HireFT
Browse JobsHow it worksPricingAboutSuccess Stories
    Back to jobs
    FR

    Frontage Laboratories

    Contract Research Organization (CRO)

    Scientist

    Concord, United StatesOn-SiteFull-time2+ yrs experiencePosted 9h ago
    All Frontage Laboratories jobs

    Job description

    Title: Scientist

    Location: Concord, OH 

    Reports To: Manager, Safety and Toxicology

    Company

     Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

     Position Summary:

     We are 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.

    Education and Requirements:

    • 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

    Salary and 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.

    Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

    Job details are sourced from the employer's original posting.

    Open job posting
    FR

    About the company

    Frontage Laboratories

    Frontage Laboratories is a contract research organization (CRO) that provides comprehensive drug discovery, development, and manufacturing services to the pharmaceutical and biotechnology industries.

    View all Frontage Laboratories jobs
    Industry
    Contract Research Organization (CRO)
    Open roles
    98

    Interested in this role?

    Apply with HireFT

    Free to start — no card required.

    Your fit

    How well do you match?

    Sign in to see how your résumé lines up with this role.