Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate to oversee clinical trials and ensure compliance with regulatory standards. The ideal candidate will be passionate about medical research and demonstrate excellent analytical and problem-solving skills.

Responsibilities

• Help develop and implement study protocols and informed consent documents.
• Collaborate with data management teams to ensure data quality.
• Prepare periodic progress reports for study stakeholders.
• Identify and mitigate risks associated with clinical trials.
• Stay informed of industry trends and regulatory changes.
• Contribute to post-study evaluations and reporting.

Requirements

Education

• Bachelor's degree in Biomedical Science or related field
• PhD is an asset

Experience

• 3+ years of experience in clinical trials or research

Technical Skills

• Regulatory submissions
• Research methodology

Soft Skills

• Problem-solving
• Teamwork

Certifications

• Certified Clinical Research Coordinator (CCRC)

Languages

• English: Fluent

Advantageous

• Experience in pharmacovigilance: Familiarity with drug safety and reporting requirements.
• Knowledge of therapeutic areas: Understanding of various therapeutic areas like oncology or cardiology.

Benefits

• Comprehensive health benefits
• Pension scheme with employer contribution
• Opportunity for remote work up to two days a week
• Access to wellness programs

Company Culture

• Innovation: Our culture encourages innovative thinking and creativity to drive impactful research.
• Diversity and Inclusion: We strive for a diverse workforce and inclusive atmosphere where everyone can thrive.
• Work-Life Balance: Promoting a healthy work-life balance is a priority, ensuring employee well-being.