CRA II: Remote & Onsite Monitoring for Breakthrough Trials

11 Premier Research International LLC; Pennsylvania; On-site; USD 72,000 - 88,000; Full time

Benefits offered by this job

Health insurance

Retirement plans

Paid time off

Job summary

Premier Research is seeking a Clinical Research Associate II to join our Northeast US team. The CRA II will monitor Phase I–IV trials and device studies, both on-site and remotely, ensuring data integrity and patient safety in compliance with ICH-GCP/ISO requirements.

You will interact with investigative sites, vendors, and clients while managing study timelines and budgets. Password-protected details include travel of 70-85% and a base pay around market standards.

Qualifications

• Undergraduate degree required or international equivalent.
• Minimum of 18+ months on-site clinical research monitoring experience.

Responsibilities

• Perform monitoring activities (on-site and remote) for Phase I–IV trials and device studies.
• Serve as primary contact for investigative sites and manage query resolution.
• Ensure data validity, accuracy, and timeliness in line with trial protocol and GCP/ISO requirements.
• Identify risks and provide retraining opportunities for sites.
• Plan and schedule day-to-day monitoring visits and complete high-quality trip reports.

Skills

On-site monitoring

Customer focus

Communication skills

Education

Undergraduate degree

Job description

Premier Research is seeking a Clinical Research Associate II to join our Northeast US team. The CRA II will monitor Phase I–IV trials and device studies, both on-site and remotely, ensuring data integrity and patient safety in compliance with ICH-GCP/ISO requirements.

You will interact with investigative sites, vendors, and clients while managing study timelines and budgets. Password-protected details include travel of 70-85% and a base pay around market standards.