Senior Clinical Research Associate — Hybrid/Remote Trials

7Learnings

Brisbane

Hybrid

AUD 90,000 - 150,000

Full time

47 hours ago
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Benefits offered by this job

Annual leave
Health insurance
Retirement plan
Global EAP LifeWorks

Job summary

ICON Plc in Australia is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities in a sponsor-dedicated model. The role requires monitoring sites, ensuring protocol and GCP compliance, and collaborating with cross-functional teams to ensure data integrity and timely reporting.

The Senior CRA will travel approximately 60% to sites, work in a hybrid environment, and contribute to continuous improvement initiatives while supporting trial execution across

Qualifications

  • Bachelor's degree in a relevant scientific field.
  • Extensive experience as a Clinical Research Associate with regulatory knowledge.
  • Ability to manage multiple sites and projects concurrently.
  • Experience with monitoring practices and data integrity.

Responsibilities

  • Monitor clinical trial sites to ensure adherence to study protocols and GCP.
  • Conduct site visits to assess performance and resolve issues.
  • Collaborate with cross-functional teams for timely data collection and reporting.
  • Provide training to site staff on trial conduct and compliance.
  • Build and maintain relationships with site personnel and stakeholders.

Skills

Clinical trial monitoring
Regulatory compliance
Data integrity
Stakeholder management

Education

Bachelor's degree in a relevant scientific discipline

Tools

EDC systems
CTMS

Job description

ICON Plc in Australia is seeking a Senior Clinical Research Associate to oversee and manage clinical trial activities in a sponsor-dedicated model. The role requires monitoring sites, ensuring protocol and GCP compliance, and collaborating with cross-functional teams to ensure data integrity and timely reporting.

The Senior CRA will travel approximately 60% to sites, work in a hybrid environment, and contribute to continuous improvement initiatives while supporting trial execution across

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