Clinical Research Associate, I

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

📋 Description

• Conduct and document various types of onsite monitoring visits.

• Engage in study initiation processes, when relevant.

• Execute CRF assessment, verify source documents, and resolve queries.

• Oversee communication with clinical sites.

• Act as a liaison for in-house support services and vendors.

• Update internal project teams about the progress of the study.

• Take part in feasibility assessments.

• Assist the regulatory team in preparing submission documents for studies.

• Establish and nurture relationships with clinical sites and investigators.

• Prioritize the rights, safety, and welfare of subjects, ensuring compliance with data quality standards.

• Guarantee adherence to timelines, objectives, and standards of clinical research projects.

⛳️ Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training, and experience.

• Experience in Clinical Research or a Medical environment.

• Independent onsite monitoring experience within the UK.

• Proficient PC skills, particularly in MS Word, Excel, and PowerPoint.

• Capability to plan, manage multiple tasks, and work effectively in a dynamic team setting.

• Strong communication, collaboration, and problem-solving abilities.

• Willingness to travel.

• Valid driver's license.

🏝️ Benefits

• Full-time employment.

• Option for remote work.

• Support from an experienced and professional team.

• Opportunities to develop a diverse range of skills.

• Potential for career advancement within the company.

• Involvement in comprehensive and challenging projects.