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    Senior Clinical Trial Manager - San Diego, United States - EPM Scientific

    EPM Scientific
    EPM Scientific San Diego, United States

    3 weeks ago

    Default job background
    Pharmaceutical / Bio-tech
    Description

    Senior Clinical Trial Manager

    San Diego, CA (Hybrid)

    $160,000 - $180,000

    Job Description

    EPM is partnered with a trailblazing biotech nestled in sunny San Diego, dedicated to pioneering breakthroughs at the intersection of oncology and immunology. Leveraging cutting-edge research and innovative technologies, they're committed to developing targeted therapies that harness the power of the immune system to combat cancer. With a passionate team of experts and a relentless drive for innovation, they are revolutionizing cancer treatment and bringing hope to patients worldwide.

    Key Qualifications

    • Proven track record with a significant duration of experience working specifically in the field of Autoimmunity within the pharmaceutical or biotech industry.
    • In-depth knowledge of Oncology and Immunology clinical trials, including protocol design, patient recruitment, and monitoring, with a demonstrated ability to navigate the unique challenges associated with neurological disorders.
    • Comprehensive understanding of regulatory requirements and guidelines, ensuring compliance with regulatory standards throughout the drug development process.
    • Substantial experience in managing investigational sites, building and maintaining effective relationships, and optimizing site performance to ensure successful trial execution.
    • Proficiency in overseeing data review processes, including source data verification and analysis, to ensure the accuracy and integrity of clinical trial data in the autoimmune therapeutic area.

    Roles & Responsibilities

    • Lead and oversee the planning, initiation, and execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards.
    • Effectively manage relationships with investigational sites, fostering collaboration, providing support, and addressing site-specific needs to optimize site performance throughout the trial.
    • Implement robust data monitoring processes, conducting regular reviews and source data verification to ensure the accuracy and integrity of data collected in clinical trials.
    • Ensure all aspects of clinical trials comply with relevant regulatory requirements and guidelines, collaborating with regulatory affairs to address any compliance-related issues and facilitate successful trial outcomes.
    • Proactively identify potential risks associated with Oncology trials and develop strategic plans for risk mitigation. Address and resolve issues promptly to ensure the smooth progression of the trial and meet project timelines.

    Benefits

    • Medical, dental, vision insurance
    • 401(k)
    • PTO and Holidays
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