Clinical Research Associate 1

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Execute clinical trial monitoring tasks with exceptional quality.

• Ensure that studies are performed in accordance with study protocols, operational procedures, and good clinical practices.

• Verify product performance assertions.

• Provide data necessary for important regulatory submissions.

• Establish the functional and clinical usefulness of investigational products.

• Comprehend and apply federal regulations effectively.

• Assist in implementing standard operating procedures to guarantee compliance with FDA regulations, GCP, IVD directives, and client policies.

• Collaborate closely with the team and stakeholders.

• Lead the design, planning, coordination, and execution of activities related to initiating, monitoring, and completing clinical research studies for in vitro diagnostics.

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field.

• Relevant experience in in vitro diagnostics, preferably with a laboratory background.

• Practical understanding of in vitro diagnostics and clinical trial methodologies.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills for effectively addressing inquiries in a timely manner.

• Willingness to travel as needed, primarily from a UK base, and occasionally internationally.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs that include medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career progression.

• Flexible remote/home-based work arrangements.