• Senior Clinical Trials Manager

    Job Locations US-MD-Silver Spring
    # of Openings
    1
    Category
    Medical Research
    Type
    Regular Full-Time
  • Overview

    CAMRIS International is a medical research and development firm that realizes innovative solutions to health and development challenges through high-quality, cost-effective program and research management services. We combine our proven systems with today’s most effective, evidence-based best practices to improve the lives of people around the world. Our core practice areas include HIV/AIDS, microbiology and infectious disease research, vaccine research, development and production, global health security, biodefense, and clinical research.

     

    CAMRIS is seeking a Senior Clinical Trials Manager who will be responsible for clinical trial support services at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland. 

    Responsibilities

    • As a CTM you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. 
    • Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
    • Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
    • Contribute to the development and maintenance of cross functional project management plans
    • Responsible for risk mitigation strategies, associated action plan and issue resolution
    • Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
    • Provide direction and support to the Clinical Operations study team
    • Track Clinical Operations project deliverables using appropriate tools 

    Qualifications

    • Must have experience in Infectious Diseases, and/or Vaccines trials.
    • Must have previous experience in a Clinical Trial Manager role. 
    • University/Bachelor’s Degree in Medicine or Life Sciences.
    • A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities 
    • Previous working experience within the clinical trial management field.
    • Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
    • Some knowledge of project management processes and tools.
    • Managerial and personnel experience.
    • Fluent in written and spoken English.  
    • Proficient in Microsoft Office.
    • Registered Nurse, Clinical Research Coordinator or Clinical Research Administrator

     Security Requirements

    • All proposed personnel to perform services contractor must verify employment eligibility (E-Verify) and also obtain a favorable National Agency Check (NACI).

    Options

    Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
    Share on your newsfeed