Are you ready to join a team committed to making a meaningful impact on cancer treatment through the discovery and development of precision medicines? At Kura Oncology, you have an opportunity to be a part of something bigger, with a lasting impact that you can be proud of.
At Kura Oncology, we are working to change the paradigm and improve the science of cancer treatment. As an organization, we strive to cultivate a diverse and talented professional culture driven to develop precision medicine therapeutics.
As we continue to build a leading biotech organization with a strong culture, a patient-focused mindset and a team focused on relentless execution, we are looking for innovative, passionate professionals to join us and make our vision a reality.
To succeed at Kura, you will need to have a demonstrated ability for excellence in drug discovery and development and a roll-up your sleeves attitude. The ideal candidate will possess a values-driven work style where integrity and grit drive all behaviors, decisions, and actions.

JOB REQUIREMENTS

• Ph.D. in Pharmacokinetics, Pharmaceutical Sciences, or a closely related discipline with 5+ years of experience for Associate Director or 8+ years of experience for Director in clinical pharmacology, modeling & simulation, drug metabolism and/or pharmacokinetics within a large pharma and / or biotech companies
• Experience with nonclinical and clinical pharmacokinetic protocol design with experience working with CRO’s is required.
• Experience in Model Informed Drug Development.
• Strong organizational and time-management skills including the ability to manage several projects simultaneously.
• A strong entrepreneurial spirit and a desire to be hands on.
• Strong analytical and critical thinking skills, and attention to details.
• Demonstrated creativity in problem solving.
• Ability to effectively collaborate as part of cross-functional teams and with research partners.
• Excellent professional interpersonal skills, particularly oral and written communication skills and be able to work in a multidisciplinary team environment.
• Extensive knowledge of regulatory/guidance requirements (i.e. GLP, FDA, EMA) best practices pharmacokinetic/pharmacodynamic testing and risk assessment based on target indication.
  The base range for an Associate Director is $172,000- $203,000 and a Director is $228,405 - $260,000 per year. Individual pay may vary based on additional factors, including, and without limitation, job-related skills, experience, work location, and relevant education or training. Kura’s compensation package also includes generous benefits, equity, and participation in an annual target bonus.

• Provides clinical pharmacology leadership on multi-disciplinary teams for oncology programs including modeling & simulation to satisfy world-wide regulatory requirements.
• Provides clinical and nonclinical pharmacokinetic expertise to projects including study design, data analysis and interpretation.
• Develop population PK, exposure-response, mechanistic PK/PD, PBPK and QSP models, as needed, to evaluate risk/benefit and facilitate drug development decisions.
• Experience in developing clinical pharmacology and nonclinical strategy and execute studies such as but not limited to drug-drug interaction studies, specific population, BA/BE, and food effect.
• Provides clinical pharmacology support and leadership in preparation of various regulatory documents including study protocol, CSR, Investigator’s Brochure, Clinical Pharmacology section of INDs, CTAs, BLAs and/or NDAs, and clinical pharmacology section of package inserts.
• Participate in meetings with regulatory agencies and respond to regulatory queries