Clinical Research Associate I — In-House

Worldwide Clinical Trials; Barcelona; On-site; EUR 45,000 - 65,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager to drive data quality and regulatory submissions across multiple study sites. You will coordinate with site personnel to ensure timely data reporting and maintain TMF documentation in a collaborative, global CRO environment.

You will work with cross-functional teams to support feasibility studies and site identification, contributing to ongoing clinical trial excellence and patient outcomes.

Responsibilities

• Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel
• Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.)
• Provide applicable updates for site related documentation for filing in the Trial Master File (TMF)
• Perform feasibility studies/site identification activities for potential sites, as requested

Job description

Worldwide Clinical Trials is seeking a Clinical Operations Site Manager to drive data quality and regulatory submissions across multiple study sites. You will coordinate with site personnel to ensure timely data reporting and maintain TMF documentation in a collaborative, global CRO environment.

You will work with cross-functional teams to support feasibility studies and site identification, contributing to ongoing clinical trial excellence and patient outcomes.