Clinical Trial Associate

Allen Spolden
  • New Brunswick, New Jersey
    30+ days ago

    Job Description

    The remote-based Clinical Trial Associate (CTA) will perform tasks related to supporting operational strategy and and execution of clinical studies, supporting the strategy as defined in the Clinical Development Plan.

    • Provide support for essential daily clinical study activities, including regulatory inspection readiness, following established protocols under the general management of the CTA Manager.

    • Work with Clinical Operations Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model.

    • Perform departmental tasks.

    • Perform developmental tasks with oversight of CTA Manager.

    ACCOUNTABILITIES:


    For assigned complex, accelerated, and business essential studies, provide support to focus on study startup and site initiation activities, including:

    • Approval of study documentation, including essential document packets, study plans, informed consent forms, etc.

    • Support oversight of risk-based monitoring.

    • Attend important team meetings.

    • Support regulatory inspection readiness (e.g. preparation of materials and participation during regulatory inspections.)

    • Support additional ad-hoc activities, as agreed with CTA Manager.

    • Work with internal departments (Legal, Insurance, R&D functions), CROs, and vendors.

    • Escalate clinical trial insurance issues.

    • Support Health Care Provider Engagement for facilitating contracts and meetings.

    • Support vendor contract administration.




    Requirements

    • Bachelor's degree or equivalent international degree.

    • 1 or more years' experience in pharmaceutical industry, clinical research organization, or related role.

    • Experience in Phase 2 and 3 studies and global/international studies is advantageous.

    • Experience working across multiple therapeutic areas is advantageous.

    • Knowledge in global regulatory and compliance requirements for clinical research.

    • Excellence in task management and collaboration.

    • Requires availability for 5-10% domestic and international travel, including overnight and international travel on an as-needed basis.



    Benefits

    • 401(k) with company match and Annual Retirement Contribution Plan

    • Tuition reimbursement Company match of charitable contributions

    • Health & Wellness programs including onsite flu shots and health screenings

    • Generous time off for vacation and the option to purchase additional vacation days

    • Community Outreach Programs



    Numbers & Facts

    LocationNew Brunswick, New Jersey
    Websitewww.allenspolden.com

    Skills

    • Administrative Skillsunmatched
    • Biotech and Pharmaceuticalunmatched
    • Clinical Researchunmatched
    • Clinical Supportunmatched
    • Clinical Trialunmatched
    • Community Programsunmatched
    • Contract Managementunmatched
    • Contract Research Organization (CRO)unmatched
    • Drug Developmentunmatched
    • Healthcare Providersunmatched
    • Insuranceunmatched
    • Legalunmatched
    • Operational Strategyunmatched
    • Operational Supportunmatched
    • Operations Managementunmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Research & Development (R&D)unmatched
    • Risk Managementunmatched
    • Site Initiationunmatched
    • Startupunmatched
    • Willing to Travelunmatched

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