Study Delivery Specialist
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Job Description
Site Management Associate I at ICON supporting clinical trial management and site monitoring activities for a global healthcare organisation. Delivering clinical research work and collaborating with cross-functional teams.
Responsibilities:
- Delivering clinical research work to a high standard, working closely with your team and stakeholders.
- Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics.
- Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively.
- Maintaining accurate records of site activities and contributing to the preparation of monitoring reports.
- Participating in training and development initiatives to enhance knowledge and skills in clinical trial management.
Requirements:
- Bachelor's degree in a relevant field such as life sciences, healthcare administration, or clinical research.
- Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory.
- Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively.
- Basic knowledge of clinical trial processes and regulatory requirements is a plus.
- Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.
- Willingness to travel as required (approximately 25%)
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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