Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary and comprehensive benefits package
- Opportunity for career advancement and growth within the organization
- Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships
- Supportive and diverse workplace culture focused on inclusion and belonging
- 24-hour access to a global network of healthcare professionals through the Global Employee Assistance Programme

What to Expect (Job Responsibilities):
- Monitor clinical research studies involving human subjects from inception to close-out, ensuring adherence to budget and timelines
- Train assigned site staff on study protocols to maintain study and data integrity
- Produce compliance documentation in accordance with regulatory statutes and prepare for potential audits
- Interface with various internal and external stakeholders, including Clinical and Medical Affairs Management
- Create monitoring reports and ensure timely updates in the Clinical Trial Management System (CTMS)

What is Required (Qualifications):
- BS/BA in Scientific or relevant discipline, or 5 years of experience in Clinical Research
- 6-18 months of experience monitoring clinical studies with independent completion of various monitoring activities
- Onsite monitoring experience is mandatory
- Willingness to travel 25% of the time
- Ability to receive guidance and be mentored by senior staff

How to Stand Out (Preferred Qualifications):
- Experience in the Medical Device industry is preferred

#ClinicalResearch #CareerOpportunity #DiversityAndInclusion #HealthcareProfessionals #CompetitiveBenefits

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