• Associate Operations Specialist

    Charles River Laboratories (Cambridge, MA)
    …laboratory procedures in compliance with established protocols/plans and with regulatory and laboratory requirements. + Document experimental data in technical ... data patterns. + Record, prepare, and analyze data for inclusion in project reports. + With guidance from scientific management, maintain technical knowledge and… more
    Charles River Laboratories (10/17/25)
    - Related Jobs
  • Sr. Manager, Strategic Sourcing

    Rhythm Pharmaceuticals (Boston, MA)
    …this individual will assist with the sourcing of goods and services for our clinical research function, work to improve the sourcing experience, and implement ... with vendors around company needs across multiple disciplines including Clinical , Regulatory , and IT. + Participate in...+ 6+ years' experience (minimum of 3 years supporting clinical operations sourcing, procurement, project management or… more
    Rhythm Pharmaceuticals (08/15/25)
    - Related Jobs
  • AI Solution Architect

    Norstella (Boston, MA)
    …Citeline is one of the world's leading providers of data and intelligence on clinical trials, drug treatments, medical devices and what's new in the regulatory ... from over 3000 of the world's leading pharmaceutical, contract research organizations (CROs), medical technology, biotechnology and healthcare service providers,… more
    Norstella (08/08/25)
    - Related Jobs
  • Electrical Engineering Manager, Robotics

    J&J Family of Companies (Boston, MA)
    …as defined in the signature matrix. + Partners with affiliated disciplines such as regulatory affairs and clinical affairs to assure adequate design inputs are ... help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions… more
    J&J Family of Companies (10/23/25)
    - Related Jobs
  • Advisor - Stem Cell Engineering and Cell Line…

    Lilly (Boston, MA)
    …work effectively in a team-oriented environment. + Proven track record of successful project management and meeting deadlines in a research setting. + Hands-on ... (NGS). + Execution of genome editing of iPSC in GMP facilities to create clinical cell lines. + Evaluate and design mitigating mechanisms to ensure genomic stability… more
    Lilly (10/14/25)
    - Related Jobs
  • Director, Thought Leader Liaison - Oncology

    Sumitomo Pharma (Boston, MA)
    …diverse pipeline of early- to late-stage assets, we aim to accelerate discovery, research , and development to bring novel therapies to patients sooner. For more ... created for KOL engagement are compliant from a legal, medical and regulatory perspective through the Promotional Review Committee (PRC) process. + Provide timely… more
    Sumitomo Pharma (10/04/25)
    - Related Jobs
  • Director of Child Life

    Children's Hospital Boston (Boston, MA)
    …Hospital. 2. Principal investigator, 60+ funds over $3 million, coordinate and project funding allocations for staff salaries and materials needed, current and ... environment which fosters excellence, sensitivity and leadership. 4. Complies with regulatory standards, laws and requirements of requisite agencies with appropriate… more
    Children's Hospital Boston (08/11/25)
    - Related Jobs
  • Director, Global Program Management, Neuroscience…

    Takeda Pharmaceuticals (Boston, MA)
    …with significant experience within related functions (eg Clinical Science, Clinical Operations, Research , Regulatory , CMC, Marketing) * Minimum ... improvements with significant organizational impact and manages, as needed, non- project responsibilities, which can include processes and system optimizations. You… more
    Takeda Pharmaceuticals (10/14/25)
    - Related Jobs
  • Senior Director, Global Program Management

    Takeda Pharmaceuticals (Boston, MA)
    …development with significant experience within related functions (eg Clinical Science, Clinical Operations, Research , Regulatory , CMC, Marketing) + 10+ ... that are represented on the GPT. + Demonstrates the ability to bring project teams to consensus, acknowledging both risks and benefits, while cultivating a culture… more
    Takeda Pharmaceuticals (10/11/25)
    - Related Jobs
  • Global Patient Access Strategy Lead

    Takeda Pharmaceuticals (Boston, MA)
    …MS with ~8+ years; BS with ~10+ years experience or related experience in clinical research or pre-approval access in the pharmaceutical industry or CRO ... strategies related to Patient Access + Serve as a main point-of-contact with project and functional teams regarding Patient Access programs and report progress on… more
    Takeda Pharmaceuticals (10/02/25)
    - Related Jobs