Executive Director, Clinical Development
Kura Oncology - Boston, MA
posted 4 days ago
About the position
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.
Responsibilities
- Lead cross-functional clinical teams for the design and conduct of oncology studies, specifically with the FTI franchise.
- 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 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.
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.
- Experience in precision oncology/hematology preferred.
- 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.
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!
