Clinical Research Associate: Site Monitoring & Coordination

PSG Global Solutions; Tucson (AZ); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading healthcare consulting firm in the United States is seeking a Clinical Research Associate to conduct vital clinical study activities. You will collaborate closely with project teams, ensuring compliance with Good Clinical Practices while monitoring study execution. Candidates should have a Bachelor of Science and at least 2 years of coordination experience in the pharmaceutical or medical device sectors. This role offers a dynamic environment with potential travel up to 30%.

Qualifications

• 2+ years of clinical study coordination or monitoring experience required.
• Knowledge of cGCP and CFR preferred.
• Background in biomedical or healthcare services with lab experience is advantageous.

Responsibilities

• Conducts clinical study monitoring and reporting.
• Assists in study preparation and execution.
• Participates in team activities and meetings.

Skills

Clinical study coordination

GCP adherence

Communication skills

Organization

Detail orientation

Education

Bachelor of Science, RN, or BSN

Tools

Microsoft Word

Microsoft Excel

Access

PowerPoint

Job description

A leading healthcare consulting firm in the United States is seeking a Clinical Research Associate to conduct vital clinical study activities. You will collaborate closely with project teams, ensuring compliance with Good Clinical Practices while monitoring study execution. Candidates should have a Bachelor of Science and at least 2 years of coordination experience in the pharmaceutical or medical device sectors. This role offers a dynamic environment with potential travel up to 30%.