Description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a Trial Master File (TMF) Specialist I at ICON, you will become familiar with Trial Master File (TMF) documentation and document management activities.
Your role will involve delivering trial master file management work to a high standard, working closely with your team and stakeholders. Key responsibilities include:
- Gain familiarity with Trial Master File (TMF) documentation and document management processes
- Contribute to client services contracts and internal ICON business needs related to TMF management
- Ensure compliance with client requirements and ICON procedures
- Assist in the maintenance and organization of TMF documentation
- Collaborate with cross-functional teams to ensure timely and accurate documentation filing
You will bring relevant trial master file management experience, along with the following qualifications and skills. Required qualifications and experience:
- Bachelor's degree in a relevant field
- Prior experience in clinical research or document management preferred
- Strong attention to detail and organizational skills
- Ability to work effectively in a team environment
- Excellent communication skills
- Willingness to travel as required (approximately 5%)
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- 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