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Senior Biostatistician

Job Description

Our client is currently seeking a driven and ambitious Senior Biostatistician to join their team. This is a unique opportunity for a highly motivated professional who has a go-getter attitude.

1) Ensure that product and study level deliverables are completed on time, of high quality, and in accordance with company, industry and regulatory requirements
2) Set up and maintain SAS programming infrastructure in support of complex clinical trial reporting and submission activities
3) Offer SAS programming support for a variety of activities including but not limited to creating outputs for integrated analyses, clinical study reports, safety monitoring, manuscripts, conferences, ad hoc analyses and exploratory analyses
4) Work with the Clinical Affairs team to establish project requirements
5) Collaborate with functional management across the organization on project deliverables and timelines for projects within area of responsibility
6) Oversee all programming support activities for a clinical program in line with acceptable statistical methodology, timely and accurate data integration, analysis and interpretation of results
7) Oversee the preparation and review of programming deliverables for clinical study reports and scientific presentations and participate in team review of documents
8) Co-ordinate with all Data Management Data Review activities and any other Clinical Study Team Data Review
9) Determine documentation and archival standards of statistical programming deliverables including analysis databases, summaries, programs, and specifications
10) Manage department quality requirements in co-ordination with Regulatory Affairs, Quality Assurance and Information Technology
11) Work with Information Technology in determining computer system resources and database infrastructure requirements
12) Develop, apply and promote consistent programming standards through standard processes and SOPs
More questions? Want to know the Salary range? Keep reading.

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TAGS: Biotechnology Jobs, Pharmaceutical Jobs, Medical Device Jobs, Small Molecule, Biologic, Oncology, Hematology, Dermatology, Neurology, Cardiology, Urology, Nephrology, Vaccine, Disease, Drug Development, Surgery, Physician, EMR, Healthcare, Life Sciences, Scientist, R&D, Clinical Research, Clinical Trial, Regulatory Affairs, Nutraceutical, Surgeon, MD, Hospital, Immunology, Quality, QC, Validation, Engineer, QA, Manufacturing, Engineering, Aseptic, Sterility, Hospital, Research and Development, Medical Affairs, Drug Safety

Job Requirements

1) University degree is required (preference will be given to those with degree in relevant field, though all candidates are welcome and encouraged to apply)
2) Appropriate full-time work experience is mandatory (no students or fresh graduates please)
3) Recent experience in the medical device industry is strongly preferred
4) Preference will be given to people have recent experience in data management

This position is critical to the team and requires a qualified individual to fill the role... someone with a real go-getter attitude!

Job Snapshot

Post Date 4/13/2014
Location Los Angeles, CA
Employment Type Full-Time
Job Type Management
Education Not Specified
Experience Not Specified
Manages Others Not Specified
Industry Biotechnology, Pharmaceutical, Medical Equipment
Required Travel Not Specified
Job ID USA-137
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