Principal Biostatistician FSP, Cardiovascular
Bloomington, Illinois, United States of America
Job Level: FSP Principal Biostatistician (FSP) for Early Phase Cardiovascular/Cardiac Research
Location: Home-based in the U.S. or Canada
Why 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 collaborating directly with cross-functional sponsor teams. 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 Principal Biostatistician is responsible for providing statistical support for early phase drug development studies in cardiovascular/metabolism patients.
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 Requirements:
- Collaborate with multi-disciplinary project teams to establish project objectives and timelines.
- 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 with statistical expertise.
- 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.
- Support exploratory analyses and medical affairs publications.
- Participate in pre-IND and NDA activities.
- Participates in other activities and meetings to support Biostatistics and the Development Team as needed.
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.
- At least 4 years in early phase experience and cardiac/cardiovascular/metabolism studies in patients.
- 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.
- Understanding of ICH GCP, ICH E9 plus general knowledge of industry practices and standards.
- Experience with CDISC, including SDTM, Adam, CDASH
- 1+ years with regulatory submissions
- Successful publication experience.
Desired Experience:
- Familiarity with R programming language and other statistical software.
- Knowledge of simulations, multivariate analyses, and biomarker analyses
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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 $131,300.00 - $243,900.00. 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 teams
- Interpret study results
- Monitor project activities
- Provide statistical support
- Support exploratory analyses
- Write statistical sections of protocols
ADaM Biomarker analyses Biostatistics CDASH CDISC Clinical Development Clinical operations Clinical Research Clinical trial protocols Consulting Data Management Decision making Drug Development Education Exploratory analyses GCP Healthcare ICH ICH GCP Management Multivariate analyses Programming Project Management R Regulatory Submissions Research SAS SDTM Statistical analysis Statistical analysis plans Training
Experience5 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