Clinical Research Associate

Riyadh, Saudi Arabia

Job Description

Job Profile Summary Engage in structured training program to gain knowledge and skills required to
independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Essential Functions

  • Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
  • Gain experience in study procedures by working with experienced clinical staff.
  • Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with
contracted scope of work and good clinical practices.
  • Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of
communication with sites to manage ongoing project expectations and issues.
  • Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol
and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment,
Case Report Form (CRF) completion and submission, and data query generation and resolution.
  • Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File
(TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) /
International Conference on Harmonization (ICH) and local regulatory requirements.
  • Under close supervision may support start-up phase.
  • Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings
and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.
  • If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest
ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site
recruitment progress. Required Background:
  • Bachelor's Degree Degree in scientific discipline or health care preferred.
  • Equivalent combination of education, training and experience may be accepted in lieu of degree.
  • Prior clinical experience preferred.
  • 2 years of clinical experience.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

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Job Detail

  • Job Id
    JD1407155
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Riyadh, Saudi Arabia
  • Education
    Not mentioned