Associate Director Quantitative Science

Profile

Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were founded to make a big difference in small patient populations. Now we seek to make an even greater impact by applying the same science-driven, patient-forward approach that propelled our last 25 years of drug development to larger genetic disorders, as well as genetic subsets of more common conditions. Through our unparalleled expertise in genetics and molecular biology, we will continue to develop targeted therapies that address the root cause of the conditions we seek to treat. Applying our knowledge to make a transformative impact is not just a calling, but an obligation to those who will benefit most. The end goal has always been better lives and now we can reach more. And the more people we reach, the more our impact can grow. We transform lives through genetic discovery. Our Culture Our desire to make a positive impact on our patients extends to our employees and BioMarin is committed to fostering an inclusive environment where every person feels seen, valued, and heard u2013 so employees can thrive in all areas of their lives, in and outside of work. We seek to provide an open, flexible, and friendly work environment to empower people and to provide them with the ability to develop their long-term careers. Ultimately, we want to be an organization where people enjoy coming to work and take pride in our efforts to help patients. *Note* Job can be hybrid, remote, or onsite in either San Rafael or Brisbane locationsSummaryThe Associate Director Quantitative Science (Post-Approval) is a self-sufficient and high-impact position focusing on supporting the statistical needs in the post-approval area in terms of rapid response for critical requests, exceptional communication and collaboration abilities, a broad practical perspective on contributing to the success of medical affairs and market access efforts, and technical leadership in formulating, interpreting, and communicating statistical approaches. Specifically, the applicant must have demonstrated the following qualifications. Subject matter expert in related technical areas such as real-world data/evidence (RWD/E), patient centric outcomes (PCOs), health economics and outcomes research (HEOR), and contemporary statistical modeling techniques (e.g., prognostic / predictive modelling, indirect treatment comparison, Bayesian analysis, etc.). Proficient data science analytical and programming skills. Excellent matrix team leadership and interpersonal skills.The positionu2019s primary responsibilities will include the following Leading a Data Science project team.u00A0 Directing / supporting all statistical activities from design to ad-hoc analysis to reporting and presentation.u00A0 Performing all tasks from statistical thinking to programming.u00A0u00A0Responsibilities Functions as a statistical / analytical subject-matter expert in all post-approval areas, especially Medical and Market Access / HEOR.u00A0 Ensures creative and effective statistical methodologies are identified and implemented in designs, analysis plans, and reporting and interpretation of post-approval study outcomes and statistical analyses.u00A0 Provides operational statistical leadership for the post-approval study teamu2019s and Market Access teamu2019s statistical needs in HEOR, health technology assessments (HTAs), price negotiation and reimbursement dossiers, observational research, and other medical and scientific communication activities.u00A0 Collaborates effectively with internal stakeholders from Clinical Development, Medical Affairs, HEOR, and RWE teams and external stakeholders (e.g., regulators, payers, review boards, co-authors, CROs, etc.).u00A0 Works proactively and efficiently with the Quantitative Science leads, Clinical Development statistical leads, and other colleagues within Data Science to organize, plan, manage, and control deliverables against goals and timelines.u00A0 u00A0 Serves as the lead for the Data Analysis Working Group (DAWG), Data Analysis and Reporting Team or Statistical Analysis Review Team (DART) for a therapeutic area (TA) or a program. u00A0 Contributes to clinical study reports (CSRs) and related periodic reports, and to authoring or co-authoring methodological or study-related presentations, posters, and manuscripts.u00A0 Understands modern drug discovery, research, development, and post-approval principles and processes.u00A0u00A0Education & ExperienceM.S. in Biostatistics, Statistics, Data Science, Pharmacoeconomics, or similar field required.u00A0Ph.D. in Biostatistics, Statistics, Data Science, Pharmacoeconomics, or similar field preferred.Minimum QualificationsA minimum of 5 (PhD) u2013 7 (Masteru2019s) yearsu2019 experience in pharmaceutical and/or biotech industry. at least 3 (PhD) - 4 (Masteru2019s) years of working experience in post-approval, RWE, or market access/HEOR areas.u00A0Preferred Qualificationsu00A0Overall Must be able to effectively collaborate with cross-functional teams in the realization of clinical programs and initiatives from study design to presentation of results.u00A0 In-depth knowledge of Market Access / HEOR statistical needs and statistical methodology, as well as hands-on data analysis experience.u00A0 Must be able to provide technical and tactical support for cross-functional Medical Affairs and Market Access / HEOR programs including registries, burden of Illness / natural history of disease for regulators, payers, and clinicians.u00A0 Must be able to work effectively in a constantly changing, diverse, and matrix environment.u00A0Statistics Advanced knowledge of theoretical and applied statistics or other related data sciences. u00A0 In-depth knowledge of statistical analysis methods, especially on data originated from post-approval areas, especially Medical Affairs and Market Access / HEOR.u00A0 Solid programming skills including SAS, R, Python and other statistical software packages.u00A0Supervisory Ability to lead, motivate, and mentoru00A0internal and contract staff.u00A0 Must be able to effectively review documents drafted by staff. u00A0Regulatory Must be knowledgeable of FDA, EMA and ICH regulations and guidelines.u00A0 Must be knowledgeable about HEOR / HTA requirements and guidelines. PLEASE NOTE: Absent a Medical or Religious reason that prohibits vaccinations, all our incoming employees must be vaccinated for COVID-19. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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