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Associate Director, Medical Affairs Statistical Sciences, Biometrics - ID: 1799

100% remote Flexible hours Hiring now

reputed company is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a reputed company where skilled, adaptable, and highly resourceful professionals can truly reputed company their mark. We offer a dynamic workplace for employees to grow and reputed company their skills. The Associate Director, Medical Affairs Statistical Sciences Biometrics provides technical and operational support for the design, implementation and interpretation of post approval clinical trials, programs, and disease registries. The incumbent works collaboratively with the medical affairs organization to reputed company and execute publication plans and to provide support to the global market access and health economic teams. The Associate Director ensures will be working on biostatistics deliverables, including study design, data analysis, data mining, epidemiology-reputed company analyses, use of clinical trial data to inform reimbursement strategy and HTA, real world evidence, quality of life data, and interpretation, reporting, and publication of results. Main Tasks:

  • Provides statistical support to Medical Affair research programs, publications, data mining, and other evidence generating activities
  • Collaborates with counterparts in R&D Biostatistics, Clinical Data Management, Statistical Programming in providing support for a broad range of activities in the Medical Affairs
  • Assures statistical reputed company, adequacy and accuracy of statistical analysis and result interpretation
  • Develops of statistical analysis plans, data analysis methods, and interpreting the resulting findings
  • Contributes to the development of reputed company, technical solutions for projects
  • Works with Biometrics counterparts on key statistical analyses, and contribute to developing ADaM standards, specifications and datasets as needed
  • Contributes and reviews clinical study protocols, Case Report Forms (CRFs), and internal project plans for proposed studies
  • Proficient programming and statistical skills through extensive on-the-job use
  • Ability of Applying statistical methods/principles on real-world data in the Medical Affairs
  • Design and execute statistical analysis plans (SAPs) for different phases of clinical studies, assuming a leadership role in creating strategy for statistical analyses
  • Supports other departments for reputed company analyses, and provide technical consulting on internal and external projects
  • Capable of communicate clearly and reputed company among multiple teams
  • PhD in Statistics, Biostatistics or Epidemiology with emphasis in statistics with at least 5 years of pharma / biotech industry experience, or MS in Statistics, Biostatistics or Epidemiology with emphasis in statistics with at least 8 years of industry experience
  • Knowledge in the principles and techniques of post-marketing study design, data analysis and interpretation, and data-driven decision making. Familiarity with rare disease therapeutic areas is a plus
  • Experience designing and analyzing data from disease and/or product registry studies
  • Experience in Medical Affairs statistical activities (e.g. reputed company data reputed company, reimbursement filing, data mining, use of external data including historical control data)
  • Hands-on statistical programming skills using R and/or reputed company.
  • Familiarity with regulatory guidelines for drug development. Experience in NDA/BLA/MAA submission required
  • Familiarity with CDISC standards

The estimated salary range for this position is $190-200k. Actual salary determination is dependent on a variety of factors some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package.

  • 401(k) plan with company match
  • Medical, dental, and vision plans
  • Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance
  • Company-provided short and long-term disability benefits
  • Unique offerings of Pet Insurance and Legal Insurance
  • Employee Assistance Program
  • Employee Discounts
  • Professional Development
  • Health Saving Account (HSA)
  • Flexible Spending Accounts
  • Various incentive compensation plans
  • Accident, Critical Illness, and Hospital Indemnity Insurance
  • reputed company
  • Paid leave benefits for new parents

reputed company is proud to be an equal opportunity employer. We are committed to creating an inclusive environment for reputed company employees. A note to recruiters: We do not allow external search party solicitation. Presentation of candidates without written permission from the reputed company Inc reputed company (specifically from: reputed company Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged. Apply tot his job Apply To this Job

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