Cresilon, Inc.

Cresilon, Inc.

Preclinical Principal Scientist, Research & Development

Brooklyn, New York, United States · Principal

Sponsorship not specified$130k-$210kDetected 45 days ago
ComplianceProject ManagementVendor ManagementGMPFDA RegulatoryMedical DevicesResearchExperimental DesignAnimal StudiesAnimal ModelsLeadershipCommunicationProblem SolvingOrganizational Skills

About the role

  • The company's plant-based technology has revolutionized the current standard by stopping traumatic and surgical bleeds in seconds without the need for extended manual pressure.
  • The company's current and future product lines target veterinary, human trauma, and human surgical applications.
  • Learn more about the company at www.cresilon.com.

Responsibilities

  • The Preclinical Research Scientist will: Lead, staff, and manage Cresilon's Preclinical Research activities.
  • Develop, write, and/or review study protocols and reports.
  • Act as a technical mentor for the development of study experimental designs, protocols, and reports of junior associates.
  • Administrater and manage Cresilon's preclinical regulatory strategy and communication.
  • Actively interact with the internal and external scientific community to maintain state-of-the-art knowledge.
  • Oversee the design and execution of preclinical functionality and safety in-vivo studies per project timelines.
  • Manage budgetary requirements for all research projects to support efficacy and safety programs.
  • Lead the effort to publish surgical research in peer-reviewed journals.
  • Lead, staff, and manage Cresilon's Preclinical Research activities.

Requirements

  • A Bachelor's in a technical or scientific field is required.
  • Extensive knowledge of surgery, anatomy, toxicology, and pathology is required.
  • Strong communication skills (both written and verbal) is required with the ability to extract key facts from complex information and present concise summaries to management.
  • Demonstrated experience with large animal in vivo surgical research and CRO vendor management is required.

Nice to have

  • DVM, PhD or MD in a relevant discipline is preferred.
  • 4+ years of people management experience preferred.
  • Experience with surgical publication submission strategy is strongly preferred.

Compensation

  • $130k-$210k

Benefits

  • Plan, direct, coordinate, and execute activities related to the design, initiation. and follow-up of studies to support approval of Class I-III medical devices.
  • Ensure that the company operates within the scope of regulatory compliance, including Quality System Regulations (ISO 13485), health and safety, environmental protection regulations, and the core values of Cresilon.
  • Regularly interface with management to ensure research operations reflect overall corporate vision/strategy.
  • Work with the VP of Technology and the Director of R&D to ensure long-term vision and goals are met to reflect the company's charter.nd
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