Senior CRA: Remote Site Monitoring & Trial Delivery

Parexel; Cheyenne (WY); On-site; USD 90,000 - 130,000; Full time

Job summary

Parexel FSP is seeking a Senior Clinical Research Associate (Sr. CRA) to join our US team. The Sr. CRA will oversee site management, monitoring, and close-out of trials to ensure patient safety and quality in line with GCP and client standards.

The role requires strong knowledge of clinical trial processes, 3+ years monitoring experience, and willingness to travel 60-80% within the area. Fluency in English is essential.

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Monitoring experience: minimum 3 years in clinical research site monitoring (preferably 2 years in Oncology).
• Therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases is preferred.

Responsibilities

• Oversee site monitoring and conduct in accordance with SMP and SOPs.
• Act as primary point of contact for investigator sites and coordinate with the Site Care Partner.
• Perform onsite and remote monitoring, ensure data quality and patient safety; manage site issues and CAPAs.

Skills

Clinical monitoring

GCP knowledge

English proficiency

Education

Bachelor’s degree in life sciences

Job description

Parexel FSP is seeking a Senior Clinical Research Associate (Sr. CRA) to join our US team. The Sr. CRA will oversee site management, monitoring, and close-out of trials to ensure patient safety and quality in line with GCP and client standards.

The role requires strong knowledge of clinical trial processes, 3+ years monitoring experience, and willingness to travel 60-80% within the area. Fluency in English is essential.