
Senior Clinical Research Coordinator
2 weeks ago
Key Role in Clinical Research: We are seeking an experienced Senior Clinical Research Associate to join our team.
Job Description:
- Conduct on-site visits, monitor study progress, and ensure compliance with GCP/ICH standards.
- Develop and implement subject recruitment strategies to meet project goals.
- Collaborate with site teams to deliver protocol training and build strong relationships.
- Track study documentation, maintain Trial Master Files, and ensure audit-readiness.
- Mentor junior clinical staff and contribute to a culture of excellence and learning.
Qualifications:
- Minimum 5 years of independent on-site monitoring experience with at least 3 years in oncology.
- Deep knowledge of GCP, ICH, and clinical trial regulations.
- Strong therapeutic area expertise and protocol understanding.
- Excellent communication, organization, and problem-solving skills.
Benefits:
- Gain direct experience working with a leading global contract research organization.
- Access world-class training and mentoring opportunities.
- Work in a dynamic role that drives innovation and excellence in clinical research.
Other Opportunities:
- Enjoy the stability and resources of a leading global company.
- Develop your career in a wide variety of therapeutic areas.
- Be part of a collaborative cross-functional team.
Requirements:
- Minimum 5+ years of experience in clinical research.
- Ability to work independently and collaboratively as part of a team.
- Proactive mindset and ability to build strong relationships with stakeholders.
Location: Melbourne is the preferred location, but Sydney can be considered. Remote work options may be available for experienced candidates.
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