Associate Director/Director, Clinical Scientist

Summary

Join Kura Oncology, a leading biotech company focused on precision medicine for cancer treatment, and contribute to our mission of improving patient outcomes. As an Associate or Director of Clinical Science, you will lead clinical study protocol development, collaborate with internal and external experts, and analyze study results. You will also support regulatory submissions and communicate study data to various audiences. This role requires an advanced clinical or science degree and significant experience in clinical study planning, execution, and reporting within the pharmaceutical industry. Kura offers a competitive compensation package, including generous benefits, equity, and bonus opportunities.

Requirements

• Candidates should have an advanced clinical or science degree (e.g. RN, MA, PharmD, NP, PhD)
• Must have a minimum of MA + 5 years of clinical or PharmD/PhD +3 years
• Technical/operational experience in planning, executing, reporting and publishing clinical studies within the pharmaceutical industry
• Demonstrated ability to review and summarize study data, including experience in preparing and presenting data
• Fluency in the English language, both written and verbal
• Thorough understanding of the drug development process from pre-IND through registration and post-registration required
• Broad understanding of functional areas of drug development, including preclinical, regulatory, pharmacovigilance, drug supply, data sciences (data management, biostatistics, programming), and clinical operations (including site selection, study start-up, study conduct, and finalization)
• Ability to understand, interpret and communicate clinical information including literature reviews, competitive intelligence, and changing treatment paradigms in order to apply knowledge to support a robust clinical development strategy
• Understanding of trial design and statistics in order to apply knowledge to the design of clinical protocols
• Successful track record for the ability to interpret, analyze, and present clinical data, including aggregate data analyses, in order to inform decision-making and set clinical strategy
• Hands-on experience performing systematic literature search, summarizing the search results and presenting the conclusions to wide spectrum of audience
• Ability to work effectively in a collaborative team environment where results are achieved through influence, cooperation, and the incorporation of multiple points of view
• Strong organization, documentation and communication skills with an ability to multitask
• Excellent interpersonal skills: ability to collaborate across disciplines
• Detailed knowledge of GCP, ICH Guidelines and current US FDA regulations
• Ability to travel up to approximately 30% of the time

Responsibilities

• Lead the clinical study protocol development process by translating the strategy and approved concept into executable, efficient clinical protocols and related documents
• In collaboration with internal/external experts on biostatistics, clinical pharmacology, translational medicine, clinical operations and data management, contributes to the development of the plan to execute on trial design including CRF design, data review plan, statistical analysis plan review and finalization
• Collaborate within Development on the review, analysis, and interpretation of study results and assures appropriate data review and accurate data reporting
• Identify study issues and program issues by reviewing and monitoring of emerging clinical data related to safety, efficacy and PK/PD. Develops sound, strategic solutions to issues and collaborates with the clinical study team to ensure issue resolution. Conduct literature reviews as needed for the interpretation of study data and development of next steps
• Works closely with the medical monitor to assure he/she is informed of pertinent study information, including but not limited to safety and efficacy data
• Support the development of program documents, including the clinical sections of various regulatory documents such as IND, clinical study reports, investigator brochures, annual reports and updates, and clinical sections of regulatory submissions to support product approvals
• Translational medicine: Support the implementation of target/pathway engagement assays for selecting therapeutically relevant doses and schedules; support stratification biomarkers
• In conjunction with the VP Development/CMO, develop presentations and communicate study data results to colleagues internally and to external audiences including investigators at sponsor meetings or general audiences at scientific conferences
• Maintain current knowledge of the external environment to ensure scientific innovations are considered and/or incorporated into clinical trial development strategy
• Serve as clinical science representative on cross-function teams as assigned

Benefits

• Competitive comp package
• Bonus
• 401K + Employer contributions
• Generous stock options
• ESPP Plan
• 20 days of PTO to start
• 18 Holidays (Including Summer & Winter Break)
• Generous Benefits Package with a variety of plans available with a substantial employer match
• Paid Paternity/Maternity Leave
• In-Office Catered lunches
• Home Office Setup
• Lifestyle Spending Stipend
• Commuter Stipend (Boston Office)
• Regular employee social activities, including happy hours, monthly birthday celebrations, Kura Koffee Talks, and much more!
• Career advancement/ development opportunities