Quantitative Medicine Scientist-Statistics

This listing was posted on ApplicantPro.

Quantitative Medicine Scientist-Statistics

Location:

Tucson, AZ

Description:

Essential Job Duties and Responsibilities: Assist in planning modeling and simulation projects within existing Consortia, PPPs, and programs at C-Path Execute modeling/ statistical analysis plans. Accountable for implementation of modeling/ statistical analysis plans based on agreed upon best practices (i.e. model-based drug development). Works with multifunctional internal and external teams to deliver and report the assigned quantitative tasks. Responsible for use of quantitative methods to integrate disease-specific knowledge and clinical considerations for optimizing drug development. Responsible for appropriate summarization and interpretation of results of data analyses with respect to their impact on development of quantitative drug development tools. During the planning stages, works with internal and external teams to ensure that principles of model-based drug development have been applied. Prepare scientific summaries and reports which will be used for regulatory submissions and publications. Other duties and responsibilities may be assigned. Education and Training: PharmD, PhD, or equivalent training or experience in statistics, biostatistics, applied mathematics, pharmacometrics, systems pharmacology, engineering, engineering, pharmaceutical sciences or related discipline. Proficiency or experience working in team settings. Knowledge/Skill/Abilities: Quantitative methodologies: demonstrates thorough understanding of, or aptitude to learn, quantitative methods used in drug development: 1) statistical modeling , (mixed-effects models, survival models, Bayesian methods) Software: demonstrates thorough experience coding in formal and/or modeling software platforms . Communication: demonstrates ability to effectively present quantitative results, development plans, and strategies to technical and non-technical audiences in verbal form Writing: demonstrates ability to write clinical pharmacology results, interpretations (including impact) and conclusions for reports and regulatory documents that are clear and concise. Time Management: Ability to meet target deadlines and manage time effectively, balanced across multiple projects. Networking and Alliance Building: good interpersonal skills that ensure teamwork and productive interactions among diverse personalities/areas of expertise; ability to garner support and coordinate resources in support of consortia objectives. Innovation: constantly looking for new approaches and able to devise/apply new techniques in quantitative medicine, clinical pharmacology and modeling and simulation. Courage with Decisiveness to Act: bias towards action to achieve goals; excitement, enthusiasm and a sense of urgency with regard to the development of drug development tools. Values: Practice highest level of integrity and core value system consistent with C-Path's core values. Clinical Pharmacology: knowledge of principles of PK, PK-PD, phase I-III studies of drug development, biopharmaceutics, pathophysiology and therapeutics is desirable. Regulatory Knowledge : understanding of appropriate FDA, EMA and ICH guidelines in the design of analysis plans is desirable. Computer Skills: Proficient use of Microsoft Office Suite: Word, Excel, PowerPoint, Outlook. Proficient in programming in at least one of the following: R/STAN [preferred], Python, NONMEM Additional expertise with other quantitative tools (e.g., SIMCYP, GastroPlus, Matlab, Phoenix [Winnonlin, NLME], Stan, BUGS) or programming languages (e.g., C++, Java, Perl) a plus Physical Demands: Regularly required to sit for long periods of time, and occasionally stand and walk about the facility. Regularly uses hands to operate computer equipment and other office equipment. Close vision required for computer usage. Occasionally required to stoop, kneel, and lift up to 25 pounds. Travel on occasion for out-of-town meetings (~ 10%). In accordance with the Executive Order on Ensuring Adequate COVID Safety Protocols for Federal Contractors, C-Path has adopted a policy to comply with this requirement all C-Path employees must vaccinated to safeguard the health of our employees and their families; our customers and visitors; and the community at large from COVID-19. Reasonable Accommodation: Newly hired employees in need of an exemption from this policy due to a medical reason or because of a sincerely held religious belief must submit a completed request for accommodation form to the human resources department to begin the interactive accommodation process as soon as possible. Accommodations will be granted where they do not cause C-Path undue hardship or pose a direct threat to the health and safety of others. Please direct any questions regarding this policy to the human resources department. Job Posted by ApplicantPro

Company:

Critical Path Institute

Posted:

December 26 2023 on ApplicantPro

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Quantitative Medicine Scientist-Statistics | Scientist in Science & Pharmaceutical Job at Crit1

Quantitative Medicine Scientist-Statistics

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