Associate Director, Project and Regulatory Toxicologist

Vividion Therapeutics, Inc•San Diego, CA

9h•$190,000 - $220,000•Onsite

About The Position

Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space. We are uniquely structured with opportunities for all scientists to contribute to both established programs as well as ongoing early target selection, screens and validation. We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression. Vividion was top ranked mid-size company on The San Diego Union-Tribune's 2022 to 2025 Top Workplaces list. The Project and Regulatory Toxicologist will be expected to use his/her toxicology expertise to guide safety assessment, design and interpret in vitro/in vivo studies to evaluate the safety profiles of our covalently and non-covalently targeted small molecules according to regulatory guidelines. You will work closely with the toxicology function, CROs, and multidisciplinary drug discovery/development teams to progress promising therapeutics to the clinic.

Requirements

Ph.D. in pharmacology, toxicology, or closely related biomedical disciplines with 6+ years of industry experience or M.S in above field with 10+ years of industry experience
Diplomate of American Board of Toxicology is highly desired
A broad understanding of various aspects of nonclinical safety assessment and regulatory requirements for drug development, experience representing toxicology function on discovery and development teams is required, expertise in immunology is highly desired
Must be able to critically evaluate, interpret and integrate multidisciplinary data to support target and compound safety assessment and mechanistic derisking
Experience in the design, conduct, and data interpretation of in vitro and in vivo safety pharmacology, genetic toxicology, and general toxicology studies are required
Experiences working with CROs
Excellent interpersonal skills, with the ability to interact professionally and effectively in a dynamic, multi-disciplinary, and highly collaborative team environment
Excellent verbal and written communication skills
Solid problem-solving skills with a strong sense of urgency and scientific curiosity
Proactive and agile, with the ability to operate in a fast-paced work setting
Solution and result-oriented with attention to details

Nice To Haves

Diplomate of American Board of Toxicology is highly desired
expertise in immunology is highly desired

Responsibilities

Represent toxicology function as a subject matter expert on drug discovery and development project teams and provide guidance on the safety characterization, prioritization and advancement of drug candidates
Directly interface with CROs to place appropriate in vitro and in vivo toxicology studies in a timely manner; manage and oversee the execution of toxicology studies at CROs to ensure high quality data delivery; review and QC study protocols, results, and study reports; summarize toxicology study results and communicate toxicology findings to project teams and senior management accurately and punctually
Contribute to the writing of safety study summary, nonclinical overview and other regulatory documents, represent Vividion at regulatory interactions
May need to identify and implement new strategies on safety assessment to address current and future safety-related challenges, keep abreast of current regulatory requirements by participating in cross-industry consortium or scientific conferences
Collaborate with early discovery project teams to conduct literature-based target safety assessments and provide guidance on target safety derisking activities