Clinical Research Associate I

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

📋 Description

• Execute and document all forms of onsite monitoring visits

• Participate in study initiation, if applicable

• Conduct CRF assessments, source document verification, and resolve queries

• Manage communication and oversight of site operations

• Act as a liaison for internal support services and vendors

• Update internal project teams on study advancements

• Engage in feasibility studies

• Assist the regulatory team in preparing submissions for studies

• Establish and nurture relationships with clinical sites and investigators

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

⛳️ Requirements

• Bachelor’s degree in Life Sciences or a comparable mix of education, training, and experience

• Experience in Clinical Research or Medical fields

• Independent onsite monitoring experience within the UK

• Proficient PC skills, including MS Word, Excel, and PowerPoint

• Capable of planning, multitasking, and thriving in a fast-paced team environment

• Strong communication, collaboration, and problem-solving abilities

• Willingness to travel

• Possession of a valid driver's license

🏝️ Benefits

• Flexibility to work remotely

• Support from a knowledgeable and professional team

• Opportunity to enhance a variety of skills while advancing within the company

• Involvement in large-scale and challenging projects