About The Position

Lead prioritization of preclinical activities to ensure alignment with program timelines and organizational goals. Allocate resources, personnel, and equipment to meet study demands while maintaining flexibility for shifting priorities. Collaborate with scientists, engineers, and clinicians to design robust preclinical studies and experiments. Provide guidance on study methodology, model selection, sample size considerations, and data collection strategies. Ensure experimental plans meet scientific, regulatory, and ethical standards. Explore new model development Lead pre‑study planning activities including managing risk to the portfolio. Facilitate post-study debriefs to capture learnings, review data quality, and identify process improvements. Document outcomes and ensure knowledge transfer across teams. Serve as a primary point of contact for key stakeholders Build strong relationships with external partners, CROs, and academic collaborators as needed. Foster a culture of open communication, scientific rigor, and continuous improvement. Support onboarding, training, and development of team members. Stay up to date with the latest developments in laboratory techniques/technology and implement new methods and equipment to improve the efficiency and efficacy of research.

Requirements

  • Bachelor or Master's degree in biology, biomedical engineering, animal science, or related field; advanced degree preferred.
  • 5+ years of experience in preclinical research, medical device testing, or related laboratory environment.
  • Demonstrated experience coordinating complex studies or lab operations.
  • Strong organizational, communication, and problem‑solving skills.
  • Ability to work cross‑functionally and manage multiple priorities in a fast‑paced environment.

Nice To Haves

  • Leadership experience (formal or informal) strongly preferred.

Responsibilities

  • Lead prioritization of preclinical activities to ensure alignment with program timelines and organizational goals.
  • Allocate resources, personnel, and equipment to meet study demands while maintaining flexibility for shifting priorities.
  • Collaborate with scientists, engineers, and clinicians to design robust preclinical studies and experiments.
  • Provide guidance on study methodology, model selection, sample size considerations, and data collection strategies.
  • Ensure experimental plans meet scientific, regulatory, and ethical standards.
  • Explore new model development Lead pre‑study planning activities including managing risk to the portfolio.
  • Facilitate post-study debriefs to capture learnings, review data quality, and identify process improvements.
  • Document outcomes and ensure knowledge transfer across teams.
  • Serve as a primary point of contact for key stakeholders
  • Build strong relationships with external partners, CROs, and academic collaborators as needed.
  • Foster a culture of open communication, scientific rigor, and continuous improvement.
  • Support onboarding, training, and development of team members.
  • Stay up to date with the latest developments in laboratory techniques/technology and implement new methods and equipment to improve the efficiency and efficacy of research.
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