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Clinical Research Management, Inc.
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4/29/2013
Clinical Research Management, Inc.
Frederick, MD

Growing and well-respected biomedical (clinical, basic and applied) research firm has openings at USAMRIID. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong...

4/26/2013
Clinical Research Management, Inc.
Jacksonville, FL

ClinicalRM is seeking a Research Assistant to work at NHJAX in Jacksonville, FL.RESPONSIBILITIES:1. Execute and provide maintenance on research studies. Carry out tasks related to research studies as required by investigator.2. Maintain files and...

4/26/2013
Clinical Research Management, Inc.
Camp Lejeune, NC

ClinicalRM is seeking a Research Assistant to work at NHCL in Camp Lejeune, NC.RESPONSIBILITIES:1. Execute and provide maintenance on research studies. Carry out tasks related to research studies as required by investigator.2. Maintain files and...

4/26/2013
Clinical Research Management, Inc.
Portsmouth, VA

ClinicalRM is seeking a Research Assistant to work at NMCP in Portsmouth, VA.RESPONSIBILITIES:1. Execute and provide maintenance on research studies. Carry out tasks related to research studies as required by investigator.2. Maintain files and...

4/26/2013
Clinical Research Management, Inc.
Portsmouth, VA

ClinicalRM is seeking a Clinical Research Nurse Coordinator to work at NMCP in Portsmouth, VA.RESPONSIBILITIES:1. Recruit and screen patients using protocol inclusion/exclusion criteria. Refer eligible patients to the PI for final evaluation.2. ...

4/26/2013
Clinical Research Management, Inc.
Portsmouth, VA

ClinicalRM is seeking a Clinical Research Coordinator to work at NMCP in Portsmouth, VA.RESPONSIBILITIES:1. Responsible for coordinating the research activities of assigned IRB-approved study protocols. Specific protocols that require the CRC's...

4/26/2013
Clinical Research Management, Inc.
Portsmouth, VA

ClinicalRM is seeking a Compliance Officer to work at NMCP in Portsmouth, VA.RESPONSIBILITIES:1. Audits research investigator activities on site.2. Reviews IRB approved protocols and interviews investigators to assure compliance is met.3. Reviews...

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