Clinical Research Associate
ArteraFull Time
Mid-level (3 to 4 years)
Candidates should possess a BS/BA in a life science or related discipline and have 3 years of experience in the pharmaceutical, biotechnology, or CRO industry, with at least 2 years specifically in clinical monitoring. Experience with ICH GCP guidelines, FDA regulations, and company/sponsor SOPs is essential, along with proficiency in clinical trial management systems.
The Senior Clinical Research Associate will conduct site monitoring responsibilities for clinical trials, providing oversight and guidance to ensure compliance and quality. This includes performing qualification, initiation, interim, and close-out visits, preparing monitoring visit reports, and ensuring data integrity through source document review. The role also involves managing study budgets for stand-alone projects, facilitating ethics document collection and contract negotiation, coordinating with cross-functional departments, and mentoring junior CRAs.
Pharmacy Benefit Management services provider
Abarca Health provides Pharmacy Benefit Management (PBM) services, focusing on flexible and user-friendly solutions for health plans, employers, and government programs like Medicare and Medicaid. Its main product, the Darwin platform, allows clients to quickly implement and modify benefit designs while ensuring compliance with regulations. Abarca Health manages over $5.3 billion in drug spend and processes 100 million prescription claims annually, offering additional services like home delivery for prescriptions. The company's goal is to deliver exceptional service and innovative solutions in the PBM market.