Responsibilities: of the Clinical Research Associate II: Oversee the development and execution of clinical trial plans and protocols for Phase I-IV studies Maintain documentation and data evaluations Work collaboratively with the team to ensure monitoring activities meet study requirements Conduct on-site monitoring visits and field evaluations Qualifications: of the Clinical Research Associate II: 3+ years of on-site clinical monitoring experience within General Medicine or related therapeutic areas Experience with the FDA or similar regulatory and accrediting agencies Bachelor's degree in Life Sciences or a related field Prior experience at a larger CRO preferred Compensation: for the Clinical Research Associate II: Salary Range: $120,000-$145,000 Comprehensive Benefits: Medical, Dental, Vision, 401(k), PTO, bonuses, and sick leave if required by law This job opens for applications on 10/16. Applications for this job will be accepted for at least 30 days from the posting date.
| Location | Raleigh, NC |
| Salary | $120,000–$145,000 Per Year |
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