Careers

The CPC, located in downtown Denver, Colorado, provides a great environment in which to work.

If you are interested in applying for any of the positions below, please send CV, cover letter and 3 references to Sandy Brinks, Colorado Prevention Center, 789 Sherman, Suite 200, Denver, CO 80203. Fax (303-860-1288) or e-mail (Careers@cpcmed.org ) will be accepted.

Current Openings:

Job Title: Senior Biostatistician/Associate Director or Director of Biostatistics

Supervisor: TBD

Date: January 12, 2010

Responsibilities:

• Participate as lead biostatistician on project teams.
• Develop positive and effective working relationship with project team members (project manager, data managers, other biostatisticians, Sponsors).
• Participate in the design, writing and review of statistical analysis plans and study protocols.
• Analyze and manage data in SAS and other statistical packages.
• Prepare, review, and submit final clinical study reports, including NDAs.
• Analyze data for, and prepare and review interim study reports, manuscripts, abstracts, and grants.
• Ensure that study protocols, statistical programs, analyses and reports generated within the CPC comply with GCP, FDA, and ICH guidelines and CPC standards.
• Provide general statistical support and consulting services.
• Develop and review statistical standard operating procedures (SOPs).
• Academically participate in the field of biostatistics/clinical trials through membership in related professional organizations, making presentations at professional conferences, and/or submissions to relevant journals.
• Oversee quality and accuracy of the work of biostatisticians and SAS programmers
• Help mentor and teach new skills to biostatistician and programming staff.
• Provide weekly feedback to the Director of Biostatistics & Data Management on the progress of projects
• Assist Director with project oversight and management of project teams.
• Review CRFs for statistical integrity.
• Participate in the review of the design and validation of study database software and related database queries.
• Perform other duties as may be required by CPC management.

Qualifications:

• Ph.D. or Master's degree in biostatistics or related field, and a minimum of 5 years experience in the analysis of data for clinical trials.
• Must have experience with FDA/NDA submissions.
• Must have leadership ability and experience, including at least 1 year supervisory experience.
• Demonstrable programming experience with SAS 9.0 or higher in a Windows environment.
• Must possess excellent analytical, organizational, communications, and team skills, and be detail oriented.
• Experience with Microsoft Office (Word, Excel, PowerPoint).