Biostatistician

4 months ago

Markham, Canada Everest Clinical Research Full time

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, and Shanghai (Pudong Zhangjiang New District), China.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength that’s us that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as **Biostatisticians **for our Toronto/Markham, Ontario, Canada on-site location, or remotely from a home-based office anywhere in Canada in accordance with our Work from Home policy.

**Key Accountabilities**:
**Leadership and Project Management**:

- Participate and/or lead efforts in resolving day-to-day work-related issues and problems, securing quality, and improving efficiency and productivity of statistical and programming operations.
- Assist the Lead Biostatistician and/or Lead Programmer for a developmental program with more than one or two trials, coordinating with other Biostatisticians and Programmers, as well as project/program overall management personnel, to achieve program objectives.

**Statistical Planning and Methodologies**:

- Under supervision, provide statistical expertise for design, analysis, and reporting of clinical trials and research projects.
- Write statistical sections of study protocols, perform sample size calculation, develop randomization specifications, and generate randomization codes.
- Write Statistical Analysis Plans (SAPs) and properly address quality control (QC) review comments.
- Create and maintain Statistical and Programming QC and Quality Assurance Plans for assigned projects or programs.
- Provide input to unblinded data management plan when required.
- Participate in research and development of statistical methodologies and processes.

**Statistical Programming**:

- Develop and/or review SDTM and ADaM dataset specifications.
- Perform statistical programming to either build analysis datasets and generate statistical tables, listings, and graphs (TLGs) or perform QC validation of these datasets and TLGs.
- Participate in statistical dry runs and final run by actively participating or contributing to project and resources management, addressing statistical and programming questions and interacting with data management to follow-up and resolve data issues.
- Develop SDTM Study Data Reviewer’s Guide, discuss and incorporate Data Standards Reviewer’s review comments to ensure quality of the document.
- Develop ADaM Analysis Data Reviewer’s Guide, discuss and incorporate Data Standards Reviewer’s review comments to ensure quality of the document.

**Statistical Analysis and Reporting, Publication Support**:

- Perform statistical modeling and analyses, implement new statistical analysis methods and strategies.
- Perform statistical analysis as per SAP, and address peer/QC review comments and findings.
- Perform statistical validation of study results, address additional QC validation comments and findings on the results.
- Plan and conduct or contribute to the trial results reporting/dissemination meetings.
- Contribute to the contents describing any deviation from the planned analysis and deviation from study conduct for the Clinical Study Report (CSR). Review CSR to ensure accuracy, completeness, and appropriateness of the interpretation of the statistical results.
- Write statistical report or statistical sections of the CSR or perform peer review of the contents.
- Perform statistical analyses for publications, including but not limited to abstracts, manuscripts, presentations, and posters.

**Supporting Clinical Data Collection and Cleaning**:

- Provide statistical input to Case Report Forms (CRF) design and database/variable structure.
- Provide statistical input to non-CRF data collection and acquisition methods and approaches.
- Review Data Management Plan sections relating to critical data collection and cleaning. Provide statistical input to Data Validation Specification.

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