About the Role:The Senior Scientist, Bioanalysis & PK Operations will support the planning, coordination, and execution of non-regulated bioanalytical, PK, and TK activities. The role will manage BA/PK/TK study outsourcing, CRO and vendor relationships, critical reagent outsourcing, sample and shipping logistics, contracting and invoicing, study tracking and documentation, and cross-functional operational workflows. The position will partner closely with Bioanalysis, PK, in vivo, and project teams to ensure efficient study execution and timely delivery of high-quality data.
Your Contributions (include, but are not limited to):- Coordinate non-regulated Bioanalysis and PK operations from study request through completion, including study tracking, documentation, and data management workflows
- Coordinate and manage outsourcing of BA, PK, and TK studies, including CRO selection/engagement, study setup, monitoring, timelines, deliverables, and issue resolution
- Manage outsourcing and logistics for critical reagent development and production, including vendor coordination, shipping, tracking, and inventory
- Support PK study design, planning, execution, and monitoring in collaboration with PK, BA, in vivo, and project teams
- Manage domestic and international sample and reagent shipments, including applicable shipping requirements and documentation
- Support CRO/vendor management, contracting, purchase orders, invoicing, and study/reagent logistics for non-regulated activities
- Coordinate sample and study data management, from physical sample assets through digital databases, study documentation, and data delivery
- Serve as an operational representative on discovery and development project teams, supporting study readiness, cross-functional alignment, and timely execution
- Contribute to the preparation and review of study reports and IND/CTA-enabling documentation, as appropriate
Requirements:- PhD in pharmaceutical sciences, pharmacokinetics, bioanalysis, analytical chemistry, biology, or related discipline with 2+ years of relevant experience; OR
- MS with 4+ years; OR
- BS with 6+ years of relevant industry experience
- Experience supporting nonclinical PK, pharmacology, toxicology and/or bioanalytical studies in a pharmaceutical/biotechnology or CRO environment
- Experience with CRO/vendor management and outsourcing, including study coordination, timelines, deliverables, contracting, and invoicing
- Working knowledge of bioanalysis and PK study workflows, including sample management, study documentation, and data/reporting processes
- Experience coordinating biological sample and/or critical reagent shipments, including domestic and international logistics
- Strong project management, organizational, communication, and cross-functional collaboration skills with the ability to manage multiple studies and priorities
- Experience with electronic study/data management systems such as Benchling, Smartsheet, SharePoint, or similar platforms preferred
- Experience with critical reagent outsourcing/management and IND/CTA-enabling activities is a plus
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The annual base salary we reasonably expect to pay is $130,800.00-$179,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
