California, North Carolina, Pennsylvania (United States Of America)
Vacancy Details
Vacancy posted by: Colorado Prevention Center
Job Title: Project Manager
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
Vacancy details
Vacancy description:
Job Code:
Project Manager
Job Title:
Project Manager
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
CRA
Country:
United States Of America
Location:
Colorado
Min experience:
5 years
Annual salary:
Negotiable
Apply by:
30 Nov 2008
Colorado Prevention Center
Job Title: Project Manager
Supervisor: Director, Research Operations
Responsibilities:
• 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.
Qualifications:
• 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%
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
Site by Redder