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Job Description
- Req#: 113496
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Competitive salary with a range of additional benefits
- Various annual leave entitlements for work-life balance
- Comprehensive health insurance offerings for you and your family
- Global Employee Assistance Programme providing 24-hour access to a network of specialized professionals
- Opportunities for career advancement in a diverse and inclusive environment
- Flexible country-specific optional benefits tailored to your needs
What to Expect (Job Responsibilities):
- Participate in study planning and set-up activities, including vendor management and project coordination
- Monitor the execution of clinical study deliverables against specified timelines and budgets
- Coordinate the preparation and conduct of site initiations and investigator meetings
- Manage the planning and procurement of ancillary clinical supplies and collaborate with relevant teams
- Support and oversee vendor activities and maintain communication with the study team
What is Required (Qualifications):
- Detailed knowledge of ICH, GCP, FDA regulations, and applicable international guidelines
- Experience interacting with external vendors, such as CROs and labs
- Understanding of the drug development process and procedures
- Strong organization, planning, and communication skills
- BA/BS/BSc in the sciences or RN qualification
How to Stand Out (Preferred Qualifications):
- Familiarity with advanced concepts of clinical research
- Advanced computer skills and ability to understand technical and scientific information
- Experience with the development of prospective site selection criteria
- Previous experience in clinical study management or related roles
#ClinicalResearch #HealthcareJobs #CareerOpportunities #DiversityAndInclusion #ClinicalDevelopment
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