Offer summary

Qualifications:

PhD in Statistics, Biostatistics, or related field with 5+ years of industry experience, or MS with 7+ years., Strong early phase (Phase I) experience is required., Proficiency in SAS and/or R for efficacy analyses and data validation., Understanding of ICH GCP, ICH E9, and experience with CDISC standards..

Key responsabilities:

Collaborate with project teams to set objectives and timelines.

Write statistical sections of clinical trial protocols and analysis plans.

Monitor project activities and provide guidance to programming teams.

Interpret study results and contribute to clinical study reports and regulatory documents.

Job description

Job Responsibilities:

· Collaborate with multi-disciplinary project teams to establish project objectives and timelines.

· Write 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.

· Collaborate with Data Management, Clinical Development, and Clinical Operations with statistical expertise.

· Contribute 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.

· Strong early phase (Phase I) experience .

· Demonstrated 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

Desired Experience:

· Familiarity with R programming language and other statistical software.

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

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