Position Summary:
We are seeking an experienced Associate Director to lead the pharmacokinetics and pharmacodynamics function (PKPD) at Atrium Therapeutics to advance research and development programs in genetic cardiomyopathy. This is a highly visible role within Research and Development within Development Sciences Department. The Associate Director will be accountable for PKPD strategy and execution across the research and development programs of antibody oligonucleotide conjugates, inclusive of bioanalytical sciences. The ideal candidate will apply strong scientific understanding of PKPD principles to biologic and/or oligonucleotide therapeutics to enable sound judgment to expeditiously advance the pipeline. We are seeking a strategic thinker with the desire to be a hands-on leader of a team of PKPD scientists. Title and compensation will be commensurate with experience
Job Responsibilities:
• Support all aspects of PKPD across programs from research into late-phase clinical development, including design, oversight, and interpretation of nonclinical and clinical PK, TK, and tissue distribution studies; apply PKPD principles to relate exposure to target engagement and PD biomarkers, inform dose selection, and support first-in-human dose rationale; assess immunogenicity impact on PK where relevant
• Set phase-appropriate bioanalytical strategy and oversee development of GLP-compliant PK and ADA assays in plasma and tissue matrices; oversee CRO management including RFP, SOWs, budget, timeline and sample logistics
• Represent PKPD on project and study teams; accountable for communicating PKPD strategy, data interpretation and supporting regulatory documents, including IND/CTA, briefing book, protocol, CSR.
• Manage, mentor, and develop a team of PhD and non-PhD scientists; set priorities, support career development, and build a collaborative, high-performing culture
Education and Experience Requirements:
• PhD in Pharmacokinetics, Pharmaceutical Sciences, Pharmacology, Analytical Chemistry, Biochemistry, or a related field
• 8+ years of biopharma/biotech experience in nonclinical and clinical PKPD and regulated bioanalysis, including a proven record of advancing programs from research into development; authoring/supporting IND submissions, and participating in regulatory interactions; oligonucleotide (siRNA, ASO) and/or large-molecule experience preferred
• Hands-on design and interpretation of nonclinical and clinical PK studies, including NCA ; strong understanding of PKPD principles
• Working knowledge of regulated bioanalysis (ICH M10, GLP/GCP) and experience overseeing PK and ADA assay development and sample analysis at CROs
• Prior experience managing and developing scientific staff at multiple levels, including PhD and non-PhD scientists; demonstrated ability to lead cross-functional initiatives and communicate complex data clearly to project teams and leadership
• Thrives in a small-company environment, comfortable with ambiguity, takes initiative, and a hands-on problem-solver
What We Provide:
• The base salary range for this role is $185,000-$205,000. The final compensation will be commensurate with such factors as relevant experience, skillset, internal equity and market factors.
• Atrium offers competitive compensation and benefits which include stock options & RSUs, as well as a 401(k) with an employer match. In addition, the comprehensive wellness program includes coverage for medical, dental, vision, LTD, and unlimited of time off including summer & winter breaks.
• A commitment to learning and development which includes a variety of programming internally developed by and for Atrium employees, opportunities for job-specific training offered by industry, and an education reimbursement program.
$185,000 - $205,000 a year
