Orna Therapeutics
Orna Therapeutics

51-200 employees

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Biotechnology
Pharmaceuticals
Healthcare
About Orna Therapeutics

Orna Therapeutics is a biotechnology company pioneering the development of circular RNA (circRNA) therapeutics. Their mission is to transform the treatment of diseases by leveraging the unique properties of circRNA to create more durable and effective medicines, including vaccines and protein replacement therapies. Founded in 2018, Orna Therapeutics focuses on innovative RNA engineering to address unmet medical needs in oncology, infectious diseases, and rare genetic disorders. The company combines cutting-edge science with scalable manufacturing to advance a new class of RNA medicines with the potential to improve patient outcomes globally.

5 months ago

PreClinical Safety Project Manager

Watertown - Office
Contract
Mid Level
Project Manager
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Description
  • Orna Therapeutics, a Watertown-based biotech startup focused on RNA therapeutics, is looking for a motivated and proactive PreClinical Safety Project Manager (CONTRACT).
  • The role involves managing operations within the Preclinical Safety Team, including study planning, scheduling, coordination with CROs, and ensuring regulatory compliance across Toxicology, DMPK, and Bioanalytical functions.
  • Responsibilities include overseeing study timelines, managing documentation, collaborating with internal and external teams, and maintaining organized records.
  • The ideal candidate will have a scientific background with experience in preclinical study management, regulatory guidelines, and project planning tools.
  • This position offers an opportunity to contribute to innovative therapies in a collaborative, fast-paced environment.

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Requirements
  • Master’s degree and 5+ years, or Bachelor’s degree and 10+ years, in a related scientific discipline such as Biochemistry, Pharmacology, Toxicology, or a related field
  • Experience in preclinical study management within the biopharmaceutical industry or at a CRO
  • Proficiency in managing preclinical studies and interfacing with CROs
  • Strong understanding of GLP regulations and other relevant regulatory guidelines
  • Experience with project planning tools such as Smartsheet or Project
  • Experience with data management systems and electronic data capture
  • Ability to anticipate challenges in study planning and develop rapid solutions
  • Excellent organizational and project management skills
  • Strong communication and interpersonal skills
  • Attention to detail and problem-solving capabilities
  • Ability to manage multiple projects simultaneously and adapt to changing priorities

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Benefits
  • This position will be eligible for benefits through Orna’s third party payroll provider
  • More information may be shared upon request during the interview process