Senior Clinical Trials Site Lead

Parexel; Topeka (KS); On-site; USD 90,000 - 120,000; Full time

Job summary

Parexel seeks a Senior Clinical Research Associate to lead site management and monitoring for oncology trials. The role ensures patient safety, data integrity, and regulatory compliance across sites, with close collaboration to the SCP and study team.

Ideal candidates have 3+ years in site monitoring, deep ICH/GCP knowledge, and the ability to travel extensively within the region. English fluency is required, with local language proficiency advantageous.

Qualifications

• 3+ years of clinical research site monitoring experience (oncology preferred)
• Strong knowledge of ICH/GCP and regulatory requirements
• Fluent in English and the local language where assigned to work
• Willingness to travel 60–80% within area

Responsibilities

• Manage investigator site monitoring from activation to database lock
• Ensure patient safety and data quality per SMP and SOPs
• Provide site coaching, training, and issue resolution with SCP and study team
• Maintain TMF and site documentation within required timelines
• Support site close-out activities and site performance improvements
• Collaborate with Drug Safety and other functional areas as needed

Skills

Monitoring experience

GCP/ICH knowledge

Oncology experience

Global trial experience

English fluency

Travel readiness

Education

Bachelor’s degree in life sciences

Job description

Parexel seeks a Senior Clinical Research Associate to lead site management and monitoring for oncology trials. The role ensures patient safety, data integrity, and regulatory compliance across sites, with close collaboration to the SCP and study team.

Ideal candidates have 3+ years in site monitoring, deep ICH/GCP knowledge, and the ability to travel extensively within the region. English fluency is required, with local language proficiency advantageous.