Clinical Research Associate

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

📋 Description

• Oversee clinical trial locations to guarantee adherence to study protocols, ICH-GCP guidelines, and regulatory standards.

• Perform on-site visits throughout the South West UK area, assisting study sites and resolving operational challenges.

• Collaborate with cross-functional teams to ensure the precise and timely collection and reporting of study data.

• Establish and nurture strong working relationships with investigators, site personnel, and other essential stakeholders.

• Offer guidance and support to site staff, aiding in the successful execution of clinical trials.

⛳️ Requirements

• A degree in Life Sciences, Nursing, Medicine, or a related field.

• Prior experience as a Clinical Research Associate in oncology studies within the UK.

• Comprehensive understanding of clinical trial processes, regulatory obligations, and Good Clinical Practice (GCP).

• Exceptional organizational abilities, with a knack for managing multiple sites and priorities efficiently.

• Demonstrated experience in site management and monitoring activities, ensuring the delivery of high-quality studies.

• Strong communication skills and the ability to build effective relationships.

• Willingness and capability to travel to sites throughout the UK, possessing a valid driving licence.

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellbeing initiatives, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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