Not specified; annual incentive plan bonus availab...
Fully remote
Ich-gcp guidelines compliance
Risk based monitoring approach
Site process specialist duties
The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines
Job Summary
The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines.
Employees will conduct remote or on-site visits to assess protocol adherence, manage documentation, and ensure audit readiness across global locations.
Thermo Fisher Scientific offers comprehensive health benefits, flexible work arrangements, and generous leave policies including paid birthday and parental leave.
Matching Summary
The role involves performing and coordinating clinical monitoring and site management processes to ensure trial compliance with ICH-GCP guidelines.
Salary
Not specified; Annual incentive plan bonus available; Competitive remuneration offered
Skills & Requirements
Must-have
ICH-GCP guidelines compliance
Risk Based Monitoring approach
Site process specialist duties
Protocol adherence verification
Data accuracy through SDV/SDR
Nice-to-have
Root cause analysis skills
Collaborative relationship building
Critical thinking and problem solving
Flexible and adaptable mindset
Strong presentation skills
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
1 year experience as a clinical research monitor or PPD Drug Development Fellowship
Valid driver's license where applicable
Australian citizenship or permanent residency required
Work Rights
Australian citizenship or permanent residency required