Medical & Health Jobs

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Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Riverside | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Richmond | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Sacramento | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Salinas | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure San Bernardino | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure San Francisco | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure San Jose | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Santa Barbara | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Santa Rosa | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure South Lake Tahoe | Medical & Health | Added: Apr 27, 2008 | Confidential
Clinical Trial Manager/Project Manager 1) Assist with designing, planning and implementation of clinical research projects 2) Manage the development of protocols, CRFs, ICFs, study manuals and study budgets 3) Negotiate and finalize site contracts and budgets 4) Manage and calculate site payments 5) Perform site visits, including site qualification, initiation, monitoring and closeout visits 6) Hire, train and supervise regional monitors and review monitoring reports 7) Ensure that the sites comply with study protocol (to ensure Stockton | Medical & Health | Added: Apr 27, 2008 | Confidential
Quality Assurance Professional Responsibilities include: Managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. This position will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.Background: BSc is the minimum education level accepted for this position. Previous experience in research required; oncology experience preferred. Good Los Angeles | Medical & Health | Added: Apr 22, 2008 | Espoirbridge
Quality Assurance Professional Responsibilities include: Managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. This position will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.Background: BSc is the minimum education level accepted for this position. Previous experience in research required; oncology experience preferred. Good San Diego | Medical & Health | Added: Apr 22, 2008 | Espoirbridge
Quality Assurance Professional Responsibilities include: Managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. This position will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.Background: BSc is the minimum education level accepted for this position. Previous experience in research required; oncology experience preferred. Good San Jose | Medical & Health | Added: Apr 22, 2008 | Espoirbridge
Quality Assurance Professional Responsibilities include: Managing and planning regulatory affairs compliance for industry sponsors and/or sites in networks. This position will work closely with the regulatory affairs management, department director and/or primary investigators to ensure compliance, preparing for auditing activities while meeting strict deadlines.Background: BSc is the minimum education level accepted for this position. Previous experience in research required; oncology experience preferred. Good San Francisco | Medical & Health | Added: Apr 22, 2008 | Espoirbridge
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