• Director , Regulatory Medical

    J&J Family of Companies (Spring House, PA)
    Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory ... people can reach their potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a highly experienced … more
    J&J Family of Companies (11/07/24)
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  • Associate Director , CMC Regulatory

    J&J Family of Companies (Spring House, PA)
    Associate Director , CMC Regulatory Affairs - 2406221330W **Description** Johnson & Johnson is recruiting for an Associate Director , CMC Regulatory ... Authorities. + Provides technical expertise and technical input in the preparation and writing (as applicable) of regulatory dossiers for submission to Health… more
    J&J Family of Companies (11/07/24)
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  • Director , Translational Medicine and Early…

    Organon & Co. (Plymouth Meeting, PA)
    …support the approved early development plans. The TMED Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction ... **The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible for… more
    Organon & Co. (10/17/24)
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  • Director of Health Justice Transformation…

    Penn Medicine (Philadelphia, PA)
    …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... Blvd. Philadelphia, PA** **Hours: 8hr Days (HYBRID)** **Summary** : + **The Director of Health Justice Transformation** is a unique opportunity to help establish… more
    Penn Medicine (10/17/24)
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  • Senior Director Clinical Development…

    Teva Pharmaceuticals (West Chester, PA)
    …results and provide a guidance to prepare high quality reports working with Medical Writing + Responsible for authoring protocol synopses and working with ... (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director will provide... Medical Affairs and provides input and direction to the… more
    Teva Pharmaceuticals (10/03/24)
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  • Director , Scientific Communication, Global…

    Olympus Corporation of the Americas (Center Valley, PA)
    …**__** Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can ... other than @Olympus.com, it is likely not legitimate._ **Job Description** The Director Scientific Communications, Global Operations plays a central role in the… more
    Olympus Corporation of the Americas (10/17/24)
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  • Research Project Director

    University of Pennsylvania (Philadelphia, PA)
    …wellness programs and resources, and much more. Posted Job Title Research Project Director Job Profile Title Manager Research Project C Job Description Summary The ... phenomena at both the basic and applied levels. The Lab is led by Director Dolores Albarracin, Ph.D., the Alexandra Heyman Nash University Professor, and the 28th… more
    University of Pennsylvania (10/03/24)
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  • Associate Director , Clinical Scientist…

    Merck (North Wales, PA)
    …lead clinical scientist on the clinical trial team. + Collaborates with the Medical Writer on clinical/scientific and regulatory documents. + Partners with Study ... of clinical data/ medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities of direct and indirect team members… more
    Merck (11/05/24)
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  • Assistant Activities Director

    Genesis Healthcare (Wayne, PA)
    …pay classification, job grade, location, and length of service. The Assistant Recreation Director is responsible for assisting the Recreation Director in the ... to the development of program philosophies and policies, along with writing procedures, goals and objectives for the program.*Contribute to the implementation… more
    Genesis Healthcare (09/04/24)
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  • Executive Director , Group Head,…

    Organon & Co. (Plymouth Meeting, PA)
    …promotional regulatory strategy in collaboration with Commercial, PRT, Global Regulatory Liaisons, Medical Affairs and Worldwide Product Labeling. + Guide ... writing ability, effective communication and familiarity with worldwide regulatory agencies. + Experienced in negotiations with health authorities. + Outstanding… more
    Organon & Co. (10/23/24)
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  • Manager, Regulatory Promotional Operations

    Publicis Groupe (Philadelphia, PA)
    …and career development + Provide estimates for SOW development + Work with the Director , Regulatory Review in the development of departmental SOPs + Oversee work ... www.digitashealth.com | Facebook: www.facebook.com/digitashealth| Twitter: www.twitter.com/digitas_health **Overview** The Manager, Regulatory Review is responsible for managing a team of… more
    Publicis Groupe (11/05/24)
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  • Senior Scientific Advisor, Publications,…

    IQVIA (Wayne, PA)
    …Publications, Medical & Scientific Communications** **Agency Equivalent: Senior Scientific Director , Publications** In concert with the medical leads, the ... crafting a strategically relevant poster for a congress, or writing a target journal outreach email, this candidate will...Advisor will interface with all stakeholders, from clients to medical leads, senior management to medical writers,… more
    IQVIA (10/11/24)
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  • Nonclinical Submissions Writer, Preclinical…

    J&J Family of Companies (Spring House, PA)
    …such as nonclinical safety, pharmacokinetic, and discovery biology project leaders, medical writers, global regulatory dossier leaders, and other subject ... Skills:** **Required:** + Experience working globally as lead author on writing Toxicology, Pharmacology, Pharmacokinetics, or Bioanalytical regulatory documents… more
    J&J Family of Companies (11/09/24)
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  • Oncology Late

    Pfizer (Collegeville, PA)
    …study team in governance meetings and submissions, partners with/supports the Development lead/ Medical Director regarding study and disease area strategy. + ... **ROLE SUMMARY** The Late-Stage Clinical Scientist (non-MD, Director ) is responsible for scientific oversight, data integrity and quality of clinical trial(s) in… more
    Pfizer (10/23/24)
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  • Myeloma Research Program Manager (Cancer Center)

    University of Pennsylvania (Philadelphia, PA)
    …Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work closely with ... of the team's work, working closely with the CRU Regulatory coordinators to manage, review and initiate trials to...The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's, report… more
    University of Pennsylvania (10/27/24)
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  • Supervising Intake Attorney

    Community Legal Services, Inc. (Philadelphia, PA)
    …will also involve collaboratively working with the Managing Attorney of Intake, Deputy Director of Legal Practice, the Director of Law and Technology, Legal ... data and metrics regarding intake and reporting to the Managing Attorney and Deputy Director of Legal Practice. + Assisting the management team in leading change and… more
    Community Legal Services, Inc. (09/06/24)
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  • Clinical Research Project Manager A/B (Abramson…

    University of Pennsylvania (Philadelphia, PA)
    …personnel in the biospecimen process, shipping and inventory to ensure all regulatory , institutional and PAH CRU policies and procedures is followed. This position ... in the development of investigator-initiated trials and have responsibilities in writing the protocol, database creation, data collection sheets, anaylsis and… more
    University of Pennsylvania (11/01/24)
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  • Sterilization Manager - Validation, Sterility…

    PCI Pharma Services (Philadelphia, PA)
    …Utilities/Facilities** Department/Group: Quality / Validation Location: Philadelphia Reports to: Director , Validation FLSA Status: Exempt Prepared By: Dennis Gerlach ... the site commercial Validation Manager for any validation overlap. Assures regulatory and any applicable customer requirements are accurately incorporated into PCI… more
    PCI Pharma Services (10/29/24)
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  • Manager, Research Project B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …will also be responsible for engaging with the Institutional Review Board (IRB), regulatory affairs, and the Office of Clinical Research to generate documents for AE ... capacity. The project manager reports to the Penn FTDC Director (Irwin) and works closely with associated faculty in...responsible for engaging with the Institutional Review Board (IRB), regulatory affairs, and the Office of Clinical Research to… more
    University of Pennsylvania (10/27/24)
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  • Clinical Research Nurse C/D (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …is currently comprised of 12 Research Teams that support disease/discipline specific medical oncology cancer programs within the ACC. The Cell Therapy & Transplant ... products and various sponsors. This position will report directly to the Director of Clinical Research Operations and work directly with Physician Investigators… more
    University of Pennsylvania (10/27/24)
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