Source One is a consulting services company and we’re currently looking for the following individual to work as a remote consultant to our direct client, a global medical device company.
Job Title: Statistical Consultant
Duration: 24 months
40 hours/week, Mon-Fri, 1st shift
Job Description:
- Lead the statistical design and analysis of projects, collaborating closely with cross-functional teams, to establish the conditions essential for determining safety, efficacy, and marketability of investigational products.
- Review and contribute to study protocols, statistical analysis plans, and clinical study reports, adhering to regulatory guidelines and industry best practices.
- Develop and implement advanced statistical methodologies and models, ensuring appropriate implementation to address project needs in one or more Therapeutic or Technology Areas.
- Analyze and interpret clinical trial data, including efficacy and safety endpoints, and provide actionable insights to support decision-making.
- Collaborate with statisticians, data scientists, and programmers to ensure the accurate and timely delivery of statistical outputs for regulatory submissions and scientific publications.
- Conduct exploratory data analysis, including use of visualization and statistical techniques to identify trends, patterns, and potential safety signals in clinical trial data.
- Participate in meetings with regulatory authorities, addressing statistical queries and providing necessary documentation for submissions.
Minimum Requirements
- Advance degree in Statistics or related discipline
- At least 3 years’ experience supporting the design and analysis of clinical trials in a Medical Device or Pharmaceutical company
- SAS programming experience is a must, R programming experience is a plus
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