Scientist

About the role

Frontage Laboratories Inc. is seeking a detail-oriented and highly collaborative Scientist to act as a Study Director for in vivo toxicity and PK/TK studies. The successful candidate will direct these studies to ensure project timelines are met, and effectively communicate with project managers, clients, and internal teams.

Responsibilities

• Study direction of in vivo non-GLP and GLP general toxicology and PK/TK studies.
• Initiate, monitor and oversee studies
• Interpret experimental data
• Author study protocols and reports.
• Acts as a primary point of study contact
• Maintain schedule of projects and timelines to meet client program milestones
• Maintain the proper level of regulatory compliance for each study and addressing QA audit findings
• Maintain and facilitate communication with sponsors and management
• Help with training and/or mentoring of junior scientific staff.
• Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties.
• Work with support teams including sample management, vivarium, QC, RW, PM & QA, BD as well as PIs and management.
• Other duties as assigned.

Qualifications

• B.S. in Toxicology, Pharmacology or related scientific discipline with a minimum of 2 years of CRO or pharmaceutical experience.
• Excellent communication, interpersonal, and technical writing skills.
• Understanding of common in vivo toxicological study endpoints
• Ability to organize and clearly present complex data and concepts
• Ability to work on multiple projects at the same time
• Understanding of GLP requirements
• Ability to successfully independently and corroboratively in a team environment

Benefits

Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc.