Lead Clinical Research Associate – Global Trials Oversight

Worldwide Clinical Trials; United States; Remote; USD 90,000 - 150,000; Full time

Job summary

Worldwide Clinical Trials is a global midsize CRO with 3,500+ experts committed to improving lives through high-quality clinical research. We seek a Lead Clinical Research Associate to manage site qualification, initiation, monitoring, and close-out visits across global studies, ensuring data integrity and patient safety.

You will mentor CRAs, collaborate with project teams, and contribute to protocol and CRF design while upholding regulatory standards and site training.

Qualifications

• MD/PharmD or equivalent with 3+ years as a CRA
• Active monitoring and site management experience
• Fluent in local languages and English

Responsibilities

• Perform site qualification, initiation, interim monitoring, management and close-out visits
• Develop Monitoring Plan and review site visit reports
• Mentor junior CRAs and site staff
• Coordinate with Project Management on milestones
• Maintain regulatory documents and TMF filings
• Ensure data quality and safety reporting according to GCP

Skills

Communication

Planning & organization

Interpersonal skills

Problem solving

Leadership

Process improvement

Clinical research principles

FDA/EU regulations

Team coordination

Education

MD or PharmD or equivalent

Lifesciences bachelor degree or higher

Nursing degree or related life science degree

Tools

IxRS

EDC systems

Microsoft Office

Job description

Worldwide Clinical Trials is a global midsize CRO with 3,500+ experts committed to improving lives through high-quality clinical research. We seek a Lead Clinical Research Associate to manage site qualification, initiation, monitoring, and close-out visits across global studies, ensuring data integrity and patient safety.

You will mentor CRAs, collaborate with project teams, and contribute to protocol and CRF design while upholding regulatory standards and site training.