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Job Description
- Req#: 118322
Employer Industry: Clinical Research Organization
Why consider this job opportunity:
- Competitive salary with a range of additional benefits focused on well-being and work-life balance
- Opportunity for career advancement and growth within a diverse and inclusive organization
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, and discounted gym memberships
- Access to a Global Employee Assistance Programme providing 24-hour support for you and your family
- Various annual leave entitlements to support work-life balance
What to Expect (Job Responsibilities):
- Manage day-to-day assigned study responsibilities to ensure deliverables are met in all phases of the trial
- Contribute to the development of study documents, including drafting updates and managing reviews
- Assist with clinical development strategy, budget management, and study-level timelines
- Oversee assigned CRO activities and manage budgets and contracts for clinical sites
- Support clinical trial processes including monitoring oversight and managing clinical quality metrics
What is Required (Qualifications):
- At least 2 years of trial coordination experience in a clinical research environment, with up to 5 years in the industry
- Bachelor’s degree in a science-based subject; advanced degree preferred
- Solid understanding of drug development and FDA/ICH GCP guidelines
- Excellent verbal and written communication skills
- Strong organizational skills and attention to detail
How to Stand Out (Preferred Qualifications):
- Experience in a global setting within the clinical research industry
- Good project management skills
#ClinicalResearch #CareerOpportunity #InclusiveWorkplace #ProjectManagement #ClinicalTrials
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