Description
As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.
Key responsibilities include:
- Bachelor's/ Master's degree in life sciences or a related field
- Previous experience in clinical research, site management, or a related field preferred (i.e. right from Pre-Trials Assessment to Close outs)
- Min. 2 years experience in Project Management or Clinical Trial Management in an MNC
- Min 8+ years in Onsite monitoring experience with 5+ years in MNC
- Should be responsible for complete Site Management
- Should have SEC (Subject Expert Committee) presentation Skills to Regulatory Authorities (Preferred)
- Strong interpersonal and communication skills, with the ability to build rapport and establish effective working relationships with diverse stakeholders
- Excellent organisational and problem-solving skills, with the ability to prioritise and manage multiple tasks simultaneously
- Knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials
- Willingness to travel as required (approximately 60%)
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