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    Senior Clinical Research Associate Medical Device REMOTE - Dallas, United States - Provident Research Inc

    Provident Research Inc
    Provident Research Inc Dallas, United States

    6 days ago

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    Description
    Job Description

    Job Description

    This Remote position located in the USA will be working with Provident Research Inc. in a dedicated Functional Source (embed) relationship.

    Our client is a major manufacturer of Medical Devices and this role is responsible for managing clinical activities at multiple study sites, as well as fostering strong, productive relationships with colleagues within the Organization.

    Interviews are being scheduled now to fill immediate openings.
    Previous Medical Device experience Mandatory.
    Responsible for managing clinical study activities for multiple sites in single or several Clinical Projects.
    Oversees performance of appointed study sites conducting company initiated clinical studies.
    Responsible for the site visits, monitoring, communication and deliverables for the assigned study sites.

    Serves as a member of the clinical study team and is the liaison between Clinical Operations and Study Site personnel for the specific clinical projects.

    This opening is immediate due to expansion.

    Benefits:
    This position affords you an opportunity to experience many different aspects of the clinical development industry. Our client is proud to offer a career pathway that looks to internal candidates for promotion.
    For the right individuals, this position offers a competitive salary along with:
    Medical, Dental, and Vision
    Disability
    Life Insurance
    401(k) Plan
    Paid Vacation and Holidays
    Education
    A Bachelor Degree is required.
    Experience

    Previous Regional monitoring required
    Requires understanding and application of regulations and standards applied in clinical research areas
    Relevant industry certifications preferred (i.e. CCRA, RAC, CDE)

    Demonstrated competencies in the following areas are required:
    Leadership
    Strong Written and Verbal Communications
    Strong organizational skills
    Ability to travel Regionally up to 65%
    Attention to details

    Key Job Activities:
    Build relationships with investigators and site staff
    Monitor patient safety on-site (review for missing SAEs, AEs, ConMed) and address protocol violations
    Take responsibility for specific tasks on projects, or acts as the main CRA contact on individual projects
    Perform on site visits in accordance with the monitoring plan
    Conduct on-site study-specific training (if applicable)
    Perform site facilities inspection
    Monitor and maintain ICH-GCP compliance
    Company Description PRI is dedicated to providing our employees with the tools to succeed. Come and join the movement

    Company Description

    PRI is dedicated to providing our employees with the tools to succeed. Come and join the movement
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