• Associate Director, Regulatory

    University of Pennsylvania (Philadelphia, PA)
    Associate Director for Regulatory Affairs will facilitate ongoing improvement of clinical trial compliance and quality assurance through communication of ... with IND/IDE/Expanded Access Applications, drug development process, medical writing, and clinical trial operations required. + Qualified candidates must also… more
    University of Pennsylvania (10/09/25)
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  • Associate Principal Statistical Programmer,…

    Merck (North Wales, PA)
    …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment MS in Computer Science, Statistics, Applied Mathematics, ... all our company therapeutic areas except early oncology. The Associate Principal Programmer will gather and interpret user requirements...7 or more years SAS programming experience in a clinical trial environment Department Required Skills and… more
    Merck (11/19/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …Engineering or related field plus 9 years SAS programming experience in a clinical trial environment. + MS in Computer Science, Statistics, Applied Mathematics, ... 7 or more years SAS programming experience in a clinical trial environment. **Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, Monday - Thursday, although the specific… more
    Merck (09/30/25)
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  • Principal Scientist, Clinical Research,…

    Merck (Upper Gwynedd, PA)
    … Development, Clinical Immunology, Clinical Investigations, Clinical Medicine, Clinical Research, Clinical Trial Planning, Clinical Trials, ... clinical development projects + Assist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in ensuring that… more
    Merck (11/22/25)
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  • Associate Director, Biostatistics

    Pfizer (Collegeville, PA)
    …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... the reporting of clinical trial results to regulatory authorities and...dental and vision coverage. Learn more at Pfizer Candidate Site - US Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures… more
    Pfizer (11/19/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Harrisburg, PA)
    …in Lupus is preferred *Experienced as a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability ... experience treating rheumatology patients clinically and/or who possess extensive rheumatology clinical trial related experience will be considered for this… more
    Parexel (10/11/25)
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  • CRA 2, Early Clinical Development, IQVIA…

    IQVIA (Philadelphia, PA)
    …candidates located East, Central or West Coast. **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and play a key ... IQVIA Early Clinical Development is hiring for CRA 2. Ideal...essential documents are collected and maintained in both the Trial Master File (TMF) and the Investigator Site more
    IQVIA (11/01/25)
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  • Associate Director, RWE Statistics

    Teva Pharmaceuticals (West Chester, PA)
    …* Expertise with multiple RWD sources (eg, EHR, claims, registry data); familiarity with clinical trial design. * Proficiency in programming skills in SAS, R, ... Associate Director, RWE Statistics Date: Oct 30, 2025...presentations in RWE methods is preferred. * Familiarity with clinical trial data standards (ADaM/SDTM) and data… more
    Teva Pharmaceuticals (10/02/25)
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  • CRA II/Senior CRA

    ICON Clinical Research (Blue Bell, PA)
    …as a Clinical Research Associate , with a strong understanding of clinical trial processes and regulatory requirements. + Located in the Central, West or ... clinical development. We are currently seeking a **Senior Clinical Research Associate (CRA)** to join our...and site management, with proficiency in relevant clinical trial software and tools. + Excellent… more
    ICON Clinical Research (10/08/25)
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  • Quality Assurance Document Control…

    Catalent Pharma Solutions (Philadelphia, PA)
    …and approve batch records before production to ensure compliance with cGMP, clinical trial protocols, and blinding requirements. + Monitor production schedules ... Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated… more
    Catalent Pharma Solutions (11/05/25)
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