Senior Clinical Research Associate - Remote

Parexel; Harrisburg (Dauphin County); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites, monitor trial progress, and oversee close-out activities in accordance with GCP and Sponsor standards.

You will be responsible for enrollment support, site execution, and ensuring patient safety across assigned studies. The role requires strong communication with the study team, ability to travel frequently, and collaboration with Site Care Partners to ensure high-quality trial conduct and site

Qualifications

• Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations.
• Monitoring Experience: Minimum 2 years relevant experience in clinical research site monitoring.
• Must be fluent in English and in the native language(s) of the country they will work in.
• Ability to travel 60-80%.
• Valid driver’s license and passport required.

Responsibilities

• Ensure proper conduct of clinical trials in accordance with the SMP, GCP and Sponsor's standards to achieve project goals, timelines and quality.
• Manage operational aspects for site activation through database lock, ensuring timelines and quality deliverables.
• Serve as primary contact for assigned investigator sites and coordinate with the SCP to ensure site delivery quality.
• Interface with study team, vendors, and investigator sites to facilitate information flow.
• Perform investigator site development, coaching and training to ensure protocol compliance and patient safety.

Skills

Clinical trial methodologies

ICH/GCP

FDA regulations

English fluency

Travel readiness

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites, monitor trial progress, and oversee close-out activities in accordance with GCP and Sponsor standards.

You will be responsible for enrollment support, site execution, and ensuring patient safety across assigned studies. The role requires strong communication with the study team, ability to travel frequently, and collaboration with Site Care Partners to ensure high-quality trial conduct and site