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Clinical Research Associate
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Job Description
- Req#: JR143970
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Competitive salary with various annual leave entitlements
- Comprehensive health insurance offerings tailored to you and your family's needs
- Opportunity for career advancement and growth within a global organization
- Flexible country-specific optional benefits, including childcare vouchers, discounted gym memberships, and health assessments
- Supportive and inclusive work environment focused on well-being and work-life balance
- Travel opportunities, with the chance to contribute to international clinical trials
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
- Minimum of 12 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience
- 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 and possess a valid driver's license
How to Stand Out (Preferred Qualifications):
- Experience in a fast-paced clinical environment
- Familiarity with data management systems and clinical trial software
- Previous involvement in diverse therapeutic areas and study types
#ClinicalResearch #ClinicalTrials #HealthcareCareers #DiversityAndInclusion #CareerGrowth
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