Remote Senior CRA: Site Monitoring & Trial Delivery

Parexel

Dover (DE)

Remote

USD 90,000 - 120,000

Full time

14 days+

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Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to oversee site management, monitoring, and close-out for assigned trials, ensuring patient safety and adherence to GCP and sponsor standards.

The role requires at least 3 years of site monitoring experience (preferably in Oncology), strong knowledge of ICH/GCP and regulatory requirements, and willingness to travel 60–80% across sites. You will collaborate with the SCP and study team, support site development and training, and

Qualifications

Bachelor’s degree in life sciences or related field.
Minimum 3 years clinical site monitoring experience (2+ years in Oncology) in CRO/pharma.
Fluent in English and local language(s) of assignment.
Willingness to travel 60–80%.
Experience with ICH/GCP, FDA regulations and sponsor standards.

Responsibilities

Monitor trial sites from activation through close-out to ensure protocol compliance and data integrity.
Serve as primary contact for investigator sites and coordinate with SCP and study team.
Provide training and development support to site staff and ensure ongoing regulatory compliance.
Prepare and submit site documentation, TMF, and close-out activities.
Address protocol questions and manage site-related risks and issues.