<p>Position: Senior Scientist, CGT Preclinical</p> <p>Salary Range: $120k - $125k</p> <p>Location: Carlsbad, CA (on-site)</p> <p>About Pharmaron</p> <p>Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.</p> <p>We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit www.pharmaron.com.</p> <p>Job Overview:</p> <p>Pharmaron is seeking a Senior Scientist - CGT Preclinical to support the design, execution, and interpretation of in vivo studies for cell and gene therapy programs.</p> <p>This role will serve as a Study Director and scientific lead, focusing on toxicology, pharmacology, and biodistribution studies across therapeutic areas including CNS and oncology. The successful candidate will collaborate with internal teams and external sponsors to ensure studies are scientifically robust, operationally efficient, and compliant with regulatory standards.</p> <p>This position offers the opportunity to contribute to innovative preclinical research in a fast-paced CRO environment while supporting the development of advanced therapies.</p> <p>Key Responsibilities</p> <ul> <li>Serve as Study Director, leading the design, execution, analysis, and reporting of in vivo preclinical studies </li><li>Drive scientific strategy across toxicology, pharmacology, and biodistribution programs </li><li>Partner with sponsors to develop scientifically robust and cost-effective study designs </li><li>Collaborate with in vivo operations, veterinary staff, and QA/QC teams to ensure efficient study execution </li><li>Prepare and review GLP-compliant study protocols, IACUC documentation, and final reports </li><li>Provide subject matter expertise in CNS and oncology models, including immunocompromised systems </li><li>Perform and guide complex in vivo procedures, including stereotaxic injections and advanced dosing techniques </li><li>Ensure compliance with regulatory standards (USDA, FDA, AAALAC, OSHA) </li><li>Maintain accurate study records and contribute to internal database systems </li></ul> <p>What We're Looking For:</p> <ul> <li>D. in Pharmacology, Toxicology, Immunology, or related scientific discipline </li><li>3+ years of industry experience in preclinical in vivo research (CRO experience preferred) </li><li>Demonstrated experience as a Study Director or scientific lead </li><li>Strong technical expertise in: </li><li>CNS and/or oncology in vivo models </li><li>Surgical procedures (e.g., stereotaxic injections) </li><li>CGT-related preclinical systems </li><li>Experience preparing GLP-compliant protocols, reports, and regulatory documentation </li><li>Knowledge of regulatory standards (FDA, USDA, AAALAC) </li><li>Excellent communication skills with experience interacting with external sponsors </li><li>Ability to thrive in a fast-paced, matrixed environment </li></ul> <p>Why Pharmaron?</p> <p>Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.</p> <p>Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.</p> <p>Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:</p> <ul> <li>Insurance including Medical, Dental & Vision with significant employer contributions </li><li>Employer-funded Health Reimbursement Account </li><li>Healthcare & Dependent Care Flexible Spending Accounts </li><li>100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance </li><li>401k plan with generous employer match </li><li>Access to an Employee Assistance Program </li></ul> <p>How to Apply:</p> <p>Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!</p> <p>As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.</p> <p>#LI-MC1</p>