Associate Scientific Director, Clinical Pharmacology

About this role

About This Role  

Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey.  

As the Lead, Clinical Pharmacology, Immunology, you will serve on program and study teams, providing strategic leadership in the development and execution of clinical pharmacology plans for drug candidates. You will integrate knowledge of clinical and quantitative pharmacology to optimize and provide rationale for dosage regimens ,   and study designs throughout the drug development lifecycle. This position is located in South San Francisco office or could be fully Remote . T he candidate must reside within the USA.  

What You'll Do  

• Provide clinical pharmacology expertise to program and study teams throughout a molecule’s lifecycle (discovery through development)  

• Provide functional representation on development program s and study teams and identify opportunities where modeling and simulation can ad vance the understanding of pharmacological activity, efficacy and safety   

• Develop & implement the clinical pharmacology development plan, considering all aspects (strategic, scientific, translational, and clinical)  

• Define key milestones and decisions within the clinical pharmacology development plan and identify risks and mitigation strategies  

• Lead execution of clinical pharmacology studies & analyses; interpret results and recommend action based on results  

• Conduct hands - o n quantitative ana lysis and present the findings to multidisciplinary project teams  

• Serve as lead author and key contributor to clinical pharmacology sections of documents  

• Serve as the subject matter expert in interactions with Health Authorities  

• Seek input from and ensure alignment with cross-functional partners, consultants, experts, and vendors as needed  

• Work with program and/or study teams to achieve program goals and provide deliverables in approved timeframes  

• Maintain cutting edge knowledge of best regulatory practices, quantitative/clinical pharmacology methodology , and drug development precedent  

Qualifications  

• PhD or MD/PhD in Pharmacology, Pharmacokinetics, Pharmaceutics or PharmD or other suitable related fields  

• 5+ years relevant industry experience (clinical pharmacology and/or clinical PK/PD)  

• Ability to analyze and interpret PK and PK/PD data utilizing sound scientific principles  

• Experience with designing and implementing relevant elements of clinical studies and/or dedicated Clinical Pharmacology studies  

• Ability to develop Clinical Pharmacology strategy in the context of the broader development paradigm  

• Knowledge of and ability to apply appropriate regulatory and ICH guidelines with regard to the acquisition, analysis, and interpretation of clinical pharmacology data  

• Hands - on experience with developing and implementing Quantitative Systems Pharmacology (QSP) models, and/or population PK, PKPD, exposure-response analyses  

• Experience with Model Informed Drug Development (MIDD) paired meeting program is a plus  

• Proficiency with use of PK/PD software packages such as Phoenix, R, NONMEM . E xperience with Monolix   and MATLAB is a plus  

• Excellent oral and written communication skills for effective interactions in various environments including, but not limited to, multidisciplinary teams, regulatory agencies, scientific symposia, and advisory boards  

#LI-TD1

Additional Information  

The base compensation range for this role is $144,000.00-$240,000.00. Base salary is determined by a combination of factors including, but not limited to, job-related years of relevant experience, internal equity, and location of the job. Additionally, this role is eligible for participation in Biogen’s LTI grants and other incentive programs. Biogen offers a full range of benefits that include medical, dental, life, long and short-term disability insurances, vacation, end-of-year shutdown, and 401K participation and matching contributions.  

Why Biogen?  

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.  

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.  

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.  

  Job Level: Management Additional Information

The base compensation range for this role is: $144,000.00-$240,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.

Regular employees are eligible to receive both short term and long-

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