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Job Description
- Req#: JR138440
Employer Industry: Clinical Research and Healthcare Intelligence
Why consider this job opportunity:
- Competitive salary with additional benefits focused on well-being and work-life balance
- Opportunity for career advancement and growth within a reputable organization
- Flexible working environment with various annual leave entitlements
- Comprehensive health insurance offerings to suit personal and family needs
- Access to a Global Employee Assistance Programme for support and well-being
- Inclusive and diverse workplace culture that values high performance and nurtures talent
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 resolve 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
- Minimum of 12 months onsite monitoring experience as a Clinical Research Associate (CRA I, CRA II, or Senior CRA)
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
- Strong organizational and communication skills with attention to detail
- Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license
How to Stand Out (Preferred Qualifications):
- Experience working in a fast-paced environment
- Proficiency in clinical trial management systems and electronic data capture
- Familiarity with regulatory submission processes
- Additional certifications related to clinical research
#ClinicalResearch #HealthcareJobs #CareerGrowth #DiversityAndInclusion #ClinicalTrials
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