Base: not specified; bonus/equity: annual incentiv...
Fully remote
Risk-based monitoring approach
Protocol and regulatory compliance
Clinical trial site initiation
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale
Job Summary
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale.
The role involves performing and coordinating clinical monitoring and site management processes to ensure trials are conducted according to protocol and regulatory standards.
Thermo Fisher Scientific offers competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits within an innovative and forward-thinking organization.
Matching Summary
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale.
Salary
Base: Not specified; Bonus/Equity: Annual incentive plan bonus; Benefits: Healthcare and employee benefits
Skills & Requirements
Must-have
Risk-based monitoring approach
Protocol and regulatory compliance
Clinical trial site initiation
Data accuracy through SDR and SDV
Audit readiness and documentation
Investigator site collaboration
Nice-to-have
Critical thinking and root cause analysis
Good digital literacy and Microsoft Office skills
Effective interpersonal and communication skills
Ability to work independently or in a team
Attention to detail and organizational skills
Presentation skills
Key Requirements
Bachelor's degree in life sciences or equivalent
Registered Nursing certification or equivalent
Minimum 1 year clinical research monitoring experience
Valid driver's license
Knowledge of ICH-GCP guidelines and applicable regulations