Clinical Research Associate I

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

📋 Description

• Execute and document various types of onsite monitoring visits.

• Engage in study initiation activities, if necessary.

• Conduct CRF assessments, verify source documents, and resolve queries.

• Oversee communication with the study site.

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

• Update internal project teams on study advancements.

• Contribute to feasibility assessments.

• Assist the regulatory team in preparing documents for study submissions.

• Establish and nurture relationships with clinical sites and investigators.

• Prioritize the rights, safety, well-being, and data quality compliance of subjects.

⛳️ Requirements

• Degree in Life Sciences or a comparable combination of education, training, and experience.

• Experience in Clinical Research or Medicine.

• Proven experience in independent onsite monitoring within the UK.

• Proficiency in PC applications, including MS Word, Excel, and PowerPoint.

• Capability to plan, juggle multiple tasks, and collaborate in a dynamic team setting.

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

• Willingness to travel.

• Possession of a valid driver’s license.

🏝️ Benefits

• Option for remote work.

• Full-time employment status.

• Support from a skilled and professional team.

• Opportunities to enhance a diverse range of skills.

• Potential for career advancement within the organization.

• Involvement in large-scale, challenging projects.