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Senior Biostatistician (FSP)

76% Flex
EXTRA HOLIDAYS
Remote: 
Full Remote
Contract: 
Salary: 
123 - 233K yearly
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

PhD or MS in Statistics/Biostatistics, 5+ years industry experience, Regulatory submission experience, Strong SAS and/or R skills, Experience with simulations.

Key responsabilities:

  • Provide statistical support for drug development programs
  • Interact with project teams to establish timelines
  • Write statistical sections of clinical trial protocols
  • Monitor project activities and review study results
  • Collaborate on design of eCRFs and regulatory documents
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IQVIA Health Care Large https://www.iqvia.com/
10001 Employees
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Job description

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Your missions

Job Level: Senior Biostatistician within DSSS

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 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 opportunities
  • Work/life balance as well as flexible schedules
  • Collaborating with dedicated, high-performance, statistical and research teams
  • Variety of therapeutic areas, indications and, study phases
  • 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.

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 submissions
  • Successful 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 methods
  • Knowledge of simulations, multivariate analyses, and biomarker analyses

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IQVIA 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 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 $122,800.00 - $233,400.00. 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.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Health Care
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Soft Skills

  • Supervisory Skills
  • Effective Communication
  • Team Collaboration
  • Business Decision Making

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