• Clinical Evaluation Manager

    Olympus Corporation of the Americas (Center Valley, PA)
    …Close collaboration with Product Management, Risk Management, R&D and Regulatory Affairs to provide input on deliverables, clinical research and literature ... purpose and our core values by staying **True to Life.** **Job Description** The Clinical Evaluation Manager reports directly to the Regional Lead, Clinical more
    Olympus Corporation of the Americas (04/10/24)
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  • Associate Clinical Research Manager

    Merck (Columbus, OH)
    …+ Collaborates internally with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilance, Regulatory Affairs , Global Medical ... **Job Description** **Position Description:** **Associate Clinical Research Manager (aCRM) - Oncology**...the TA-Head or CRD. + Requires understanding of local regulatory environment. + Scientific and clinical research… more
    Merck (04/26/24)
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  • Regional Clinical Study Manager

    BeiGene (Emeryville, CA)
    …in assigned region in close collaboration with regional study start up team and regulatory affairs + Ensures regional and country information in study systems ... progress in the region to senior management and Global Clinical Study Manager as required + Represents...region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders + Provides regional input… more
    BeiGene (03/23/24)
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  • Sr. Clinical Research Program…

    Johns Hopkins University (Baltimore, MD)
    …+ Requires minimum of two years of management experience. + Requires experience in clinical research and regulatory affairs . + Experience in protocol and ... the division. The Sr. Clinical Research Program Manager will be responsible for ensuring regulatory ...and/or clinical trials. + Requires experience in clinical research and regulatory affairs more
    Johns Hopkins University (02/28/24)
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  • Project Manager Clinical Research…

    Dignity Health (Phoenix, AZ)
    …!** **This position will be responsible for steering the regulatory affairs of a groundbreaking multi-center clinical study in translational ALS research. ... Clinical Research Regulatory Project Manager...high attention to detail and subject matter expertise in Clinical Research Regulatory Affairs management… more
    Dignity Health (04/03/24)
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  • Senior Manager - Clinical Science

    Abbott (Pleasanton, CA)
    clinical trial design, by collaborating closely with the statistician, medical affairs , and regulatory affairs personnel, that appropriately satisfy the ... schedules while enhancing productivity and product quality. **THE OPPORTUNITY** **Senior Manager , Clinical Science** We have an exciting opportunity for… more
    Abbott (04/25/24)
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  • Manager , Clinical Research

    University of Miami (Miami, FL)
    …the efforts of relevant team members to manage, retain and control all applicable Regulatory Affairs submissions pertaining to University held INDs and IDEs as ... . The Department of Pathology and Laboratory Medicine is currently seeking a full time Manager , Clinical Research to work in Miami, FL. The Manager , … more
    University of Miami (04/16/24)
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  • Clinical Quality Assurance Manager

    Olympus Corporation of the Americas (Center Valley, PA)
    Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Pennsylvania (US-PA) || Center Valley || Quality & Regulatory Affairs (QA/ RA ) ... purpose and our core values by staying **True to Life.** **Job Description** The Clinical Quality Assurance Manager reports directly to the Executive Director of… more
    Olympus Corporation of the Americas (03/09/24)
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  • Clinical Research Project Manager

    Dignity Health (Phoenix, AZ)
    …with organizational goals.. * Collaborate with internal cross-functional teams, including clinical operations, data management, regulatory affairs , and ... therapies for brain tumor patients. Job Description: The Ivy Clinical Research Project Manager is responsible and accountable for providing the coordination and… more
    Dignity Health (04/12/24)
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  • Senior Project Manager , Clinical

    Abbott (Maple Grove, MN)
    …and exchange of documents between stakeholders (eg, internal personnel such as Regulatory Affairs , R&D Engineering, Clinical Engineering, A&P and ... MN currently has an opportunity for a **Senior Project Manager , Clinical Evaluation** . This new team...5-7+ years of experience in clinical research, clinical affairs , regulatory affairs more
    Abbott (02/21/24)
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  • Clinical Research Program Manager

    Johns Hopkins University (Baltimore, MD)
    …+ Requires minimum of one year of management experience. + Requires experience in clinical research and regulatory affairs . + Experience in protocol and ... financial management of clinical trials preferred. Classified Title: Clinical Research Program Manager Role/Level/Range: ACRP/04/MD Starting Salary Range:… more
    Johns Hopkins University (04/26/24)
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  • Senior Manager Clinical

    AdventHealth (Maitland, FL)
    …**The role you'll contribute:** The Population Health Services Organization (PHSO) Senior Manager of Clinical Documentation Integrity (CDI) will be responsible ... range of risk adjustment coding services for the AdventHealth Population Health Ri Clinical Documentation Integrity Program. This will include but not be limited to… more
    AdventHealth (04/04/24)
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  • Senior Clinical Research Business Process…

    Medtronic (North Haven, CT)
    Senior Clinical Research Business Process Improvement Manager ...conduct of clinical studies and for the regulatory affairs function as it applies to ... this exciting role as Senior Clinical Research Manager in the Surgical Operating Unit, you will be...+ Studies must be scientifically valid, meet all relevant regulatory requirements and be conducted within ethical guidelines. +… more
    Medtronic (04/27/24)
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  • Sr. Clinical Study Manager

    Kedrion Biopharma, Inc. (Fort Lee, NJ)
    …literature and attending courses/seminars. **Relations/Network** + Interacts internally with Global Clinical Research and Operations, Regulatory Affairs , ... retention materials, in conjunction with any partner CRO project manager . + **Delivery of Clinical Trial** -...to resolution. May include preparation for and participation in regulatory inspections of selected clinical trials. +… more
    Kedrion Biopharma, Inc. (01/30/24)
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  • Clinical Operations Manager

    Merck (Columbus, OH)
    …+ Works in partnership internally with GCTO country operations, finance, regulatory affairs , pharmacovigilance, legal and regional operations, HQ functional ... country information in clinical and finance systems. + Ownership of local regulatory and financial compliance. The position has a significant impact on how a… more
    Merck (04/17/24)
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  • US Regulatory Affairs - GDP,…

    System One (Florham Park, NJ)
    Position: CONTRACTOR -- US Regulatory Affairs - GDP, RA , Associate Location: Remote (East or Central Time Zone) Contract: 12mns Pay Rate: 25/hr - 35/hr This ... Biochemistry) preferred. + Minimum of 2 years of Pharmaceutical industry experience in Clinical Development Operations or Regulatory Affairs preferred. +… more
    System One (03/06/24)
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  • Pharmacovigilance Manager , Clinical

    Boehringer Ingelheim (Ridgefield, CT)
    …training and resource planning in collaboration with Clinical Operations, Medical Affairs , BDS, HEOR, Global Regulatory Affairs , Commercial teams, etc. ... Biostatistics and Data Sciences (BDS), Health Economics Outcomes Research (HEOR), Global Regulatory Affairs , Commercial/Marketing teams, etc. in areas of adverse… more
    Boehringer Ingelheim (03/01/24)
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  • Clinical Research Associate I

    Abbott (Alameda, CA)
    …study site staff, and clinical management. + Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs + Flexibility in daily activities. + ... for completeness and accuracy; and escalate issues to the Clinical Operations Manager /Study Lead as needed. +...and final reviews of study data in preparation of regulatory submissions. + May interact with RA /QA… more
    Abbott (03/15/24)
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  • Manager , Clinical Supplies

    Bausch Health (Bridgewater, NJ)
    …to the TMF as per departmental and Corporate requirements that comply with all regulatory requirements. + Participate in clinical study team meetings, align with ... study objective, and provide supporting information to the teams (includes RA , RACMC, Clinical Operations, Manufacturing and Development) **Qualifications** +… more
    Bausch Health (04/10/24)
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  • Summer Intern, Clinical Affairs

    Zimmer Biomet (Warsaw, IN)
    …recognized. **What You Can Expect** Under supervision of the Clinical Study Manager , the Clinical Affairs Intern (CAI) is responsible for administrative ... focusing on biostats, clinical research, quality systems or regulatory affairs . + GPA of 3.2+ preferred **Travel Expectations** None EOE/M/F/Vet/Disability more
    Zimmer Biomet (04/04/24)
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