Clinical Associate
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Job Description
Clinical Associate at ICON supports execution and management of clinical trials. Contributing to advancement of innovative treatments and therapies in a fast-paced environment.
Responsibilities:
- Support clinical trial deliverables, applying skills to ensure quality and efficiency
- Independently support the planning, execution, and reporting of clinical trials across all phases and therapeutic areas
- Maintain and analyze trial tracking systems, ensuring data accuracy and compliance
- Track and analyze trial budgets, including actual vs. planned spend, and follow up on variances
- Manage the Trial Master File (TMF), ensuring completeness and inspection readiness
- Oversee investigational product (IP) and ancillary supply management, including ordering, distribution, and tracking
- Coordinate site and country feasibility assessments and regulatory documentation processes
- Prepare and analyze key clinical trial data reports and metrics
Requirements:
- Bachelor's degree in a relevant field, such as life sciences or healthcare preferred
- Previous experience in clinical research or a related field preferred
- Strong organizational and communication skills
- Ability to work independently and collaboratively in a fast-paced environment
- Attention to detail and ability to prioritize tasks effectively
Benefits:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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