Jobs / Nat***
Clinical Trial Manager
Nat*** · San Carlos, CA, United States
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San Carlos, CA, United States138,600-173,300 USD/yearlyOnsite
Remuneration
138,600-173,300 USD/yearly
Location
San Carlos, CA, United States
Visa sponsorship
Sponsors visa
Job summary
POSITION SUMMARY: The Clinical Trial Manager will be responsible for managing all aspects of clinical trials from start-up through close-out.
Benefits
CompetitiveEmployeeInclude comprehensive medical, dental, vision, life and disability plans for eliAdditionally, Natera employees and their immediate families receive free testingInclude pregnancy and baby bonding leave, 401kCommuterAnd much more.We also offer a generous employee referral program!For more information, visit www.natera.com.Natera is proud to be an Equal Opportunity Employer.Inclusive collaborationOur employees, our community and our patients, and is critical to our mission of
Qualifications
- PRIMARY
- including General Policies and Procedure Compliance and security training.
- Bachelor's degree in life sciences, or other relevant discipline required, Advanced degree preferred.
- 8 years of clinical research experience, including at least 4 years of experience in managing clinical trials as a leading role.
- 4-7 years of experience in supporting clinical trials in a regulated environment .
- Experience in managing CROs is preferred.
- KNOWLEDGE,
Responsibilities
- The Clinical Trial Manager will be responsible for managing all aspects of clinical trials from start-up through close-out.
- Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met
- Works closely with investigative site personnel, CROs, and other study vendors
- Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites
- Collaborate with Clinical Data Management group to ensure correct CRFs content is collected, prepare comprehensive completion guidelines, and design effective data listings and study reports
- Train CROs, vendors, investigators and study coordinators on implementation of study protocol
- Hire, train and oversee Clinical trial staff, and serve as a resource for others within the company for clinical trials management expertise
- Monitor and track clinical trial progress and provide status update to stakeholders
- Support prospective sample testing for studies where Nat*** functions as a central testing facility
- Partner with other research and development groups to create a culture of mutual respect and focus on delivery of high-quality project results
- Hire, train and oversee Clinical trial staff, and mentor junior clinical operations staff.
- Develop Clinical Department SOPs and participate in audits as needed
Skills
CommunicationExcelLeadershipPowerPointWord
Degrees
AssociateBachelorDegree
Industry
EnergyHealthcareMediaPharma
Company size
SmbStartup
Contract length
8 years