Careers
CPC 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 Careers, CPC, 13199 E. Montview Blvd., Suite 200, Aurora, CO 80045. Fax (303-860-1288) or e-mail (Careers@cpcmed.org ) will be accepted.
Current Openings:
Receptionist
Associate Director Biostatistics / Lead Biostatistician
Supervisor: Director of Business Operations
Responsibilities:
- Greet visitors, and notify the appropriate employee of their arrival
- Have visitors sign the sign in sheet and issue a visitor badge
- Filter incoming phones calls and route to appropriate employee
- Perform general administrative tasks such as document preparation, filing, copying, scanning, and faxing
- Order office supplies and help maintain inventories
- Keep lobby looking orderly
- If scheduled in the morning, empty both dishwashers and ensure break areas are tidy
- Manage outgoing mail and distribute incoming
- Assist with mass mailings
- Keep fresh supply of coffee for visitors and staff, as well as stock refrigerator
- Order FedEx and UPS supplies
- Other duties as required
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Good interpersonal communication skills, good organizational skills and good attention to detail are required.
- Good computer skills and experience with Microsoft Office Suite (Word, Excel, Outlook)
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This individual must be able to work as a member of a team.
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Job Title: Associate Director of Biostatistics / Lead Biostatistician
Supervisor: Director of Biostatistics & Data Management
Date: August 2010
CPC Clinical Research is an Academic Research Organization dedicated to the management of clinical trials with the highest levels of quality and integrity. Competitive salary and benefits package, flexible schedules, and on-site exercise facilities.
Responsibilities:
- Participate as lead biostatistician on project teams.
- 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.
- Mentor and teach new skills to biostatistician and programming staff.
- 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).
- 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
- 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.
- Develop positive and effective working relationship with project team members (project manager, data managers, other biostatisticians, Sponsors).
- Perform other duties as may be required by CPC management.
Qualifications:
- Ph.D. 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).