Scientific Associate Director - Safety Pharmacology

Amgen • Thousand Oaks, CA

6d

About The Position

Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Scientific Associate Director – Safety Pharmacology What you will do Let’s do this. Let’s change the world. The Scientific Associate Director will lead safety pharmacology lab-based activities within the Safety Pharmacology Sciences team and contribute directly to the success of Translational Safety & Risk Sciences (TSRS), the department responsible for nonclinical safety evaluation within Amgen Research. This role reports to the Senior Director of Safety Pharmacology Sciences. This leadership role has multiple components: management of in vitro cardiac safety and electrophysiology laboratory and staff; lead and coordinate safety issue resolution studies (in vitro; in vivo); serve as a Safety Pharmacology Subject Matter Expert (SME) on project teams; and contribute to external scientific initiatives. The role requires integration of data across multiple assay systems and modalities to support candidate selection, risk assessment, clinical translation, regulatory strategy, and advancement of industry best practices.

Requirements

• Doctorate degree [and relevant post-doc where applicable] and 4 years of relevant scientific experience OR Master’s degree and 7 years of relevant scientific experience OR Bachelor’s degree and 9 years of relevant scientific experience

Nice To Haves

• PhD in Pharmacology, Neuroscience, Physiology, Biomedical Sciences, or related field
• Broad experience in in vitro and or in vivo safety pharmacology across cardiovascular, respiratory and CNS domains
• Working knowledge of cardiac ion channel assays (e.g., hERG, Nav1.5, Cav1.2) and hiPSC-derived cardiomyocyte and isolated heart assays
• Experience managing outsourced studies and CRO relationships
• Experience supporting discovery and development project teams as a safety pharmacology SME or toxicology representative.
• Familiarity with GLP-enabling safety pharmacology packages and integration with toxicology studies
• Demonstrated people leadership and laboratory management experience
• Strong cross-functional communication and problem-solving skills
• Track record of scientific publications and participation in external scientific forums or consortia

Responsibilities

• Laboratory Leadership & Talant Management: Oversee the cardiac safety and electrophysiology laboratory, a core function responsible for ion channel, hiPSC-derived cardiomyocyte, and isolated heart assays. Manage exploratory and GLP-compliant studies, including outsourcing, protocol development, data review, and report finalization. Supervise scientific staff, promote their development and ensure high-quality timely data generation, study tracking, QC, reporting and stakeholder communication. Maintain compliance with data integrity, safety, and environmental standards. Interface with internal & external partners to establish qualified NAMs models for safety assessment.
• Safety Pharmacology Subject Matter Expert (SME) on TSRS Teams: Provide expertise to support discovery and development programs and partner with TSRS project team representative (PTR) and other team members (PKDM, pathology, etc) to ensure aligned and efficient execution of safety strategies. Ensure appropriate evaluation of target- and off target-based safety risks for diverse drug modalities in accordance with evolving ICH guidelines (S7A, S7B/E14, etc.). Guide study design, data interpretation, and next-step recommendations to support both lead optimization and clinical candidate selection and contribute to regulatory filings or inquiries. Provide oversight of safety pharmacology strategy across modalities, including small molecules, biologics, and emerging therapeutic approaches. Coordinate investigative studies (e.g. human primary tissue acquisition, functional studies, etc.) and partner with internal and external (CRO) labs to execute. Collaborate with relevant experts to evaluate and integrate in vitro and in silico approaches.
• External Scientific Influence: Build and maintain external collaborations with academic, industry, and consortium partners to advance mechanistic safety understanding and safety pharmacology best practices. Develop scientific eminence through peer-reviewed publications, presentations, and invited talks. Promote adoption of human-relevant in vitro models (e.g., stem cell–derived cardiomyocytes and other NAMs). Contribute to industry thinking on emerging modality-specific safety considerations (e.g., oligonucleotides and novel therapeutics).

Benefits

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible.

What This Job Offers

• Job Type: Full-time
• Career Level: Director