, including at least 2-5 years of
Benefits
- The pay range is listed and actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location.
- Remote USA $131,900 — $164,900 USD OUR OPPORTUNITY
- Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.