Senior Director, Clinical Development

Summary

Join Kura Oncology, a leading biotech company focused on precision medicine for cancer treatment, as a Senior Director, Clinical Development (MD). You will lead cross-functional teams in designing and conducting oncology studies, ensuring scientific rigor and collaboration across departments. This role requires a minimum of 3 years of relevant drug development experience and an MD or PhD. Success demands strong clinical research skills, excellent communication, and the ability to handle multiple projects. Kura offers a competitive compensation package, including a generous benefits package, equity, and a target bonus, along with career development opportunities and a supportive work environment.

Requirements

• Minimum of 3 years of relevant experience in drug development either in industry (preferred) or in academia
• M.D. or Ph.D. degree required
• Proven track record of strong clinical research skills, including publications
• Ability to partner with others to implement innovative development strategies
• Demonstrated excellence in independently leading and conducting research and ability to evaluate, interpret and present complex scientific data
• Demonstrated written and excellent communication and interpersonal skills, with the ability to translate statistical concepts into layman's terms
• Strong attention to detail with ability to understand the broader picture and priorities
• Must be a dedicated self-starter with a high energy level and ability to achieve results
• Must have strong communication and leadership skills-the ability to influence and work successfully with colleagues, customers, and corporate partners
• The candidate should have experience in handling multiple projects at a time

Responsibilities

• Lead cross-functional clinical teams for the design and conduct of oncology studies
• Ensure that scientific rigor and innovation drives Kura Oncology’s development strategies
• Ensure excellence in both strategy and execution by partnering closely with colleagues in clinical operations, biostatistics, data management, program management and translational medicine
• Serve as Medical Monitor of sponsored clinical research and as medical representative to CROs, reference laboratories and other organizations involved in the execution of clinical trials
• Responsible for of all clinical regulatory deliverables and other clinical documents associated with the clinical trials under his/her direct responsibility, including protocols, and the clinical portion of INDs, CTAs, investigator brochures, CRF’s, annual IND reports, CSR’s and clinical expert reports, among others
• Responsible for the analysis of clinical data, including safety monitoring in collaboration with PV
• Participate in site initiation visits and other site visits at clinical center

Preferred Qualifications

Experience in precision oncology/hematology preferred

Benefits

• Career advancement/ development opportunities
• 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!