Clinical Research Coordinator

Job Description

We are seeking a detail-oriented Clinical Research Coordinator to oversee and manage clinical trials in Bunbury. The ideal candidate will possess a strong understanding of clinical protocols and an aptitude for data management and patient interaction. Your role will be pivotal in ensuring trials are conducted efficiently and ethically.

Responsibilities

• Manage budget and resources for clinical trials.
• Liaise with sponsors and stakeholders throughout the study lifecycle.
• Implement corrective actions to resolve compliance issues.
• Prepare regulatory submissions and maintain trial master files.
• Ensure participant safety and project timelines are met.
• Create and disseminate trial materials and questionnaires.
• Report trial results to key stakeholders.
• Facilitate communication between site staff and study sponsors.
• Prepare and deliver presentations on trial outcomes.
• Conduct analysis to evaluate trial effectiveness.

Requirements

Education

• Bachelor's degree in Life Sciences, Nursing, or related field
• Master's degree in Public Health or Clinical Research is preferred

Experience

• 3-5 years of experience in clinical or medical research

Technical Skills

• Statistical Analysis
• Project Management

Soft Skills

• Organisational Skills
• Interpersonal Skills

Certifications

• Clinical Research Associate (CRA) Certification
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with statistical software (e.g., SPSS or SAS): Ability to perform complex data analyses and reporting.
• Knowledge of medical terminology and clinical research protocols: Strong foundation in medical language and research methodologies.

Benefits

• Comprehensive health and wellness benefits
• 401(k) retirement plan with employer match
• Flexible work hours with a focus on work-life balance
• Ongoing training and professional development opportunities

Company Culture

• Respect for Diversity: We value diversity in our team and strive for inclusivity in all aspects.
• Continuous Learning: Our staff engages in continuous learning opportunities to advance their skills.
• Patient-Centric Approach: We always keep the patient at the forefront of our research activities.