Remote CRA II: Site Monitoring & Study Mgmt

Parexel; Cheyenne (WY); Remote; USD 70,000 - 95,000; Full time

Job summary

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all trial phases. You will ensure data integrity, subject safety, and regulatory compliance while coordinating with sponsor teams.

You will conduct remote and on-site monitoring, train site staff, and manage regulatory documentation. Strong communication, attention to detail, and independence are essential for success.

Qualifications

• Minimum 2 years of direct site monitoring experience in bio/pharma/CRO.
• Experience with site start-up, maintenance and close-out processes.
• Strong understanding of ICH-GCP and regulatory requirements.

Responsibilities

• Acts as primary site contact and site manager across study phases.
• Performs remote and on-site monitoring to ensure data integrity and subject safety.
• Collects regulatory documentation and maintains trial master file.
• Communicates with investigators and site staff on protocol and regulatory issues.
• Identifies and resolves site performance or compliance problems.
• Maintains documentation in CTMS and other systems per timelines.

Skills

Site management

GCP/ICH compliance

Clinical monitoring

Regulatory documentation

Data review

Stakeholder communication

Issue resolution

Independent judgement

Education

Bachelor’s degree in science or biology

Job description

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager across all trial phases. You will ensure data integrity, subject safety, and regulatory compliance while coordinating with sponsor teams.

You will conduct remote and on-site monitoring, train site staff, and manage regulatory documentation. Strong communication, attention to detail, and independence are essential for success.