Clinical Research Associate II will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to successfully create lifesaving drugs and treatments.
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.
Keywords: Clinical Research Associate, CRA II, CRA, Clinical Monitoring, General Medicine, Clinical Trials, Phase I, Phase II, Phase III, Phase IV, Site Monitoring, FDA, CRO, Drug Development, Regulatory Compliance, Life Sciences, Pharmaceuticals, Biotechnology, Medical, Dental, Vision, 401(k), PTO, Holidays
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