Full Job Description
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 Senior Statistical Programmer 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:
Lead efforts in resolving day-to-day work-related issues and problems, ensuring quality of deliverables, as well as improving the efficiency and productivity of statistical programming work.
Lead assigned projects by applying project management skills and statistical programming techniques; achieve on-time delivery of deliverables with quality, as well as earn client's trust and repeat business.
Develop SDTM and ADaM dataset specifications for CSRs, ISS, and ISE following company's or client's Standard Operating Procedures (SOPs) and project specific requirements. Perform quality control (QC) review of these documents prepared by others.
Program and validate SDTM and ADaM datasets following approved dataset specifications for CSRs, ISS, and ISE.
Perform CDISC standard compliant checks on SDTM and ADaM datasets. Generate, review, and resolve Pinnacle 21 validation issues. Perform additional QC checks on these deliverables using company Working Instruction (WI) QC checklists.
Perform overall quality/consistency review of statistical TLGs before delivering them to the internal team or the client.
Create SDTM and ADaM define.xml files. Perform QC review of these files prepared by others.
Participate and/or lead programming teams in support of product regulatory submission related activities.
Learn and maintain expertise in the use of the utilities and macros developed for the Statistical Programmers. Develop new macros and utilities.
Program and perform QC/validation of complex data integrity checks to ensure data quality and ongoing scientific data surveillance.
Complete job-required and project-specific training. Comply with applicable Everest and trial Sponsor's Policies, SOPs, and WIs.
Document data and programming information in accordance with corporate SOPs and guidelines.
Archive clinical trial data (SDTM and ADaM datasets) and programming information in accordance with corporate archival SOPs and guidelines.
Qualifications:
A Master's or Ph.D. degree in Statistics, Biostatistics, Epidemiology, and Computer Sciences, with at least four years' experience in clinical trial statistical programming
OR
A Bachelor's degree in the above fields with at least six years' experience in clinical trial statistical programming.
Everest is inviting candidates to apply for this existing vacancy.
Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $90,000 - $140,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com.
We thank all interested applicants, however, only those selected for an interview will be contacted.
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