Senior Medical Director

2 weeks ago

Belmont CA, United States Mirum Pharmaceuticals Inc Full time

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases affecting children and adults. Using data and meaningful evidence, our goal is to transform scientific discoveries into therapies that are poised to positively impact the treatment of rare diseases. We are collaborative, creative, and experienced professionals and we're looking to augment our team with other individuals who embody our values: care, be real, get it done, and have fun, seriously. The Senior Medical Director will join the Clinical Development group and will be responsible for all clinical trial related activities in all stages of clinical development in a cross-functional team of internal and external experts, investigators and government agencies. Activities include but are not limited to protocol development, support study startup, oversight of trial execution, recruitment, ongoing clinical development management and closeout as appropriate. Compliance with internal processes, GCP/ICH and regulatory requirements, study and data monitoring, data analysis, are required. Participation in health authority meetings and regulatory filing activities are also part of this role. The Senior Medical Director operates in collaboration with other functions including internal Safety and Clinical Operations teams.
Leadership and management of all aspects of complex, global development clinical study program(s), from phase 1 through post-commercialization.
Primary point of contact for medical inquiries from sites, CRO and site monitors; answer or triage questions as appropriate integration of clinical/regulatory strategy into global product development strategy.
Primary liaison for internal Clinical Operations for site selection, site start-up activities, study management and closeout activities, etc.
Assist in authoring key clinical study documents, including Protocols, Clinical Study Reports, Investigator Brochures, Regulatory Authority briefing books, Development Safety Update Reports etc.
Responsible for medical monitoring of efficacy and safety clinical trial data.
Oversight of medical aspects of compliance of and inspection readiness in completed, ongoing and starting clinical trials.
Collaboration in the analysis and writing of scientific publications/presentations.
Works closely with other functions, in particular with Safety function and Clinical Operations.
Co-leads Study Management Team with Clinical Operations lead.
Knowledge and understanding of regulatory requirements for product approval and compliance in US and Europe.
Experience with basic statistical principles and techniques of data analysis, interpretation and clinical relevance.
Ability to understand and communicate risks, as well as develop and execute contingency plans.
Experience presenting data to regulatory agencies and advisory committees.
Knowledge of applicable regulatory.
Willingness and ability to travel domestically and internationally is required; Mirum Pharmaceuticals is committed to Equal Employment Opportunity (EEO) and to compliance with all Federal, State and Local laws that prohibit employment discrimination on the basis of race, age, national origin, ethnicity, religion, gender, gender identity, pregnancy, marital status, sexual orientation, citizenship, genetic disposition or characteristics, disability, veteran's status or any other classification protected by applicable State/Federal/Local laws.
Mirum Pharmaceuticals provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in job application procedures.
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