Study Delivery Specialist
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Job Description
Study Delivery Specialist supporting clinical trial site monitoring for ICON, a global clinical research organization. Ensuring protocol compliance, site documentation, performance tracking, and monitoring reports.
Responsibilities:
- Assist in monitoring clinical trial sites
- Ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines
- Support site management activities, including documentation preparation, data entry, and tracking site performance metrics
- Collaborate with cross-functional teams to facilitate communication and address site-related issues
- Maintain accurate records of site activities
- Contribute to the preparation of monitoring reports
- Participate 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
- 1–2 years of experience in global study delivery clinical research and site management
- Strong organizational skills and attention to detail
- Ability to manage multiple tasks effectively
- Very strong knowledge of clinical trial processes and regulatory requirements
- Excellent communication and interpersonal skills
- Ability to work collaboratively within a team environment
- Willingness to travel as required, approximately 25%
- Legal right to work in the country where the role is based
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
- Inclusive and accessible workplace
- Reasonable accommodations during the recruitment process
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