Senior Director - Clinical Pharmacology

February 25

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Logo of Spyre Therapeutics

Spyre Therapeutics

Spyre Therapeutics is a biopharmaceutical company focused on developing therapies for Inflammatory Bowel Disease (IBD). The company is committed to creating best-in-class antibodies, rational therapeutic combinations, and employing precision immunology approaches to enhance treatment efficacy and convenience for IBD patients. With a team experienced in developing and commercializing treatments across various diseases, Spyre Therapeutics is dedicated to improving treatment options and outcomes for patients through advanced research in immunology. The company fosters a collaborative and innovative environment to achieve its mission of providing promising new treatment options for IBD.

πŸ“‹ Description

β€’ Spyre Therapeutics is a biotechnology company that aims to create next-generation inflammatory bowel disease (IBD) and other immune-mediated disease products by combining best-in-class antibody engineering, rational therapeutic combinations, and precision medicine approaches. β€’ The Senior Director of Clinical Pharmacology will play a pivotal role in leading our clinical pharmacology efforts to advance the development of our cutting-edge antibody portfolio. β€’ This position requires a strategic leader who can integrate clinical pharmacology and pharmacokinetics/pharmacodynamics (PK/PD) strategies into our drug development programs to ensure efficacy, safety, and regulatory success.

🎯 Requirements

β€’ Ph.D. in Pharmacology, Pharmaceutical Sciences, or related field, with a strong focus on clinical pharmacology. β€’ A minimum of 10 years of experience in clinical pharmacology within the pharmaceutical or biotechnology industry, with significant experience in antibody development. Experience with extended half-life biologics and/or combination products desirable. β€’ Proven track record of accomplishment in drug development, from early-stage research through to regulatory submission and approval. β€’ Extensive experience with regulatory submissions and interactions with health authorities, particularly the FDA and EMA. β€’ Strong analytical and problem-solving skills, with expertise in PK/PD modeling and simulation. β€’ Excellent communication and interpersonal skills, with the ability to motivate teams and collaborate effectively across functions.

πŸ–οΈ Benefits

β€’ Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture of our young company, wear multiple hats, and learn quickly. β€’ Market-competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits. β€’ Unlimited PTO β€’ Two, one-week company-wide shutdowns each year. β€’ Commitment to growing you professionally and providing access to resources to further your development. β€’ 100% remote team with frequent in-person meetings to build relationships and problem solve.

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