Preclinical Study Coordinator

New

Skills

Cross-Functional Communication Data Recording GLP Compliance In Vivo Studies ISO 10993 Understanding MS Office Proficiency Project Management SOP Implementation Study Protocol Development Time Management

The Preclinical Study Coordinator will support the Study Director in the development of study protocols, amendments, and related documentation. This role is essential for facilitating cross-functional communication, tracking study timelines, and identifying roadblocks that may delay study progress.

Key Responsibilities
  • Assist in the development and management of study protocols and amendments.
  • Facilitate communication between cross-functional teams.
  • Track study timelines and milestones, ensuring timely completion of tasks.
  • Help identify and eliminate roadblocks to study progress.
  • Assist in the implementation of test methods and SOPs as outlined in the study protocol.
  • Ensure accurate recording and verification of experimental data.
  • Manage study schedules and alert the team to critical data collection points or deadlines.
Requirements & Qualifications
  • Bachelor's degree in biology, neuroscience, biomedical engineering, animal science, or a related field.
  • At least 1 year of experience in preclinical research support, study coordination, or project management.
  • Solid understanding of GLP (21 CFR Part 58) and ISO 10993; in vivo studies experience preferred.
  • Strong organizational and project management skills, capable of managing timelines and priorities effectively.
  • Attention to detail and proficiency in data compilation, documentation, and MS Office.
  • Experience working in animal research facilities with IACUC protocols.

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Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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