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If you are a highly motivated individual who has a strong desire to work in all phases of drug development and in multiple therapeutic areas then read on. You could become part of a high performing team at Everest Clinical Research. With over ten years in the pharmaceutical industry, our focus on high quality delivery, customer satisfaction, and continuous development of our staff has enabled strong business growth. To drive continued success in the global marketplace, we are looking for committed, skilled, and customer-focused individuals to join our winning team.

As we continue to expand our business, we are currently seeking a qualified and highly motivated individual to work in our Markham office as a Statistical SAS Programmers.


Statistical SAS Programmer


Key Responsibilities:

The Clinical Trial Safety Associate is responsible for the overall case processing and management of serious adverse events (SAEs) and device incident (DI) reports in compliance with Everest standard operating procedures (SOPs) and regulatory guidelines related to pharmacovigilance (PV) and medical device vigilance (MDV) activities for our clients. This includes, but is not limited to, case assessment, data entry and query generation, data reconciliation, narrative writing, interactions with clinical study sites, and overall management of cases. This individual will work closely with multidisciplinary study teams in all aspects of safety data processing, management, and reporting The Statistical Programmer will develop SAS codes to create accurate, complete and efficient statistical analysis datasets; and to generate statistical analysis output tables, listings and graphs. Quality control programming validation procedures will be performed and documented by the incumbent. The incumbent will also program for database integrity checks and work closely with Clinical Data Managers and Quality Assurance personnel to assure database quality. These programming supports will be provided in compliance with relevant Corporate Standard Operating Procedures and Good Working Practices.

Qualifications and Experience:

A masters’ degree in Computer Science or Mathematics and Statistics, with SAS programming experience on PC/Unix platforms is required. Solid understanding of clinical drug development process and knowledge of FDA regulatory requirements and ICH/GCP guidelines is preferred.

Senior Statistical SAS Programmer


Key Responsibilities:

The Senior Statistical Programmer will have several years experience working as a Statistical Programmer performing similar duties as described above. Additionally, the incumbent will resolve complex programming problems and provide oversight to other Statistical Programmers; lead efforts in the development, maintenance and adherence of Corporate policies, SOPs, and therapeutic area specific guidelines; may act as a Lead/Liaison Programmer, interacting with clinical trial sponsors and oversee projects in given therapeutic areas

Qualifications and Experience:

A masters’ degree in Statistics or Computer Science, with at least 6 years experience in support of clinical trial data analysis and reporting, and demonstrated leadership ability to effectively manage statistical programming activities and integrate them with the entire clinical trial operations.

We are an equal opportunity employer. We thank all interested applicants; however, only those selected for an interview will be contacted.

How to Apply

Please send your application, indicating the position to which you are applying to careers@ecrscorp.com.

Posting Date: February 17, 2015

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