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CRA 2 in Providence, RI at Johnson Service Group

Date Posted: 11/8/2018

Job Snapshot

Job Description

JobID: 357955

OVERVIEW

  • Assist in planning, designing, and executing clinical studies.
  • Monitor multiple clinical trial sites and studies.
  • Ensure the overall quality of clinical trials by monitoring study data and managing site adherence to the protocol, GCP, all applicable regulations and related study documents.
  • Serve as primary contact with the study site and serve as the liaison between clinical investigators and Client.
  • Responsible for site training, regulatory document collection, tracking enrollment, and ensuring case report forms are accurate, complete and verifiable against source documents.
  • Ensure that clinical tasks are being performed in accordance with the study protocol, Client procedures, ICH-GCP Guidelines, and all applicable regulatory requirements.
  • Monitor investigative sites on as needed basis.
  • Contribute to the overall development and improvement of company procedures, processes, and templates in support of Client’s efforts towards continuous quality improvement. 
  • Work with confidential patient and company data and interfaces with a variety of internal and external customers.

REQUIREMENTS

  • 3+ years related medical device / pharmaceutical field monitoring required.
  • Ability and willingness to travel up to 75%.
  • Thorough understanding of operational aspects of clinical research and regulatory requirements.
  • Excellent interpersonal, problem solving and communication skills.
  • Excellent follow-through capability.
  • BS / BA in a related scientific or clinical field required
    • Masters Degree a plus
  • Self-motivated, attention to detail and organizational skills.
  • Demonstrable experience with various computer systems/applications and clinical trial management systems.
    • Willingness to learn new systems / databases.