Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate to join our passionate team in St Albans. This role involves monitoring clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to enhance research initiatives.

Responsibilities

• Conduct training sessions for site staff on study protocols.
• Ensure compliance with ethical guidelines and regulatory standards.
• Collaborate with cross-functional teams to support research initiatives.
• Prepare site visit reports and follow up on action items.
• Assist in resolving issues related to data discrepancies or protocol deviations.
• Promote patient safety and ethical conduct throughout the trial process.
• Manage trial supplies and ensure appropriate storage conditions.

Requirements

Education

• Bachelor's degree in Nursing or Clinical Research
• Master's degree in relevant discipline is preferred

Experience

• 3+ years of clinical research experience is preferred

Technical Skills

• Data Analysis
• Study Design

Soft Skills

• Problem-solving
• Teamwork

Certifications

• Certified Clinical Research Associate (CCRA)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Previous experience in oncology clinical trials: Experience working specifically in oncology will be an advantage.
• Knowledge of biostatistics: Understanding of biostatistical methods would be beneficial.

Benefits

• Comprehensive healthcare plan
• 401(k) retirement plan
• Annual salary review
• Company-sponsored training and conferences

Company Culture

• Continuous Learning: Our team is committed to continuous learning and development in the field of clinical research.
• Diversity and Inclusion: We celebrate diversity and work to create an inclusive environment for all employees.
• Employee Wellbeing: We prioritize the wellbeing of our employees through various support programs.