Clinical Research Coordinator jobs in Sydney NSW
• The average pay for Clinical Research Coordinator jobs in Sydney NSW is $80K per year.
• Entry-level positions start at $70K per year, while the most experienced workers can earn up to $90K per year.
• Top skills include EXCELLENT COMMUNICATION SKILLS, COMPUTER LITERACY, INTERPERSONAL SKILLS, Clinical trial management and knowledge of GCP.
• Entry-level positions start at $70K per year, while the most experienced workers can earn up to $90K per year.
• Top skills include EXCELLENT COMMUNICATION SKILLS, COMPUTER LITERACY, INTERPERSONAL SKILLS, Clinical trial management and knowledge of GCP.
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+60d ago
Part time
·
Permanent
Similar jobs pay
~$85k - $100k
$85000 - $100000 per annum, Benefits: Competitive salary & benefits
Key points we found
- Join a brand-new clinical research site in Penrith.
- Coordinate clinical trials while ensuring participant care and data quality.
- Flexible work arrangements with opportunities for professional development.
Posted 9d ago
Full time
·
Permanent
Similar jobs pay
~$80k - $100k
Not Applicable
Key points we found
- Coordinate oncology clinical research activities in line with study protocols and regulatory requirements.
- Oversee end-to-end study activities including recruitment, monitoring, and close out.
- Act as a trusted point of contact for patients and stakeholders throughout the clinical trial journey.
Expiring in 3d
Full time
·
Permanent
Similar jobs pay
~$75k - $110k
$75000 - $110000 per annum
Key points we found
- Coordinate participant visits and manage study documentation
- Support protocol implementation and maintain study data accuracy
- Liaise with participants and sponsors to contribute to study delivery
Expiring in 1d
Full time
·
Contract
Similar jobs pay
~$103k - $111k
Pay information not disclosed by advertiser
Key points we found
- Coordinate the day-to-day delivery of clinical trials ensuring compliance with protocols and standards.
- Recruit and support study participants while maintaining a positive experience throughout the trial.
- Manage trial documentation, data collection, and monitor participant safety.