Clinical Research Associate

Job Description

We are seeking a Clinical Research Associate to join our dynamic team in Mount Gambier. The successful candidate will be responsible for overseeing clinical trials, ensuring compliance with regulatory requirements, and coordinating with various stakeholders to facilitate research activities.

Responsibilities

• Ensure timely submission of regulatory documents for clinical trials.
• Track trial milestones and timelines, reporting updates to the Research Manager.
• Facilitate communication between study staff and sponsors.
• Implement corrective actions for any protocol deviations identified during audits.

Requirements

Education

• Master's degree in Clinical Research or related field

Experience

• 3+ years of experience in managing clinical trials

Technical Skills

• Data Analysis
• Project Management

Soft Skills

• Critical Thinking
• Interpersonal Skills

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Proficiency in medical writing: Ability to compose clinical study reports and regulatory documents.
• Certification in Good Clinical Practice (GCP): Certification demonstrating knowledge of GCP regulations and guidelines.

Benefits

• Comprehensive health insurance coverage
• Retirement savings plan with employer match
• Work-life balance initiatives
• Continuous education reimbursement

Company Culture

• Ethical Standards: We operate with high ethical standards, ensuring transparency and integrity in all our research.
• Continuous Improvement: We believe in constant learning and improvement, striving for excellence in our research outcomes.
• Inclusivity: Our workplace is inclusive, welcoming diverse perspectives to enhance our research efforts.