We are looking for a Clinical Research Associate in Southampton to join our innovative team. The successful candidate will be involved in planning, conducting, and monitoring clinical trials while ensuring compliance with regulatory standards.
Responsibilities
Work closely with clinical research coordinators and investigators to ensure smooth operation of trials.
Document and track all site correspondence and communications.
Conduct regular audits of sites to ensure compliance with clinical trial standards.
Facilitate effective communication between team members and external stakeholders.
Conduct training sessions for new staff on clinical trial protocols and compliance regulations.
Requirements
Education
Master's degree in Clinical Research or related field
PhD level education is a plus
Experience
3+ years of experience in a clinical research role
Technical Skills
Clinical Trial Regulations
Regulatory Submissions
Soft Skills
Leadership
Adaptability
Certifications
Clinical Research Coordinator Certification
ISO 14155 Certification
Languages
English: Fluent
Advantageous
Experience in oncology clinical trials: Specific experience in conducting and monitoring oncology-related studies.
Familiarity with patient recruitment strategies: Knowledge of effective patient recruitment methods for clinical trials.
Benefits
Salary package above industry standards
Comprehensive healthcare coverage
Employee wellness programmes and mental health support
Opportunities for career progression within the organisation
Company Culture
Employee Empowerment: We empower our employees to take initiative and make decisions that drive our success.
Supportive Team Dynamics: Our team dynamics are supportive, ensuring all voices are heard and valued.
Focus on Wellness: We prioritise the well-being of our team members and provide resources to support mental health.