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Sr In-House CRA (Warsaw IN or Raynham MA)

Company: Kelly Services
Location: Raynham
Posted on: April 9, 2021

Job Description:

SR In-House CRA Kelly Services is currently seeking a Sr In-House CRA for a long-term engagement with one of our Global Pharmaceutical clients in Warsaw IN or Raynham MA . This role will be remote working at home until Covid restrictions are lifted with ability to come into the site when requested. ----This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vison, 401K, and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.This individual will be responsible for supporting and managing one or more clinical trials within the Clinical R&D Operations, as well as fostering strong, productive relationships with colleagues across the organization. Serves as the trial leader for clinical study executionRESPONSIBILITIES:

  • Serve as a Senior Clinical Research Associate within the Clinical R&D Operations CoE operations group to execute company sponsored clinical trials for the Medical Device Franchises
  • Manage all operational activities of assigned clinical studies within the Clinical R&D Operations group
  • Serves as a member of the clinical trial/study core team and may serve as the liaison with the Clinical R&D Franchise and Clinical R&D BSDM for projects under his/her responsibility
  • May serve as the primary contact for clinical trial sites
  • Solves problems with support from Clinical Management arising during clinical study execution, and will seek guidance for more complex problems, as needed
  • Provide internal communication of important clinical data and events. Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
  • May be involved in other tasks to support Clinical R&D Operations and R&D Clinical Franchise as needed
  • Track assigned projects budgets to ensure adherence to business plans
  • Support the implementation of new clinical systems/processes, and provide support for publications, as needed.
  • Interface and collaborate with site personnel, IRBs/ECs, Competent Authorities/MoH, contractors/vendors, and company personnel
  • Ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety, and Environmental compliancePeople Leadership Responsibilities:
    • Provide direction within a clinical trial, ensuring that each team member has a well-defined set of activities and objectives specific to their role and responsibilities within the context of their business focus.
    • Ensure efficient use of resources within the clinical study/program to provide high quality deliverables.Business Leadership Responsibilities:
      • Accountable for quality, compliance with regulations and company procedures, timelines, and budgets for assigned clinical trials.
      • May support or lead several small/medium clinical trials (regulated and non-regulated) and/or a small number of large non-regulated projects that may involve other clinical operations staff (i.e., > 250K USD annual investment).
      • May assist with the management of large regulated or complex trials/program under supervision of CTM or Senior CTM.
      • Identify and ensure strategies, resources, and accountabilities are in place to achieve rapid, high quality execution of assigned clinical trials under his/her responsibilities.
      • Reviews and provides feedback on clinical operation section of protocols with supervision.
      • May plan budgets for single trials with supervisionQUALIFICATIONS:----------------------
        • BS degree with at least 4 years relevant experience preferred.
        • Previous experience in clinical trial management or equivalent is required
        • Clinical/medical background a plus
        • Medical device experience a plus
        • Experience managing study deliverables on allocated studies and those of any in-direct or direct reports are met on time, and within budget and in compliance to SOPs and regulationsWhy Kelly--?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.About Kelly--At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world. Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.]]

Keywords: Kelly Services, Brockton , Sr In-House CRA (Warsaw IN or Raynham MA), Other , Raynham, Massachusetts

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