Research Study Coordinator

4 days ago


Oslo, Oslo County, Norway IQVIA Argentina Full time
Responsibilities

The Research Study Coordinator will be responsible for coordinating and managing the logistics of clinical trials conducted at research sites. This includes collaborating with sites to develop and implement strategies to enhance subject recruitment and retention, administering protocol and related study training to assigned sites, and establishing regular lines of communication to manage ongoing project expectations and issues.

Key Responsibilities:

  1. Collaborate with sites to develop and implement strategies to enhance subject recruitment and retention.
  2. Administer protocol and related study training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues.
  3. Evaluate the quality and integrity of study site practices and escalate quality issues as necessary.
  4. Ensure that 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 GCP and local regulatory requirements.
  5. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution.
  6. Collaborate and liaise with study team members for project execution support as necessary.
  7. If applicable, may be accountable for supporting development of project subject recruitment plans on a per-site basis.
  8. If applicable, may be accountable for site financial management according to executed clinical trial agreements and retrieving invoices according to local requirements.


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