Clinical Research Associate

Job Description

Join our vibrant team as a Clinical Research Associate, where you will play an essential role in the entire clinical trial process, including recruitment, data collection, and compliance assurance, thereby contributing to innovative health solutions.

Responsibilities

• Manage clinical trial protocols, procedures, and documentation.
• Coordinate and conduct site monitoring visits.
• Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
• Screen and recruit participants for trials.
• Collect, verify, and report clinical trial data.
• Address and resolve issues at trial sites.
• Collaborate with research teams to ensure smooth operations.
• Train and mentor junior staff and site personnel.
• Prepare reports and presentations for stakeholder meetings.
• Maintain trial supplies and equipment.

Requirements

Education

• Bachelor's degree in Life Sciences or related field
• Relevant qualifications in Clinical Research are an advantage

Experience

• 2+ years of experience in clinical research or related fields

Technical Skills

• Clinical Trial Management
• Data Analysis

Soft Skills

• Detail-oriented
• Communication

Certifications

• Clinical Research Associate Certification (CRA)
• GCP Certification

Languages

• English: Fluent

Advantageous

• Experience with regulatory submissions: Knowledge of regulatory submission processes to health authorities.
• Proficiency in EDC systems: Familiarity with electronic data capture systems.

Benefits

• Competitive salary and performance bonuses
• Health and wellness benefits
• Paid time off and holiday leave
• Opportunities for professional development

Company Culture

• Innovation: We foster a culture of innovation and continuous improvement.
• Collaboration: Our teams work collaboratively to achieve shared goals.
• Integrity: We uphold the highest ethical standards in our research practices.