Clinical Research Associate will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to succesffuly create lifesaving drugs and treatments
Responsibilities of the Clinical Research Associate:- Oversee the development and execution of the clinical trial plans and protocols for Phase I-IV
- Maintain documentation and data evaluations
- Work collaboratively with the team to ensure monitoring activities meet study requirements
- Conduct on site field evaluations
Qualifications of the Clinical Research Associate:- 3+ years of on-site clinical monitoring experience, specifically within Oncology
- Experience with the FDA or similar Regulatory and Accrediting administrations
- Bachelor's degree in one of the life sciences or related background
- Prior experinece at a larger CRO preferred
Compensation for the Clinical Research Associate:- Salary Range: $120,000-$145,000
- Comprehensive Benefits: Medical, Dental, Vision, 401k, PTO, bonuses, and sick leave if required by law
This job opens for applications on 8/21. Applications for this job will be accepted for at least 30 days from the posting date.Keywords: Clinical Research Associate, CRA, BA, life sciences, clinical trials, phases, documentation, data, monitor, study, onsite, FDA, drugs, treatments, medical, dental, vision, oncology, tumor, cancer, 401k, PTO, Holiday,
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