• JobLeads (Sterling, VA)
    … strategies 3) Develop strategic plans for company's product portfolios 4) Maintain clinical study documents and data management activities 5) Develop ... Preference will be given to candidates with recent experience in clinical and medical affairs management For the right leader, this is a wonderfully rewarding… more
    JobDiagnosis (07/05/18)
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  • AstraZeneca (Gaithersburg, MD)
    clinical trial activities Contribute and review Investigator Brochures (IB), protocols, clinical study reports, eCRF, informed consent forms etc. Review ... As a Medical Director Clinical Trial Safety Management (Gaithersburg, MD...ready narratives for medical accuracy for inclusion in the Clinical Study Reports Collaborates with other departments… more
    Ivy Exec (06/29/18)
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  • AstraZeneca Pharmaceuticals (Gaithersburg, MD)
    clinical trial activities *Contribute and review Investigator Brochures (IB), protocols, clinical study reports, eCRF, informed consent forms etc. *Review ... from all over the globe. As a Medical Director Clinical Trial Safety Management ( Gaithersburg, MD...ready narratives for medical accuracy for inclusion in the Clinical Study Reports *Collaborates with other departments… more
    HireLifeScience.com (06/29/18)
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  • JobLeads (Gaithersburg, MD)
    clinical trial activities * Contribute and review Investigator Brochures (IB), protocols, clinical study reports, eCRF, informed consent forms etc. * Review ... gout, systemic lupus and rheumatoid arthritis The Medical Director Clinical Trial Safety Management performs the safety...ready narratives for medical accuracy for inclusion in the Clinical Study Reports * Collaborates with other… more
    JobDiagnosis (07/05/18)
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  • Merck (Upper Gwynedd, PA)
    …- cycle. * Implements a Quality by Design approach from initial Protocol through Clinical Study Report. * Provides input and approves trial specific monitoring ... guidance of HQ CQM Lead, Director, the HQ CQM, AD will oversee clinical quality management within the Therapeutic Area supporting Clinical Trial Teams (for… more
    Healthjobsnationwide (07/19/18)
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  • GILEAD (Foster City, CA)
    …informed consents, case report forms, monitoring plans, abstracts, presentations, manuscripts and clinical study reports - May contribute to SOP development - ... Drug Safety and Public Health (DSPH) to ensure efficient management of study activities -Proactively identifies potential...regulations), ICH Guidelines, and GCP governing the conduct of clinical studies - Working knowledge and experience… more
    Healthjobsnationwide (07/18/18)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …operate a central sample management system. Works closely with cross-functional study team to implement and operationalize clinical trials. Supports the ... Operations department. This position is responsible for vendor (sample) management , provide input regarding strategy and oversee clinical... study teams and sub-teams. * Supports individual clinical study teams and biomarker sub-teams as… more
    Healthjobsnationwide (07/01/18)
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  • GILEAD (Foster City, CA)
    …and analysis of biomarker samples within a clinical trial - Provides sample management expertise to the Study Management Teams (SMTs) - Accountable for ... Skills for Position: - Must meet all requirements for Clinical Trials Management Associate (CTMA) position and...regulations), ICH Guidelines, and GCP governing the conduct of clinical studies - Working knowledge and experience… more
    Healthjobsnationwide (07/01/18)
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  • GILEAD (Foster City, CA)
    …in trainings for Clinical Trials Management Associates (CTMAs) and Clinical Project Assistants (CPAs), - For GS studies , assist in selecting Contract ... Skills for Position: - Must meet all requirements for Clinical Trials Management Associate (CTMA) position and...regulations), ICH Guidelines, and GCP governing the conduct of clinical studies - Working knowledge and experience… more
    Healthjobsnationwide (07/12/18)
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  • GILEAD (Foster City, CA)
    …with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and others Clinical , DSPH, Regulatory and Project Management staff to meet project ... data and data structure. Assists in the implementation of clinical data management process with vendors including...tracks, and resolves basic queries. Utilizes reports to track study progress and ensure timeliness and quality expectations are… more
    Healthjobsnationwide (07/03/18)
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  • Merck (Rahway, NJ)
    …changes the way we approach serious diseases. Under the general direction of a Clinical Safety and Risk Management (CSRM) Team Lead, the CSRM Physician is ... and/or vaccine safety and is responsible for the overall clinical risk management and safety surveillance of...to the development of new compounds and the further study of marketed compounds. * Partners with clinical more
    Healthjobsnationwide (07/11/18)
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  • Merck (Rahway, NJ)
    …changes the way we approach serious diseases. Under the general direction of a Clinical Safety and Risk Management (CSRM) Team Lead, the CSRM Principal Scientist ... professional and is responsible for contributing to the overall Clinical Risk Management and Safety Surveillance of...to the development of new compounds, and the further study of marketed compounds. * The CSRM Senior Principal… more
    Healthjobsnationwide (07/10/18)
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  • GILEAD (Foster City, CA)
    …resources experience. * Experience within a pharmaceutical/biotechnology organization is preferred. * Clinical operations or study management experience a ... Lead the design, development, and implementation of strategic learning programs across Clinical Operations. * Lead and guide new hire orientation, onboarding and… more
    Healthjobsnationwide (07/01/18)
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  • Otsuka Pharmaceutical (Princeton, NJ)
    …development planning, program management , and internal reporting. May directly supervise clinical management personnel. Serves as a member of the Clinical ... requested. Leads program level teams as Co-Chair and/or serves as lead clinical management representative for CRT/GBT/PDC/JDC/Alliance teams. Contributes to the… more
    Ivy Exec (06/26/18)
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  • Mirati Therapeutics (San Diego, CA)
    Clinical Operations departments to ensure data is CDISC/SDTM compliant. Represent Data Management as the clinical study database expert on Clinical ... SUMMARY: The Director of Clinical Data Management Operations will provide...according to timelines. Review all CDM documents within a study area to ensure a consistent approach Oversee the… more
    BioSpace (06/21/18)
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  • EMMES Corporation (Rockville, MD)
    …across six continents. We offer statistical support for the entire process of clinical trials from study design and protocol development through data analysis ... oral and written communication skills Prior experience with Good Clinical Data Management Practices Prior experience with...the critical elements for the development and execution of clinical trials or research studies Strong skills… more
    Washington Post (06/06/18)
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  • EMMES Corporation (Rockville, MD)
    …provides data management and statistical support for more than 200 clinical research studies , domestically and internationally. The VID group supports ... Monitor is responsible for completing study -specific data management activities in accordance with Good Clinical ...trial Assist in the planning, monitoring, and coordination of clinical research studies at external sites by… more
    Washington Post (05/20/18)
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  • Leidos Biomedical Research, Inc. (Frederick, MD)
    …information, and coordinating project activities associated with the monitoring functions of clinical studies - Assists with the review of protocols, informed ... Clinical Monitoring Research Program (CMRP) provides comprehensive, dedicated project management and clinical research to the National Institute of Allergy… more
    HireLifeScience.com (06/25/18)
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  • EMMES Corporation (Rockville, MD)
    …in collaboration with project teams is responsible for planning, monitoring, and coordinating clinical research studies at external study sites. As part ... collaboration, professional growth, and exceptional work life balance. Our studies impact public health initiatives on a global scale...We offer statistical support for the entire process of clinical trials from study design and protocol… more
    Washington Post (07/19/18)
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  • Merck & Co. (Upper Gwynedd, PA)
    …- cycle. * Implements a Quality by Design approach from initial Protocol through Clinical Study Report. * Provides input and approves trial specific monitoring ... guidance of HQ CQM Lead, Director, the HQ CQM, AD will oversee clinical quality management within the Therapeutic Area supporting Clinical Trial Teams (for… more
    HireLifeScience.com (07/19/18)
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