• JobLeads (Fairfax, VA)
    …Virginia, Required Qualifications: *Project management training or experience, or event planning experience *Formal education in health, behavioral or social ... physicians and med Thu, 18 Oct 2018 11:02:07 EST http://careers.aencnet.org/jobs/11593928/certification- coordinator http://careers.aencnet.org/jobs/11593928/certification- coordinator Alexandria, Virginia, The Certification … more
    JobLeads (10/23/18)
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  • JobLeads (Falls Church, VA)
    …Virginia, Required Qualifications: *Project management training or experience, or event planning experience *Formal education in health, behavioral or social ... Requires excellent w Tue, 02 Oct 2018 10:27:46 EST http://careers.psae.org/jobs/11551903/sections-divisions- coordinator http://careers.psae.org/jobs/11551903/sections-divisions- coordinator Arlington Va-Clarendon (Orange line) Metro,… more
    JobLeads (10/24/18)
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  • Merck (Upper Gwynedd, PA)
    …radically changes the way we approach serious diseases. This position is a coordinator /support role for the scientific conduct of a protocol. Assists the Protocol ... position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other… more
    Healthjobsnationwide (11/15/18)
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  • Covance (Los Angeles, CA)
    …with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up ... employees, eg co-monitoring Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client… more
    Healthjobsnationwide (11/05/18)
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  • Covance (Princeton, NJ)
    …with statements of agreements as assigned Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of ... employees, eg co-monitoring Co-ordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client… more
    Healthjobsnationwide (11/05/18)
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  • TKL Research, Inc. (Fair Lawn, NJ)
    …Dermatologist will collaborate with the Department Director/Clinical Research Coordinator . Ensure medical follow up during the study (inclusion/exclusion ... the study according to the protocol. In case of a significant adverse event during a study, the Dermatologist is responsible for the appropriate notifications and… more
    Neuvoo (11/09/18)
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  • JobLeads (Wheaton, IL)
    …Bay Area; Southern http://careers.aencnet.org/jobs/11567772/chapter-outreach- coordinator San Diego, QUALIFICATIONS: ... Skill and Ability: Bachelor's degree required; 8-10 years' experience in meeting and/or event planning and executing large, complex meetings, with de Wed, 03 Oct… more
    JobLeads (10/27/18)
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  • JobLeads (Lake Mary, FL)
    …10:27:46 EST http://careers.aencnet.org/jobs/11563961/membership-marketing- coordinator http://careers.aencnet.org/jobs/11563961/membership-marketing- coordinator ... three years' experience in association/non-profit management and marketing; including meeting and event management, working with board of dir Thu, 11 Oct 2018… more
    JobLeads (10/23/18)
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  • Watson Health Biomedical Research…

    IBM (Bethesda, MD)
    …is Boston, MA, New York, NY or Nashville, TN.** The **Biomedical Research Coordinator ** is responsible for the design, authoring, and conduct of research protocols ... and guidelines; and institutional partner policies and procedures. The research coordinator manages research study conduct from study design through study closeout,… more
    IBM (11/13/18)
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  • Pharmacy Operations Coordinator

    Johns Hopkins Medicine (Baltimore, MD)
    …The Pharmacy Operations Coordinator reports to the Pharmacy Manager. In the event the Pharmacy Manager is not available, the Pharmacy Operations Coordinator ... Job Details APPLY REFER A FRIEND BACK **Pharmacy Operations Coordinator ** **Requisition #:** 172923 **Location:** Johns Hopkins Home Care Group, Baltimore, MD… more
    Johns Hopkins Medicine (09/14/18)
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  • Clinical Research Coordinator - Radiology

    Duke University (Durham, NC)
    …107116BR **Duke Entity:** MEDICAL CENTER **Job Code:** 1201 CLINICAL RESEARCH COORDINATOR **Job Description:** **Occ Summary** Participate in or lead day-to-day ... IP compliance at the protocol-and subject level. Collect, prepare, or process adverse event information per protocol, and provide input for adverse event more
    Duke University (11/16/18)
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  • Compliance and Product Management…

    Providence Health & Services (Beaverton, OR)
    **Description:** **Providence is calling a Compliance and Product Management Coordinator to Providence Health Plan in Beaverton, OR.** **In this position, you ... type of product offered by PHP. + Lead implementation coordinator for all new custom pharmacy benefits and pharmacy...and processes in place for contingency needs in the event of natural or other health care related disasters… more
    Providence Health & Services (10/19/18)
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  • Clinical Research Coordinator

    Duke University (Durham, NC)
    …**Duke Entity:** MEDICAL CENTER **Job Code:** 1201 CLINICAL RESEARCH COORDINATOR **Job Description:** OBGYN-Division of Maternal-Fetal Medicine Clinical Research ... Coordinator **Operations:** Screen participants for all studies independently. May...and study audit visits. Collect, prepare or process adverse event information independently. Complete and submit AE Reports, according… more
    Duke University (10/07/18)
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  • Clinical Research Coordinator

    Duke University (Durham, NC)
    …**Duke Entity:** MEDICAL CENTER **Job Code:** 1201 CLINICAL RESEARCH COORDINATOR **Job Description:** **Operations:** Screen participants for minimal risk studies. ... monitoring and study audit visits. Collect, prepare or process adverse event information under supervision. Complete and submit Adverse Events Reports, according… more
    Duke University (11/09/18)
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  • Manufacturing Coordinator / Sr.…

    Catalent Pharma Solutions (San Diego, CA)
    …Qualified candidates will be hired at the appropriate level (Associate, Coordinator , Senior) commensurate with required education and years of required relevant ... as needed. Ensures timely completion and closure of quality event documentation. + While working on a project team,...relevant experience. + To qualify for a Senior Manufacturing Coordinator , candidates will have a minimum of 5 years… more
    Catalent Pharma Solutions (11/06/18)
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  • Clinical Research Coordinator

    Duke University (Durham, NC)
    …**Duke Entity:** MEDICAL CENTER **Job Code:** 1201 CLINICAL RESEARCH COORDINATOR **Job Description:** **Operations:** Screen participants for all studies ... study monitoring and study audit visits. Collect,prepare or process adverse event information independently Complete and submit AE Reports,according to institution… more
    Duke University (10/10/18)
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  • Manager, Americas Regional Compliance

    Teva Pharmaceuticals (Parsippany, NJ)
    …management, metrics, inspection management, quality systems, and critical event lifecycle management (FARs). **Responsibilities** **Americas Region Liaison** + ... to ensure timely internal communication for all elements of a critical event , supports investigational process for critical events, and facilitates the incident to… more
    Teva Pharmaceuticals (10/05/18)
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  • FSP - Sr. Clinical Research Associate - Oncology

    Covance (Cleveland, OH)
    …with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up ... employees, eg co-monitoring + Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client… more
    Covance (11/16/18)
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  • Sr. Clinical Research Associate - ONC

    Covance (San Francisco, CA)
    …with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up ... employees, eg co-monitoring + Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client… more
    Covance (10/04/18)
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  • Senior CRA - Germany

    Covance (DE)
    …with statements of agreements as assigned + Complete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of ... employees, eg co-monitoring + Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client… more
    Covance (08/26/18)
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