Senior Clinical Research Associate

About this role

📋 Description Ensure successful protocol level execution of SMM deliverables involving start-up, execution, and Ensure site related study execution including monitoring visits, site evaluations, site selection Anticipate and identify site issues that could affect timelines and develop alternative solutions. Maintain and keep current clinical trial management systems with site-specific information. Provide local regulatory and legal requirement expertise.

Ensure timely payment execution for assigned sites/studies according to clinical study agreements 🎯 Requirements Bachelors or equivalent degree, health related (e.g., Medical, Scientific, Nursing, Pharmacy) Site Monitoring Experience: Minimum 3 years. Strong analytical and critical thinking skills to evaluate complex issues from multiple Excellent interpersonal skills with the ability to communicate persuasively and with clarity.

Flexibility and adaptability to changing requirements, resourcefulness, and creativity. Demonstrated proactive and positive team player. 🎁 Benefits Equal Opportunity Employer Commitment to operating with integrity, driving innovation, transforming lives, and serving

Source listing: empllo_remote