Travel-Ready Clinical Research Associate II

Parexel; Atlanta (GA); On-site; USD 75,000 - 120,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate (CRA) to monitor investigator sites and manage study quality in line with GCP and sponsor standards. The CRA will conduct site initiation, ongoing monitoring, and close-out activities, ensuring patient safety and data integrity across trials.

The role requires 2+ years of monitoring experience, strong knowledge of ICH/GCP and FDA regulations, and the ability to travel 60–80% with a valid driver's license.

Qualifications

• Extensive knowledge of clinical trial methodologies and ICH/GCP.
• Understanding of FDA regulations and local country requirements.
• Minimum 2 years' monitoring experience in clinical research.
• Must be fluent in English and local language(s).
• Ability to travel 60–80%.

Responsibilities

• Ensure proper conduct of clinical trials in accordance with SMP, laws, GCP, and sponsor standards to achieve goals.
• Manage operational aspects for site activities from activation to database lock with timelines and quality.
• Serve as the primary contact for assigned investigator sites; coordinate with SCP to ensure quality of site delivery.
• Interface with study team to facilitate information flow between vendors and investigator sites.
• Provide investigator site development and training to ensure protocol compliance and patient safety.
• Attend investigator meetings; support enrollment and recruitment initiatives at site level.

Skills

Clinical trial knowledge

ICH/GCP

FDA regulations

Site monitoring

Travel 60-80%

English fluency

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Clinical Research Associate (CRA) to monitor investigator sites and manage study quality in line with GCP and sponsor standards. The CRA will conduct site initiation, ongoing monitoring, and close-out activities, ensuring patient safety and data integrity across trials.

The role requires 2+ years of monitoring experience, strong knowledge of ICH/GCP and FDA regulations, and the ability to travel 60–80% with a valid driver's license.