Senior Clinical Research Associate – Remote

Parexel; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Parexel FSP is seeking a Senior Clinical Research Associate to join our US team. The Sr. CRA will oversee site monitoring and closure of trials, ensuring patient safety and data quality in line with GCP and client standards.

The role requires strong monitoring experience, oncology exposure preferred, and frequent travel (60–80%). You will collaborate with the SCP and broader study team to drive site performance and regulatory compliance.

Qualifications

• Minimum 3 years of clinical research site monitoring experience.
• Oncology experience preferred.

Responsibilities

• Ensure proper conduct of clinical trials per SMP, laws, GCP and client standards.
• Manage site activation through database lock with timelines and quality deliverables.
• Serve as primary contact for investigator sites, coordinating with SCP and study team.
• Facilitate information flow between study team, vendors and sites.
• Provide investigator site development and protocol training to site staff.
• Attend investigator meetings and support enrollment initiatives at site level.
• Conduct onsite and remote monitoring in line with SMP and SOPs.
• Monitor and address SAEs/AE reporting and required documentation.
• Prepare and submit TMF, site reports, deviations and recruitment metrics within deadlines.
• Identify and resolve site issues with CAPA and corrective actions.
• Oversee investigational product handling at sites and support database release.

Skills

Clinical monitoring

GCP knowledge

FDA/regulatory knowledge

Oncology experience

Global trials

Education

Bachelor's degree in life sciences

Job description

Parexel FSP is seeking a Senior Clinical Research Associate to join our US team. The Sr. CRA will oversee site monitoring and closure of trials, ensuring patient safety and data quality in line with GCP and client standards.

The role requires strong monitoring experience, oncology exposure preferred, and frequent travel (60–80%). You will collaborate with the SCP and broader study team to drive site performance and regulatory compliance.