Manager, Clinical Trials

Natera
United States
Workplace: RemoteFull timeUSD 115,800 - 144,700 annuallyFunction: Laboratory & Clinical OperationsExperience: 8+ yearsEducation: bachelorsSkills: ["Leadership","Communication","Collaboration","Time management","Problem-solving"]

Lead and manage all aspects of complex clinical trials from start-up through close-out, ensuring timelines, budgets, and quality metrics are met and the study complies with protocols and regulatory requirements. Oversee vendor/CRO selection and management, study contracting and budgeting, protocol development, data management collaboration, training, and cross-functional team leadership to deliver high-quality trial results.

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FursaFursa
Natera
Natera
2 months ago

Manager, Clinical Trials

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Source: Company careers pageValidated by: Fursa AI
Last checked: 18 hours agoStatus: Live

Job Summary

Lead and manage all aspects of complex clinical trials from start-up through close-out, ensuring timelines, budgets, and quality metrics are met and the study complies with protocols and regulatory requirements. Oversee vendor/CRO selection and management, study contracting and budgeting, protocol development, data management collaboration, training, and cross-functional team leadership to deliver high-quality trial results.
Location: United States
Workplace: Remote
Employment Type: Full time
Job Function: Laboratory & Clinical Operations

Key Responsibilities

  • •Manage the execution and conduct of all aspects of very complex clinical studies to ensure that timelines, cost, and quality metrics are met.
  • •Responsible for selection of vendors/CROs and provide ongoing management to vendors/CROs to ensure compliance and execution of project deliverables within budget, timeline, and protocol.
  • •Manage study contracting, budget, forecasting, accruals and payment process for all clinical trial vendors including investigational sites.
  • •Lead study-related activities such as protocol and informed consent preparation, investigator selection, study training material development and delivery, monitoring plans development and execution, CRFs, TMF maintenance, protocol amendments, and clinical report preparation.
  • •Collaborate with Clinical Data Management to ensure correct CRF content, create completion guidelines, and design data listings and study reports.

Pay and Benefits

Salary: USD 115,800 - 144,700 annually
Perks:Health InsuranceLife InsuranceDisability401kCommuter BenefitsFertility CarePregnancy Leave

Key Requirements

  • •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 of Clinical Trial SOPs, FDA Regulations, and ICH-GCPs governing the conduct of clinical trials.
Experience:8+ yearsClinical trialsPharmaBiotech
Education:Bachelor's in Life sciences
Skills:LeadershipCommunicationCollaborationTime managementProblem-solving
Languages:English
Tech Stack:MS WordMS ExcelPowerPoint

Company Brief

Natera
Develops and commercializes genetic testing and diagnostics focused on reproductive health, oncology, and organ transplant to inform clinical decision-making and improve patient outcomes.
Industry: Diagnostics
Company Size: Enterprise (1,001+ employees)
Revenue: USD 500M to 1B
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: San Carlos, United States
Founded: 2004
WebsiteLinkedIn