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Interface with different teams, including in vivo scientists, QC/QA, Account Managers/Sales, and the veterinary staff. Are you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT.
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As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe. Associate Director, Toxicology - Cell & Gene Therapy. Experience with GLP (Good Laboratory Practice) and non-GLP toxicology studies.
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Knowledge and experience in cell and gene therapy programs are preferred. Ph. D. in Toxicology, Pharmacology, or a related field. Analyze and interpret study data, draw meaningful conclusions,make recommendations, and prepare comprehensive toxicology reports for clients and regulatory submissions.
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Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints. Your expertise will guide critical toxicology studies from conception to conclusion, ensuring excellence and integrity at every step.
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Act as the primary subject matter expert for clients, understanding their needs, providing advice, and addressing their toxicology-related inquiries and concerns. We are on the lookout for an exceptional individual to lead our client’s toxicology studies.
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LET ME WIN, BUT IF I CANNOT WIN, LET ME BE BRAVE IN THE ATTEMPT – Motto of the Special Olympics. THERE IS ONLY ONE WAY TO SUCCEED AT ANYTHING AND THAT IS TO GIVE EVERYTHING – Vince Lombardi. A minimum of 8 years of experience in toxicology, with a strong track record in designing and overseeing toxicology studies.
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If you're passionate about safeguarding product safety and thrive in providing expert guidance, this is your opportunity! Board certification in toxicology (e.g., DABT). Previous experience in a CRO or pharmaceutical/biotechnology industry.
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Associate Director, Toxicology - Cell & Gene TherapyAre you a seasoned Toxicologist ready to influence the future of Cell & Gene Therapy (CGT)? Your New Chapter Awaits:As a Senior Study Director in the CGT department, you’ll play a pivotal role in advancing the science that keeps us all safe.
$150,000 - $200,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Your Credentials: Ph. D. in Toxicology, Pharmacology, or a related field. Key Responsibilities: Lead the design and planning of toxicology studies, including selecting appropriate study models and endpoints.
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With a benefits package tailored to your life, you'll find everything you need to thrive both professionally and personally: Comprehensive health insurance with employer contributions. Access to an Employee Assistance Program for when life throws a curveball.
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Monitor study progress, ensuring adherence to protocols and regulatory standards. Develop study protocols, timelines, and budgets in collaboration with project teams. Our client doesn’t just offer jobs; they craft careers.
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Lead a team of research scientists, providing guidance and mentorship. Optional coverage for your family's life and AD&D.Complete employer-paid Short and Long-Term Disability. Flex Spending Accounts for health and dependent care.
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Support regulatory submissions and interactions as needed. Employer-funded Health Reimbursement Account. Full coverage for Employee Life and AD&D Insurance. Excellent written and oral communication skills.
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Leadership and team management experience. A k to secure your future, with a generous employer match.
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Work with cross segment teams to drive Marketing messaging, Sales Enablement campaigns, Product Development resources, Purchasing etc. Maintain Timely quoting (as needed) for Mars Veterinary Health hospitals.
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veterinary sales jobs in Carlsbad, CA
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