Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary with a focus on rewarding high performance
- Generous annual leave entitlements to support work-life balance
- Comprehensive health insurance options tailored to you and your family’s needs
- Flexible benefits including childcare vouchers and discounted gym memberships
- Opportunity for career advancement within a diverse and inclusive culture
- Access to a Global Employee Assistance Programme for well-being support

What to Expect (Job Responsibilities):
- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process
- Collaborate with investigators and site staff to facilitate smooth study conduct
- Perform data review and resolution of queries to maintain high-quality clinical data
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports

What is Required (Qualifications):
- Bachelor's degree in a scientific or healthcare-related field highly preferred
- Minimum of 2 years of experience as a Clinical Research Associate, with on-site monitoring experience required
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills, with attention to detail
- Ability to work independently and collaboratively in a fast-paced environment

How to Stand Out (Preferred Qualifications):
- Experience in conducting clinical trials across various therapeutic areas
- Familiarity with electronic data capture systems and clinical trial management software
- Ability to mentor or train junior staff members
- Strong problem-solving skills and adaptability in changing environments

#ClinicalResearch #CareerOpportunity #HealthInsurance #DiversityAndInclusion #WorkLifeBalance

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