Employer Industry: Clinical Research Organization

Why consider this job opportunity:
- Competitive salary and a range of health insurance offerings to suit you and your family’s needs
- Various annual leave entitlements and competitive retirement planning offerings
- Global Employee Assistance Programme providing 24-hour access to a network of specialized professionals
- Flexible country-specific optional benefits, including childcare vouchers and discounted gym memberships
- Opportunity to work within a diverse culture that rewards high performance and nurtures talent
- Chance to contribute to innovative clinical research that serves patients and communities

What to Expect (Job Responsibilities):
- Work with clinical study teams to ensure the accuracy of data in Clinical Trial Management Systems (CTMS)
- Conduct research and data analysis to identify potential sites that meet study criteria and objectives
- Assist with feasibility launches, including system set-up and site-level feasibility questionnaire outreach
- Communicate effectively with study teams and stakeholders to support additional feasibility activities
- Troubleshoot issues or discrepancies that arise during the feasibility process

What is Required (Qualifications):
- B.S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience in clinical trial conduct and processes, or 2+ years in feasibility/recruitment
- Experience with trial optimization vendors, tools, and methods
- Strong analytical skills with great attention to detail
- Good knowledge of clinical research concepts and drug development
- Excellent written and verbal communication skills

How to Stand Out (Preferred Qualifications):
- Experience collaborating with internal and external stakeholders
- Demonstrated administrative and project management abilities in an academic, CRO, or sponsor environment
- Ability to prioritize multiple projects and tasks within tight timelines

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