Lead Clinical Trial Site Manager

Worldwide Clinical Trials S.R.L.; Argentina; Remote; ARS 1,200,000 - 1,800,000; Full time

Job summary

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site management activities across a geographic region, ensuring protocol compliance and timely delivery of study milestones.

You will supervise site qualification, initiation, monitoring and close-out, provide training to CRAs, and collaborate with project management to optimize recruitment and data quality. Travel required; a four-year degree and CRA experience are expected.

Qualifications

• Four-year college degree in biological, physical or health studies with minimum CRA experience.
• Experience as Senior Clinical Research Associate or equivalent roles.
• Strong understanding of regulatory requirements and SOPs.

Responsibilities

• Lead delivery of clinical study site management activities by coordinating a team of Clinical staff within a geographic region.
• Ensure site qualification, initiation, interim monitoring, and close-out activities per protocol and SOPs.
• Maintain overall quality and timeliness of clinical deliverables for assigned programs.
• Provide training to CRAs and collaborate with Project Management to optimize recruitment and data quality.

Skills

Excellent planning and organizational

English communication

Lead remotely

Education

Four-year college degree in biological/physical/health studies

Two-year college degree (nursing or life science) with experience

Tools

Microsoft Office

eCRF

IVRS

IxRS/CTMS/EDC

Job description

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate to lead site management activities across a geographic region, ensuring protocol compliance and timely delivery of study milestones.

You will supervise site qualification, initiation, monitoring and close-out, provide training to CRAs, and collaborate with project management to optimize recruitment and data quality. Travel required; a four-year degree and CRA experience are expected.