Senior Biostatistician FSP, Late Phase
Durham, North Carolina, United States of America
Job Level: FSP Senior Biostatistician for Phase 2/3
Location: Home-based in the U.S. or Canada
Why DSSS?
Data Sciences Staffing Solutions, 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 collaborating with sponsor teams 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 to market.
Job Summary:
The Senior Biostatistician is responsible for providing statistical support for drug development programs in phases 2 or 3 with efficacy and safety endpoints.
Additional Benefits:
- Home-based remote working opportunities
- Work/life balance as well as flexible schedules.
- Collaborating with motivated, high-performance, statistical and research teams
- Technical training and tailored development curriculum
- Research opportunities that match your unique skillset
- Promising career trajectory
- Job stability: long-term engagements and re-deployment opportunities
- Focus on bringing new therapies to market rather than project budgets and change orders.
- Experience with regulatory submissions.
- Engaging, fast-paced environment
- Good work-life balance
Job Responsibilities:
- Collaborate with multidisciplinary project teams to establish project timelines.
- Provide statistical input to study synopses and protocols.
- Writes or reviews the statistical sections of clinical trial protocols, while consulting with internal and external experts.
- Write or review statistical analysis plans, dataset and TLF specifications.
- Provide guidance and supervision to programmers in authoring of analysis dataset specifications and programming of tables, listings, and figures.
- Effectively manage internal and CRO project activities including timelines, deliverables, and availability of resources.
- Collaborates with Data Management, Statistical Programming and Clinical Development, with statistical expertise.
- Use SAS and/or R to perform inferential analyses and validate important data derivations.
- Support exploratory analyses and publications.
- Contributes to clinical study reports and other regulatory documents e.g., DSURs, Briefing Documents, Benefit-Risk analyses, IB, etc.
- Participate in NDA and related activities.
- Participates in activities and meetings to support Biostatistics and the Development Team.
- Demonstrated ability in working independently, project management and decision making.
- Able to effectively communicate statistical concepts.
- Compliance with SOPs and best practices to ensure quality work product.
Qualifications (Minimal acceptable level of education, work experience, and competency)
- PhD in Statistics, Biostatistics, or related field with 3+ years industry experience.
- MS in Statistics, Biostatistics, or related field with 5+ years of industry experience.
- Understanding of ICH and FDA Guidance as well as general knowledge of industry practices and standards.
- Experience with CDISC, including SDTM, ADaM, CDASH.
Desired Experience:
- Familiarity with R programming language and other statistical software, including EAST.
- Knowledge of simulations, multivariate analyses, and biomarker analyses
- Experience in a range of therapeutic areas
- Production programming of statistical outputs
- Regulatory submission activities
- Estimand framework
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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
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. https://jobs.iqvia.com/covid-19-vaccine-status
The potential base pay range for this role, when annualized, is $115,900.00 - $193,100.00. 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. ApplyJob Profile
Benefits Bonuses Career development Career trajectory Compensation Equal employment opportunities Flexible schedules Healthcare Incentive plans Job stability Medical Remote work Technical training Work-life balance
Tasks- Collaborate with project teams
- Communicate statistical concepts
- Manage project activities
- Provide statistical support
- Support exploratory analyses
- Write/review statistical sections
ADaM Biomarker analyses Biostatistics BioTech CDASH CDISC Clinical Development Clinical Research Clinical trial protocols Clinical trials Compliance Consulting Data Management Decision making Drug Development Education Exploratory analyses FDA Healthcare ICH Inferential analyses Management Multivariate analyses Programming Project Management R Regulatory Submissions Research SAS SDTM Simulations Statistical analysis Statistical analysis plans Statistical Programming Supervision Training
Experience3 - 5 years
EducationHealthcare Life Sciences MS Ph.D. Project Management Related Field Statistics
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9