Clinical Research Coordinator

Job Description

We are seeking a Clinical Research Coordinator to play a pivotal role in managing clinical trials and research projects. The successful candidate will oversee study protocols, ensure compliance with regulatory requirements, and facilitate communication between stakeholders, contributing significantly to the advancement of medical knowledge.

Responsibilities

• Lead the planning and execution of clinical trials, ensuring effective participant recruitment.
• Maintain regulatory compliance through effective monitoring and reporting.
• Develop and manage timelines for project deliverables.
• Coordinate with external vendors and partners involved in research projects.
• Analyze and interpret data, preparing findings for publication and presentation.

Requirements

Education

• Bachelor's degree in Medicine or Nursing
• Advanced degree is a plus

Experience

• 5+ years experience in clinical research and project management

Technical Skills

• Regulatory Compliance
• Project Management

Soft Skills

• Analytical Skills
• Leadership

Certifications

• Clinical Research Associate (CRA) Certification
• Project Management Professional (PMP) Certification

Languages

• English: Fluent

Advantageous

• Familiarity with project management tools: Experience in using tools like Trello, Asana, or similar for tracking project progress.
• Previous experience in a healthcare setting: Experience working within hospitals or medical centres is advantageous.

Benefits

• Health, dental, and vision coverage
• Generous superannuation contributions
• Employee wellness programs and support
• Opportunities for career advancement

Company Culture

• Continuous Improvement: We strive for excellence through continuous improvement in our processes and practices.
• Inclusiveness: Diversity and inclusivity are central to our work environment, where every voice is important.
• Supportive Environment: We provide a supportive environment where professional growth and well-being are prioritized.