Associate Medical Director / Medical Director

Arrowhead Pharmaceuticals•Pasadena, CA

9h•Onsite

About The Position

Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead’s RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead’s corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Associate Medical Director/Medical Director will report to the head of cardiometabolic clinical development and will be instrumental in bringing important new therapies based on RNA interference to patients. This individual will work collaboratively with Arrowhead’s scientific and clinical teams to take drugs from late clinical research to NDA filings and will initially focus on siRNA programs targeting cardiac and metabolic (lipids and obesity) indications. The Associate Medical Director will take hands on responsibility for designing and managing clinical studies to evaluate the efficacy, safety, dose selection and clinical pharmacology of product candidates. Candidates with the requisite experience may be considered for a Medical Director title. This is a fulltime, onsite position based from Arrowhead’s Corporate Headquarters in Pasadena, CA.

Requirements

M.D. or MD / Ph.D. combined with research experience
Hands-on translational research experience within a pharmaceutical or biotechnology company or in an academic setting
Demonstrated understanding of the drug development process and a strong desire to contribute to the development of meaningful therapeutics
Knowledge of Good Clinical Practices, FDA regulations and guidelines and applicable regulatory requirements
Ability to effectively evaluate outside expert advice
Ability to clearly elucidate complex scientific and medical concepts via written and oral communication
Working independently and effectively in a fast-paced, team-based environment
Strong clinical/scientific/technical skills
Strong interpersonal skills and the ability to communicate effectively with people in diverse and different settings
Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions
Project management skills and focus on delivery of results

Nice To Haves

Fellowship training (eg cardiology, endocrinology)
Research focused on lipids or obesity

Responsibilities

Support the conceptualization and design, development, execution and communication of clinical studies across a variety of therapeutic areas
Act as a medical lead in a cross functional team that includes medical, scientific, clinical, safety, program management and regulatory staff
Effectively communicate protocols and other relevant information with clinical site investigators and staff
Interpret clinical trial data and communicate results clearly and accurately
Provide ongoing clinical monitoring for clinical trials including but not limited to assessment of eligibility criteria, toxicity management, and drug safety surveillance
Contribute to documents, including IRB submissions, protocols, study reports, publications and regulatory submissions – including anticipated upcoming NDA/MAA submission
Provide high level and complex scientific and clinical guidance to Clinical Trials Management, Biometrics, Global Drug Safety, Regulatory and Project Management staff to meet project deliverables and timelines
Identify key opinion leaders and participate in clinical advisory board meetings
Make scientific presentations at advisory boards, key scientific meetings and external committee meetings
Identify and evaluate medical need and clinical path for new applications of RNA interference for the treatment of disease
Monitor and understand new developments in RNA interference in industry and academia
Support in-licensing and out-licensing activities and partner relationships