The CRA anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends and communicates corrective action as indicated. The CRA should use functional expertise and exercise good judgment in seeking appropriate guidance and ensures that follow-up to all corrective action is taken at the clinical site and is properly documented.

Must Haves:

• High School Diploma and at least 5 years of CRA experience
• Clinical research monitoring experience
• Decentralized/hybrid clinical trials experience- multiple locations
• In-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials
• Knowledge of regulations governing clinical research, ICH/GCP Guidelines, US CFR, HIPAA and other applicable regulations
• Experience in on-site/remote monitoring of investigational drug or device trials in accordance with company Standard Operating Procedures and FDA regulations is required
• Experience overseeing multiple clinical trials concurrently, while maintaining attention to detail
• Experience with the review of CRFs (paper or electronic) and subject source documentation is a must

Job Type: Contract

Pay: $45.00 - $58.00 per hour

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Vision insurance

Experience level:

• 3 years

Schedule:

• Monday to Friday

Education:

• High school or equivalent (Required)

Experience:

• Clinical research: 3 years (Required)
• Clinical trials: 3 years (Required)

Ability to Commute:

• Atlantic City, NJ 08401 (Required)

Ability to Relocate:

• Atlantic City, NJ 08401: Relocate before starting work (Required)

Work Location: In person