• Daiichi Sankyo, Inc. (Bernards, NJ)
    …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... as well as instruct teams on how to properly conduct high quality clinical evaluation of signals in the appropriate tool (eg, disproportionality assessments).This… more
    HireLifeScience (09/03/25)
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  • Lupin Pharmaceuticals (Coral Springs, FL)
    …field.Proven leadership abilities, strong knowledge of regulatory frameworks (eg, FDA), GCP guidelines, and quality management systems.Preferred but Not ... Mandatory: Medical practice experience in respiratory medicine.Lupin is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, gender, religion,… more
    HireLifeScience (09/15/25)
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  • Associate Director , Clinical…

    Gilead Sciences, Inc. (Foster City, CA)
    …procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director will be a key member of the Connect GCP ... team and collaborate with Clinical Operations personnel to ensure quality , proactively identify risk, mitigate non-compliance, and support deviation management… more
    Gilead Sciences, Inc. (11/06/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ... and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and … more
    Takeda Pharmaceuticals (11/14/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and … more
    Takeda Pharmaceuticals (10/14/25)
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  • Associate Director , Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director , ... Clinical Research Regulatory Job Description Summary With the oversight of the Director , the Associate Director for Regulatory Affairs will oversee the… more
    University of Pennsylvania (10/09/25)
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  • Associate Director , Quality

    Bristol Myers Squibb (Madison, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will mainly be responsible for ... developing the Quality Narrative at the study and/or ASSET and TA...regulatory compliance. **Required Competencies:** + Demonstrated applied knowledge of ICH/ GCP , regulatory guidelines/directives, clinical research processes and principles of… more
    Bristol Myers Squibb (10/30/25)
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  • Associate Director Oncology Research…

    Penn Medicine (West Chester, PA)
    …future each day. Are you living your life's work? **Summary** : + The Associate Director Oncology Research Operations reports directly to the Senior Director ... Community Impact at Penn Medicine Chester County Hospital0. The Associate Director works closely with the Physician...show vigilance in patient safety, protocol compliance and data quality . This employee must adhere to the requirements of… more
    Penn Medicine (10/14/25)
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  • Clinician/Clinical Scientist, Associate

    Pfizer (Collegeville, PA)
    …SUMMARY** + The overall role of the Early Clinical Research Clinician/Clinician Scientist Associate Director is to support the development and execution of ... of concept (PoC) studies in a given therapeutic area. + The Clinician/Clinical Scientist Associate Director may be mentored by a more senior Early Clinical… more
    Pfizer (11/12/25)
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  • Associate Director , ICSR Management…

    Ascendis Pharma (Princeton, NJ)
    …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... in the safety database and are reported according to ICH- GCP guidelines, Healthy Authority regulations and company SOPs, Work...PV Vendor processing ICSRs for Ascendis Products. + Performs Quality Checks of processed ICSRs and provides feedback to… more
    Ascendis Pharma (10/09/25)
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  • Associate Director , Clinical…

    Pfizer (Bothell, WA)
    **Job Summary** The Associate Director , Clinical Development Medical Director : + Is accountable for the medical & scientific integrity of the study and the ... clinical and medical colleagues, clinical operations, and other functional lines. The Associate Director , Clinical Development Medical Director is… more
    Pfizer (11/12/25)
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  • Associate Director , Clinical Data…

    Xeris Pharmaceuticals, Inc. (Chicago, IL)
    …outsourcing, oversight and risk-based data management strategies, standards and processes. The Associate Director , Data Management will bring deep knowledge of ... management strategies, processes, and standards in alignment with Good Clinical Practices ( GCP ) and applicable regulatory guidelines (eg, FDA, EMA, ICH). * Oversees… more
    Xeris Pharmaceuticals, Inc. (10/30/25)
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  • Associate Medical Director

    ThermoFisher Scientific (Sparks, NV)
    …includes a drug screening. Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is ... an office-based position for a motivated Physician. The Associate Medical Director serves as the physician...being conducted under all applicable laws, regulations and per ICH- GCP guidelines in the organization's Clinical Research Unit (CRU).… more
    ThermoFisher Scientific (11/15/25)
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  • Associate Director , GVP Audits

    Gilead Sciences, Inc. (Foster City, CA)
    …aspirations. Join Gilead and help create possible, together. **Job Description** The Associate Director , Good Pharmacovigilance Practice (GVP) Audits, serves as ... a key role within Gilead's R&D Quality Organization. This role is responsible for executing internal...Program. Reporting to the Head of GVP Audits, the Associate Director contributes to the strategic development… more
    Gilead Sciences, Inc. (10/24/25)
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  • Associate Director , Clinical Data…

    Bristol Myers Squibb (San Diego, CA)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Job Title:** Associate Director , Clinical Data Management **Department:** Biometrics ... Status:** Exempt **Reports to:** Director , Clinical Data Management **Summary** The Associate Director , Clinical Data Management, will play a crucial role in… more
    Bristol Myers Squibb (11/08/25)
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  • Associate Director , Data Scientist…

    J&J Family of Companies (Spring House, PA)
    …https://www.jnj.com/innovative-medicine Johnson & Johnson Innovative Medicine is currently seeking an ** Associate Director , Data Science** , to join our ... Preclinical Sciences and Translational Safety (PSTS), is seeking a highly motivated Associate Director to lead the delivery of transformative data analytics… more
    J&J Family of Companies (11/19/25)
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  • Associate Director -Clinical…

    Philips (Cambridge, MA)
    …of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations, is responsible for day-to-day Clinical ... Management and providing expertise in clinical research process legislation, ICH- GCP guidelines, improving efficiency in clinical execution. **Your role:** +… more
    Philips (11/13/25)
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  • Associate Director , DevOps…

    Humana (Denver, CO)
    **Become a part of our caring community and help us put health first** The Associate Director of DevOps Engineering is a strategic and technical leadership role ... of continuous improvement and collaboration across engineering and operations teams. The Associate Director of DevOps will bring in industry best-practices,… more
    Humana (10/21/25)
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  • Sr. Associate Director

    Boehringer Ingelheim (Ridgefield, CT)
    …and Metabolism (ExpMed - CRM) is currently seeking a talented and innovative Senior Associate Director , Clinical Trial Leader to support our ExpMed team to join ... field from start of development (SoD) to proof of concept (PoC). The (Senior) Associate Director , Clinical Trial Leader (AD, CTL) is accountable for the set-up,… more
    Boehringer Ingelheim (11/12/25)
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  • Associate Clinical Project Management…

    IQVIA (Boston, MA)
    **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate global ... and interfacing with internal and external stakeholders to ensure compliance, quality , and timely delivery of trial milestones. **Key Responsibilities:** **Trial… more
    IQVIA (10/22/25)
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