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:

Project Manager

Clinical Research Associate II or Sr. Clinical Research Associate

Job Title: Project Manager
Supervisor: Director, Research Operations

• Serve as the primary point of contact for industry sponsored clinical trials, as well as any additional assigned projects.
• Develop and manage multidisciplinary project team members related to project management activities. Schedule, plan for, and document regularly scheduled project team meetings. Assess project issues, propose resolutions to the project team, CPC executives and/or the Sponsor, and then track implementation of resolution through to completion.
• Define and monitor project scope, timelines and deliverables from project initiation to close out. Assist in study site selection, initiation and monitoring as required by project. Provide drug tracking and disposition as needed as required by project.
• Ensure the overall quality of project services and deliverables.
• Participate in the design, writing and review of all project-related documents including: budgets and proposals, change orders, and study content documents including protocols, case report forms, statistical analysis plans, study reports and monitoring documents.
• Provide status reports on all projects as necessary.
• Assist in IRB issues.
• Track and request study site payments.
• Provide necessary updates and reports to the Sponsor as outlined by the contract.
• Additional activities as required.
• Supervise and evaluate performance of all staff reporting to this position.

• BA/BS in a scientific field.
• A minimum of 5 years experience in medical research or related field and a minimum of 2 years clinical research project management experience.
• Thorough knowledge of the Good Clinical Practice guidelines and the applicable FDA and ICH regulations for conducting clinical drug trials.
• Experience with MS Office including Access, Word and Excel.
• Excellent interpersonal communication skills, organizational skills and a great attention to detail are required. This individual must be able to work as a member of a team and possess good problem solving skills.
• Possesses the ability to organize, instruct and supervise staff, while promoting group effort and achievement.
• Ability to manage conflicts and resolve problems effectively.
• Ability and willingness to travel up to 25%.

Job Title: Clinical Research Associate II or Senior Clinical Research Associate
Supervisor: TBD

Job Description:

A unique and exciting opportunity to work as a full-time CRA II or Senior CRA. Regional positions will be considered for exceptional candidates.

• Positions involve site support and monitoring for multi-center clinical trials according to standard operation procedures, Good Clinical Practice guidelines and applicable regulations.
• Other responsibilities include specialized endpoint evaluation site visits to ensure appropriate collection of endpoint data.
• Position will also be involved in hands-on training of site staff, CRAs and Sponsors.
• Up to 60% travel.
• Potential for international travel.
• Full benefits package.

• Minimum 3 years experience in clinical trials research and minimum 2 years monitoring experience.
• Experience with health care and training/mentoring skills are a plus.
• Thorough knowledge of the Good Clinical Practice guidelines and the applicable FDA and ICH regulations for conducting clinical drug trials.
• Computer skills to include spreadsheet databases and word-processing.
• Exceptional interpersonal communication skills and organizational skills, and great attention to detail are all required.
• Must be able to work as a member of a team and possess excellent problem solving skills.

Bachelor’s degree, RN, BSN, or an Associate’s Degree with clinical research experience.