Deciphera Waltham , MA 02154
Posted 2 weeks ago
Company Description
Deciphera is a biopharmaceutical company focused on discovering, developing and commercializing important new medicines to improve the lives of people with cancer. We are leveraging our proprietary switch-control kinase inhibitor platform and deep expertise in kinase biology to develop a broad portfolio of innovative medicines.
Enabled by our proprietary drug discovery platform, Deciphera has developed a diverse pipeline of wholly-owned drug candidates. QINLOCK (ripretinib) is Deciphera's switch control inhibitor developed for the treatment of fourth-line GIST. QINLOCK is approved in Australia, Canada, China, the European Union, Hong Kong, Switzerland, Taiwan, the United States, and the United Kingdom. We wholly own QINLOCK and all of our drug candidates with the exception of a development and commercialization out-license agreement for QINLOCK in Greater China. In addition to QINLOCK, we have identified and advanced multiple product candidates from our platform into clinical studies, including vimseltinib and DCC-3116.
See here for more details on our portfolio.
Job Description
We are seeking a Director of Biostatistics to join our team. In this role, the successful candidate will serve as the lead study statistician on one or more drug programs, which may include complex and/or pivotal studies. The successful candidate may also lead regulatory submission related tasks and represent Deciphera in communications with regulatory authorities.
This is an exciting opportunity to join a fast-paced oncology-focused biopharmaceutical company making a difference for patients globally. You will join a group of highly motivated, top-notch biostatistics and clinical development professionals and will be a key player in shaping the biostatistical strategy for key clinical studies. The role offers exciting opportunities for learning and growth as you partner cross-functionally to develop statistical analysis plans and contribute to the overall clinical development strategy.
This position will report to the Senior Director, Biostatistics and work on-site at our Waltham, MA office. Deciphera embraces a flexible workplace. You will work out of our Waltham, Massachusetts office. Deciphera expects a minimum number of in-office days. Specific days spent in the office should be determined in conjunction with your manager.
What You'll Do:
Serve as a lead statistician for one or more drug programs and manage statistical efforts for multiple clinical studies
Represent the biometrics functions on cross-functional and program teams and make strategic contributions to the clinical development plan (CDP)
Drives data-driven decision-making in a multidisciplinary team environment by providing a high level of statistical rigor to the analyses and interpretation of complex data generated.
Independently provides strategic and expert statistical input to drug development including feasibility assessments, development plans, complex study designs, and cross-study analyses including statistical methodology, interpretations, regulatory submissions, and follow-up.
Serve as the biostatistical lead in regulatory submissions and inspections
Contribute to clinical protocol development, including authoring of the section on statistical methods and reviewing/editing of other sections by applying statistical principles
Author/review statistical analysis plans for studies, ISS/ISEs, and author/edit shells for tables, figures, and listings
Review CRF designs to ensure data collection meet the study objectives and the requirements of statistical analyses
Provide statistical input to data monitoring committee (DMC) charters, project management plan, and other study-level documents
Work with statistical programmers or CROs to generate tables, figures, and listings
Perform ad hoc and exploratory statistical analyses as needed
Contribute to clinical study reports, including authoring of statistical sections and interpretation of the study results
Support the preparation of publications, including manuscripts, posters, and oral presentations
Provide oversight of CROs for outsourced statistical activities and QC key results generated by CROs
May manage FTE/contractor direct report(s) as needed
Qualifications
PhD in biostatistics, statistics, or a related field with at least 8 years of relevant clinical trial experience or MS in statistics or equivalent with at least 10 years of relevant clinical trial experience
Knowledge of statistical methods for clinical trials
In-depth Knowledge of FDA, EMA and ICH regulations and guidelines
Experience with NDAs/BLAs, MAAs and other regulatory submissions
Proficient in statistical programming (SAS or R is required)
Experience with trial design software (e.g., EAST or nQuery)
Good communication skills and ability to work with cross-functional study teams
Good influencing skills to ensure good statistical and quantitative expertise is adopted in clinical development
Good organizational skills, sufficient to multi-task in a fast-paced environment with changing priorities
Positive and collaborative attitude
Additional Information
We are proud to be Great Place to Work Certified 2023 and rank #25 on Fortune's Best Places to Work Small and Midsized Biotech Companies in 2023. Find more details about our award-winning culture here.
We offer an outstanding culture and opportunity for personal and professional growth based on our "PATHS" Core Values:
"How" we work together and the behaviors that we show up with each day are critical to maintaining our positive culture. Our behavioral expectations align with our values to elevate and drive individual and team performance:
Lead from where you are - regardless of role or level, we motivate each other to achieve common goals.
Drive business results - we navigate forward with our eye on the highest priorities.
Partner and collaborate - we cultivate relationships and value ideas, regardless of where they are coming from, to achieve more together.
Continuously evolve and improve - we try, we learn, we revise and try again.
Deciphera offers a comprehensive benefits package that includes but is not limited to the following:
Non-accrual paid time off
Summer vacation bonus
Global, company-wide summer and winter shutdowns
An annual lifestyle allowance
Monthly cell phone stipend
Internal rewards and recognition program
Medical, Dental, and Vision Insurance
401(k) retirement plan with company match
Life and Supplemental life insurance for family
Short and Long Term Disability insurance
ESPP offering
Health savings account with company contribution
Flexible spending account for either health care and/or dependent care.
Family planning benefit
Generous parental leave
[if applicable] Car allowance
Deciphera (NASDAQ: DCPH) is a publicly traded company headquartered in Waltham, Massachusetts. Our state-of-the-art research facility is located in Lawrence, Kansas and our European operations are run out of Switzerland.
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION
Deciphera is committed to equal employment opportunity and values diversity. To ensure that we comply with reporting requirements and to learn more about how we can increase diversity in our candidate pool, we invite you to voluntarily provide demographic information in a confidential survey at the end of this application. Providing this information is optional. It will not be accessible or used in the hiring process, and has no effect on your opportunity for employment. This information will also be treated confidentially. Our commitment to increasing diversity in our candidate pool does not affect our commitment to equal employment opportunity, including our ongoing commitment to make all hiring and other employment decisions solely on a nondiscriminatory basis.
Deciphera