Natera
Senior Clinical Trial Manager
US Remote · Senior
Sponsorship not specified$132k-$165kDetected 13 hours ago
ComplianceExcelHIPAAClinical TrialsClinical ResearchFDA RegulatoryResearchExperimental DesignLeadershipCommunicationCollaborationAdaptabilityMicrosoft Office
About the role
- The Senior Clinical Trial Manager will be responsible for managing all aspects of clinical trials in the field of Oncology.
- The candidate will work closely with Natera's clinical trials, R&D and scientific communications teams to accomplish this end.
- Responsible for the implementation of clinical trial activities per study protocol.
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.
- Partner with other research and development groups to achieve deliverables.
- This role works with PHI on a regular basis both in paper and electronic form and have an access to various technologies to access PHI (paper and electronic) in order to perform the job.
- Must maintain a current status on Natera training requirements.
- The Clinical Trial Manager should have experience in managing all aspects of the trials independently, including study design, protocol implementation, site monitoring, and recruitment site management.
- Natera is dedicated to robust clinical trial design and execution, as demonstrating test ability and performance is essential to Natera's reputation and integrity.
- Natera takes cyber crimes seriously, and will collaborate with law enforcement authorities to prosecute any related cyber crimes.
Requirements
- 5-8 years of clinical research experience, including at least 2-5 years of experience in managing clinical trials as a leading role.
- Familiar with the FDA regulations relevant to clinical trials.
- Able to collaborate with the study team, cross functional team members and external collaborators
- 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. This may differ in other locations due to cost of labor considerations.
- Remote USA
- $131,900 - $164,900 USD
Nice to have
- Bachelor's degree in life sciences, or other relevant discipline required, Advanced degree preferred.
- Experience in managing studies, CROs and sponsors is preferred.
Skills
- Proficiency in MS Word, Excel and PowerPoint
- Good organization and planning skills
- Strong interpersonal skills and communication skills (both written and oral)
- Strong leadership skills, self-motivated, adaptable to a dynamic and fast paced environment
Compensation
- 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.
Benefits
- Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents.
- Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits.
- Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more.
- Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.
Company info
- We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives.
Equal opportunity
- Equal Opportunity Employer.
This listing is sourced directly from Natera's careers page and normalized into a canonical job model.