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    Clinical Trials Project Manager Ii - Remote

    Cpc Clinical Research
    5+ years
    $72,000 to $90,000 per year
    Remote, USA
    10 Nov. 14, 2024
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Opportunity: Clinical Trials Project Manager II at CPC Clinical Research

    Are you a highly organized professional who can adapt to unexpected changes and keep a strong focus on both the big picture and day-to-day tasks? If so, we have an exciting opportunity for you!

    We are looking for a Clinical Trials Project Manager II to join our team at CPC Clinical Research. In this role, you will be the primary point of contact for industry-sponsored clinical trials and Endpoint and Specialty Services activities.

    Responsibilities:

    • Oversee clinical operations management activities.
    • Define and monitor project scope, timelines, and deliverables from initiation to close-out.
    • Identify project-specific training for team members and ensure timely completion and filing of training documentation.
    • Oversee trial-related activities and vendor payments.
    • Provide expert advice in the design, writing, and review of project-related essential documents.
    • Develop and manage multidisciplinary project team members, ensuring overall quality of project services and deliverables.
    • Provide necessary updates and reports to the sponsor as per the contract.
    • Plan and execute investigator meetings as contracted.
    • Collaborate with the Business Development team on budgets, proposals, and change orders.
    • Ensure adherence to regulations and CPC policies, SOPs, and Work Instructions.
    • Manage and conduct Endpoint and Specialty Services CPC Core Lab activities and provide operational support for biostatistics and programming deliverables.

    Required Qualifications:

    • Nursing or BA/BS in a scientific field (or equivalent knowledge/experience).
    • Minimum of 4 years of experience in clinical research, including 2 years of project/operations management experience.
    • Strong knowledge of Good Clinical Practice guidelines and applicable FDA and ICH regulations.
    • Proficiency in Microsoft Office (Outlook, Word, Excel).
    • Excellent communication, organizational skills, and attention to detail.
    • Ability to lead multi-disciplinary teams and manage conflicts effectively.
    • Willingness to travel 20-25%.

    Compensation & Benefits:

    • Targeted Compensation: $72,000 – $90,000 annually.
    • Comprehensive benefits package including medical, dental, vision, life insurance, and more.
    • Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately).
    • Paid holidays and vacation days (15-25 days based on years of service).
    • Flexible and remote work schedules available for certain positions.

    About CPC:

    CPC is an academic research organization with over 30 years of experience in clinical trial design, oversight, and management. We focus on a variety of therapeutic areas, including cardiovascular, wound healing, diabetes, and more. CPC also offers innovative community health programs and is dedicated to helping individuals become active, empowered, and healthy.

    CPC is an Equal Opportunity Employer and encourages applicants from diverse backgrounds to apply.

    Apply directly at CPC Clinical Research Careers.

    For any assistance, please email our HR team at careers@cpcmed.org.

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