Medical Director, Safety Science
Denali TherapeuticsAbout the role
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients.
We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients.
Denali Therapeutics is dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine.The Opportunity
In anticipation of the Company’s growth plans, Denali Therapeutics is looking for a Medical Director, Global Drug Safety. This role will work on assigned studies and/or programs therefore responsible for many aspects of safety activities including safety medical review, data analysis and interpretation, preparation of periodic regulatory safety submissions and study reports. He/she will also contribute to Inspection Readiness and continuous PV process improvement. The successful candidate will have experience in medical and scientific safety assessment in clinical development and preferably also working knowledge of NDA/BLA submissions and continued post-approval safety surveillance. He/she will be a proven collaborator and self-starter who has the ability to thrive in a matrixed environment. This individual must be able to work in a spirit of collaboration and service, while also operating with an appropriate level of independent judgment. Denali is seeking candidates with a can-do attitude who work with the highest integrity, fostering an environment of compliance and continuous improvement.
Responsibilities
Under supervision of the Executive Director, Safety Science and as per company policies and procedures, for assigned Denali programs, responsible for safety deliverables for assigned programs or studies.
Provides medical review of adverse event reports to ensure the accuracy, integrity and completeness of information entered in the safety database.
Provide safety content for study-level documents including protocols, ICFs, CSR, and when required, to IBs, INDs, CTAs, and NDA/BLA/MAAs
Coordinating the program level Safety Management Team (SMT) to review safety signal evaluation reports and recommendations for risk characterization.
Responsible for the completion of safety regulatory submissions such as development safety update report (DSUR) and other aggregate safety reports for regulatory agencies worldwide
Track implementation of SMT and DSC decisions.
May support responses to questions from regulatory authorities.
Support regulatory agency audits and inspections, and corrective action plans.
Support PV vendor oversight in collaboration with Safety Operations
Lead direct report(s) through annual goal setting, growth planning, adherence to company policies, maintain training compliance and provide ongoing feedback on growth, development and areas of improvement.
Qualifications:
Advanced medical degree (e.g., MD, MBBS, DO) required
10+ years of experience in the drug safety and pharmacovigilance with a track record of successful deliveries of core safety/PV activities in cross-functional safety teams.
8+ years of management responsibility
Strong working knowledge of global PV requirements (e.g., US Code of Federal (CFR) regulations; European Union (EU); Guideline on Good Pharmacovigilance Practices (GVP) and ICH Guidelines.
Strong interpersonal skills that facilitate collaboration across functions to reach consensus on safety topics.
Willingness to teach and to learn.
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