Senior CRA – Remote Site Monitoring Lead

Parexel; Jackson (MS); On-site; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites in the US, ensure patient safety, data integrity and quality of study execution.

The role requires extensive monitoring and close collaboration with the Site Care Partner and study team to drive enrollment and site performance. Ideal candidates have 3+ years of site monitoring experience, strong GCP/ICH knowledge, and oncology exposure.

Qualifications

• Bachelor’s degree in life sciences or related field.
• Minimum 3 years clinical monitoring experience.
• Experience in oncology preferred.
• Strong knowledge of GCP/ICH and regulatory requirements.

Responsibilities

• Oversee site monitoring and study conduct to ensure quality and timelines.
• Act as primary contact for investigator sites and coordinate with SCP.
• Ensure TMF and regulatory documentation are completed on time.
• Support site management, patient safety and data integrity across trials.

Skills

GCP/ICH knowledge

FDA regulations

Clinical trials

Oncology experience

Travel readiness

English proficiency

Education

Bachelor’s degree in life sciences or related field

Job description

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites in the US, ensure patient safety, data integrity and quality of study execution.

The role requires extensive monitoring and close collaboration with the Site Care Partner and study team to drive enrollment and site performance. Ideal candidates have 3+ years of site monitoring experience, strong GCP/ICH knowledge, and oncology exposure.