Employer Industry: Healthcare Intelligence and Clinical Research

Why Consider this Job Opportunity:
- Competitive salary
- Opportunities for career advancement and growth within the organization
- Comprehensive benefits package including health insurance and retirement planning
- Global Employee Assistance Programme for well-being support
- Inclusive and diverse work culture
- Chance to shape the future of clinical development

What to Expect (Job Responsibilities):
- Conduct onsite and remote monitoring activities following ICH-GCP guidelines and applicable regulations
- Verify informed consent procedures and protocol compliance
- Manage investigative site staff to facilitate trial deliverables
- Ensure proper management and accountability of Investigational Product
- Write and submit reports of investigational site findings and update tracking systems

What is Required (Qualifications):
- 2+ years of experience supporting clinical trials with 1+ year of on-site monitoring experience
- In-depth knowledge of drug development process and ICH-GCP
- Strong communication and presentation skills
- Proficiency with Microsoft Office and clinical systems
- Ability to travel extensively

How to Stand Out (Preferred Qualifications):
- Experience as a preceptor, providing training to less experienced clinical team members

#HealthcareIntelligence #ClinicalResearch #CareerDevelopment #CompetitiveSalary #InclusiveWorkCulture

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