OnPoint Clinical Staffing Services Jobs

OnPoint Clinical Staffing Services

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Senior Clinical Research Associate at OnPoint Clinical Staffing Services

Chicago, IL | Full Time
$68k-89k (estimate)
11 Months Ago
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...

Senior Clinical Research Associate at OnPoint Clinical Staffing Services

Denver, CO | Full Time
$66k-86k (estimate)
11 Months Ago
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...

Senior Clinical Research Associate at OnPoint Clinical Staffing Services

Atlanta, GA | Full Time
$63k-83k (estimate)
11 Months Ago
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...

Senior Clinical Research Associate at OnPoint Clinical Staffing Services

Philadelphia, PA | Full Time
$68k-90k (estimate)
11 Months Ago
Job Description. Senior CRA. Responsibilities include. All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties. All aspects of site and registry management as prescribed in the project plans. Organize and make presentations at Investigator Meetings. Report, write...
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