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Job Description
- Req#: JR140073
Employer Industry: Clinical Research and Healthcare
Why consider this job opportunity:
- Competitive salary with various annual leave entitlements
- Comprehensive health insurance offerings to suit you and your family's needs
- Competitive retirement planning options to maximize savings
- Global Employee Assistance Programme providing 24-hour access to specialized professionals for well-being support
- Flexible benefits including childcare vouchers, discounted gym memberships, and more
- Opportunity to work in a diverse and inclusive culture that fosters talent and high performance
What to Expect (Job Responsibilities):
- Monitor clinical trial sites to ensure compliance with study protocols and regulatory requirements
- Conduct site visits to assess performance, resolve issues, and provide necessary support
- Collaborate with cross-functional teams for timely and accurate data collection and reporting
- Provide training and guidance to site staff and other Clinical Research Associates (CRAs)
- Build and maintain effective relationships with site personnel and stakeholders to facilitate trial operations
What is Required (Qualifications):
- Advanced degree in a relevant field such as life sciences, nursing, or medicine
- Extensive experience as a Clinical Research Associate with a strong understanding of clinical trial processes
- Proven ability to manage multiple sites and projects simultaneously
- Expertise in monitoring practices, data integrity, and site management
- Ability to travel at least 60% of the time and possess a valid driver's license
How to Stand Out (Preferred Qualifications):
- Strong organizational and problem-solving skills
- Excellent communication, interpersonal, and stakeholder management skills
- Proficiency in relevant clinical trial software and tools
#ClinicalResearch #Oncology #HealthcareCareers #DiversityAndInclusion #ClinicalTrials
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