• Statistics & Data Corporation (SDC) (Waltham, MA)
    …analysis plan as well as any post-hoc analyses and relevant exploratory analyses of clinical trial data *Prepare/review key sections of clinical ... specialized contract research organization (CRO) headquartered in Arizona, delivering top-tier clinical trial services to pharmaceutical, biologic, and medical… more
    Upward (08/04/25)
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  • Data Integrity / Clinical

    Dana-Farber Cancer Institute (Brookline, MA)
    The Data Integrity / Clinical Trials Billing Specialist performs charge validation through account review in a timely and billing compliant manner. The ... Data Integrity / Clinical Trials Billing Specialist will develop a mastery of the Institute's Accounts Receivable (AR) and Clinical Trials Management… more
    Dana-Farber Cancer Institute (09/09/25)
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  • Clinical Research Project Manager - Head…

    Dana-Farber Cancer Institute (Boston, MA)
    …based on PI directives and maintains study-related databases, ensuring data integrity and compliance with clinical trial standards. Prepare ... coordination and management of Head & Neck Oncology (HNO) clinical trial activities, primarily focusing on multi-center,...and tools, such as EPIC and OnCore, for efficient trial coordination. + Awareness of data management… more
    Dana-Farber Cancer Institute (09/11/25)
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  • Clinical Trial Physician,…

    Bristol Myers Squibb (Cambridge, MA)
    …may be a member of the Clinical Development Team (CDT) + Conducts medical data review of trial data , including eligibility review + Holds responsibility ... personal lives. Read more: careers.bms.com/working-with-us . **Functional Area Description** The Clinical Trial Physician sits within Clinical Development,… more
    Bristol Myers Squibb (10/02/25)
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  • Manager, Clinical Trials Registry

    Dana-Farber Cancer Institute (Brookline, MA)
    …investigators, research teams, and regulatory staff to maintain the integrity of clinical trial data and ensure timely submissions to registries such ... trials registry. Reporting to the Director, Office of Data Quality, in the department of Clinical ...+ Provide training and guidance to research staff on clinical trial registration requirements, submission processes, and… more
    Dana-Farber Cancer Institute (09/06/25)
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  • Manager, Global Clinical Compliance

    J&J Family of Companies (Danvers, MA)
    …European General Data Protection Regulation (GDPR) required + Knowledge of clinical trial applications, including prior knowledge and experience with Veeva ... more at https://www.jnj.com **Job Function:** R&D Operations **Job Sub** **Function:** Clinical Trial Project Management **Job Category:** Professional **All Job… more
    J&J Family of Companies (10/08/25)
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  • Senior Director, Global Clinical

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …optimize the scientific integrity of the methodology and ensure the safety of clinical subjects. + Leading clinical trial projects to ensure all aspects ... of the clinical trial project plan (eg, enrollment, database lock) are achieved...Requires thorough knowledge of clinical medicine and/or clinical pharmacology and associated disciplines (eg biostatistics, data more
    Otsuka America Pharmaceutical Inc. (10/14/25)
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  • Lead Clinical Programmer- FSP

    Parexel (Boston, MA)
    …and logistics. * Lead cross-functional study teams, manage vendor relationships, and oversee clinical trial biosamples and data monitoring. * Oversee and ... departmental goals. * Oversee operations, including samples, kits, and data processes, ensuring integrity and completeness for...manage clinical trial biosamples and data monitoring and completeness… more
    Parexel (10/11/25)
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  • Associate Medical Director/Medical Director,…

    AbbVie (Cambridge, MA)
    …Participates in cross-functional teams to generate, deliver, and interpret high-quality clinical data supporting overall product scientific and business ... supervision. + Strong desire to collaborate in a cross-functional setting. + Clinical trial experience in the pharmaceutical industry, academia, or equivalent… more
    AbbVie (09/26/25)
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  • Associate Director, Neuroscience, Clinical

    Bristol Myers Squibb (Cambridge, MA)
    …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial /biomarkers and asset development as well as ... in late stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written… more
    Bristol Myers Squibb (10/12/25)
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  • Senior Medical Director, Clinical Science,…

    Takeda Pharmaceuticals (Cambridge, MA)
    …Director leads and drives strategy for the overall global (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and ... the input from various disciplines to create, maintain, and execute a global clinical development plan that will result in the regulatory approval of the assigned… more
    Takeda Pharmaceuticals (10/09/25)
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  • Clinical Project Manager

    Massachusetts Institute of Technology (Cambridge, MA)
    …stakeholders and study sites; oversee day-to-day operations of ongoing research and clinical trial projects; identify and resolve bottlenecks or delays; ensure ... Clinical Project Manager + Job Number: 25043 +...of decisions and communications across projects; support recruitment goals, data integrity and patient visit coordination as… more
    Massachusetts Institute of Technology (10/02/25)
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  • Vice President, Global Program Lead Neuroscience

    Bristol Myers Squibb (Cambridge, MA)
    …plan, incl., clinical plans and labeling strategy; Appreciates translation of clinical data into claims and considerations for label development + ... positioning, messaging, campaign, segmentation, promotional strategy) understanding the relationship to clinical trial design + In partnership with Medical… more
    Bristol Myers Squibb (08/29/25)
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  • R & D Patient Engagement Country Lead

    Sanofi Group (Cambridge, MA)
    …strategies. This position extends beyond the classical patient insights generation and clinical trial operations activities by having direct accountability for ... Development Plan, the Integrated Patient Journey (IPJ) and the clinical trial designs is core to ensuring...be evidenced because of the collaboration (eg Patient Experience Data (PED) utilized to optimize study design, PED integrated… more
    Sanofi Group (10/08/25)
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  • AI Solution Architect

    Norstella (Boston, MA)
    …by applying leading AI and Data Science enabled solutions across the clinical trial planning, feasibility, and recruitment space, helping clients meet their ... Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug...expertise to a team in accelerating AI solutions across clinical trial strategy, planning and execution. This… more
    Norstella (08/08/25)
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  • Executive Medical Director - Cardio-Renal

    Lilly (Boston, MA)
    …of external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... plans with business unit and LRL priorities. + Understand and keep updated with the pre- clinical and clinical data relevant to molecules + Represent Lilly in… more
    Lilly (09/06/25)
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  • Associate Director, Patient-Centered Outcomes…

    AbbVie (Waltham, MA)
    …analysis plans and reports + Leads integration of COA measurement strategy into clinical development programs through clinical trial program support (eg, ... / knowledge of the pharmaceutical industry (knowledge of regulatory/compliance frameworks) and clinical trial design + Knowledge of regulatory & HTA requirements… more
    AbbVie (09/17/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Boston, MA)
    …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, Car-T, Iqvia Biotech

    IQVIA (Boston, MA)
    …Your work will directly contribute to the integrity and quality of clinical research data . **Key Responsibilities** + Conduct all types of site ... patients faster._ **Job Overview** We are seeking a dedicated Clinical Research Associate (CRA) to join our team and...escalating quality concerns as needed to ensure compliance and data integrity . + Monitor study progress by… more
    IQVIA (10/02/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Boston, MA)
    …regulatory submissions and working with regulatory templates + Understanding of EU Clinical Trial Regulation and ROW country regulatory requirements related to ... clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/ data ) and contributes… more
    Sumitomo Pharma (10/11/25)
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