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SENIOR BIOSTATISTICIAN (FSP)

IQVIA • Remote • Posted 4 days ago

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Remote • Full-time • $122,800-$184,200/yr • Senior Level

Job Highlights

Using AI ⚡ to summarize the original job post

The Senior Biostatistician at IQVIA is responsible for providing statistical support for drug development programs across all phases of development. This role involves interacting with multidisciplinary project teams, providing statistical input to study protocols, writing statistical analysis plans, and contributing to regulatory documents such as clinical study reports. The position offers home-based remote working opportunities, a flexible schedule, and a variety of therapeutic areas to work in.

Responsibilities

  • Interact with members of the multidisciplinary project teams to establish project timelines.
  • Provide statistical input to study protocols.
  • Write the statistical sections of clinical trial protocols, consulting with internal and external experts.
  • Write statistical analysis plans.
  • Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.
  • Collaborate with Data Management, Clinical Development, and Clinical Operations on design of eCRFs.
  • Contribute to clinical study reports and other regulatory documents such as DSURs and Briefing Documents.
  • Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.
  • Interpret study results and review reports of study results for accuracy.
  • Participate and contribute to authoring of Clinical Development Plan.
  • Support exploratory analyses and medical affairs publications.
  • Participate in pre-IND and NDA activities.
  • Participate in the development and enforcement of SOPs and guidelines.
  • Participate in other activities and meetings to support Biostatistics and the Development Team as needed.
  • Consult with Research & Preclinical colleagues on statistical questions in their work.

Qualifications

Required

  • PhD in Statistics, Biostatistics, or related field with 5+ years industry experience
  • MS in Statistics, Biostatistics, or related field with 7+ years of industry experience
  • 1+ years with regulatory submissions
  • Successful publication experience
  • Ability to work independently in project management and decision making
  • Able to effectively communicate ideas and manage programmers in a constructive manner
  • Ability to use SAS and/or R to perform efficacy analyses and validate important data derivations when necessary
  • Experience with simulations

Preferred

  • Understanding of ICH GCP and general knowledge of industry practices and standards
  • Familiarity with R programming language and other statistical software, including EAST
  • Experience with Neuroscience therapeutic area and/or rare diseases
  • Experience with CDISC, including SDTM, ADaM, CDASH
  • Experience with Bayesian methods
  • Knowledge of simulations, multivariate analyses, and biomarker analyses

About IQVIA

IQVIA is a global company in the life sciences industry, offering advanced analytics, technology solutions, and clinical research services. They focus on driving healthcare forward by providing tailored solutions to various sectors such as pharmaceutical manufacturers, biopharma companies, and healthcare providers. IQVIA's key therapeutic areas include cardiovascular, oncology, and rare diseases, with a strong emphasis on leveraging cutting-edge technologies to deliver actionable insights.

Full Job Description

Job Level: Senior Biostatistician within DSSSLocation: Home-based in the U.S. or CanadaWhy DSSS?Data Sciences Staffing Solutions, DSSS or DS3, is a unit within IQVIA that provides our sponsors with fully embedded resources through a Functional Service Provider (FSP) partnership. This means you get all the benefits of working for an industry leading global CRO while operating within a sponsor environment and utilizing sponsor systems. These sponsor clients include world class pharmaceutical and biotech companies offering you unique opportunities to influence the future of medicine and advance therapies.Job Summary:The Senior Biostatistician is responsible for providing statistical support for drug development programs in all phases of development.Additional Benefits:Home-based remote working opportunitiesWork/life balance as well as flexible schedulesCollaborating with dedicated, high-performance, statistical and research teamsVariety of therapeutic areas, indications and, study phasesTechnical training and tailored development curriculumResearch opportunities that match your unique skillsetPromising career trajectoryJob stability: long-term engagements and re-deployment opportunitiesFocus on bringing new therapies to market rather than project budgets and change orders.Job Requirements:Interact with members of the multidisciplinary project teams to establish project timelines.Provide statistical input to study protocols.Writes the statistical sections of clinical trial protocols, while consulting with internal and external experts.Write statistical analysis plans.Monitor internal and CRO project activities including timelines, deliverables, and availability of resources.Collaborates with Data Management, Clinical Development, and Clinical Operations on design of eCRFs.Contributes to clinical study reports and other regulatory documents e.g., DSURs, Briefing Documents, etc.Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.Interpret study results and review reports of study results for accuracy.Participate and contribute to authoring of Clinical Development Plan.Support exploratory analyses and medical affairs publications.Participate in pre-IND and NDA activities.Participate in the development and enforcement of SOPs and guideline.Participates in other activities and meetings to support Biostatistics and the Development Team as needed.Consults with Research & Preclinical colleagues on statistical questions in their work.Qualifications (Minimal acceptable level of education, work experience, and competency)PhD in Statistics, Biostatistics, or related field with 5+ years industry experience.MS in Statistics, Biostatistics, or related field with 7+ years of industry experience.1+ years with regulatory submissionsSuccessful publication experience.Demonstrate ability to work independently in project management and decision making.Able to effectively communicate his/her ideas and to manage programmers in a constructive manner.Ability to use SAS and/or R to perform efficacy analyses and validate important data derivations when necessary.Experience with simulations.Desired Experience:Understanding of ICH GCP as well as general knowledge of industry practices and standards.Familiarity with R programming language and other statistical software, including EAST.Experience with Neuroscience therapeutic area and/or rare diseases.Experience with CDISC, including SDTM, ADaM, CDASH.Experience with Bayesian methodsKnowledge of simulations, multivariate analyses, and biomarker analyses#LI-Remote#LI-NITINMAHAJANIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.The potential base pay range for this role, when annualized, is $122,800.00 - $184,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.SummaryLocation: Durham, North Carolina, United States of AmericaType: Full time