Clinical Research Associate - Central
ROLE DEFINITION & RESPONSIBILITIES
Role Overview
The Clinical Research Associate - Central role at ICON Strategic Solutions supports clinical trial operations and monitoring activities across assigned clinical programs. The position is responsible for conducting high-quality clinical monitoring, maintaining study documentation, coordinating study activities and collaborating with clinical investigators, site staff, sponsors and internal stakeholders. The client is seeking candidates with experience monitoring Ophthalmology trials or experience across multiple therapeutic areas.
Core Responsibilities
Patient Safety & Compliance
Required Qualifications
Therapeutic Area Preference
Experience monitoring Ophthalmology clinical trials or experience across multiple therapeutic areas is specifically sought by the client.
Benefits & Total Rewards
ICON states that employees receive competitive salaries and country-specific benefits focused on well-being and work-life balance. Listed benefits include annual leave, health-insurance options, retirement-planning offerings, a global Employee Assistance Programme, life assurance and flexible country-specific benefits such as childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes and health assessments, subject to applicable country eligibility.
Culture & Inclusion
ICON states that inclusion and belonging are fundamental to its culture and that it is committed to providing an accessible workplace free from discrimination and harassment. Qualified candidates are encouraged to apply even when they do not meet every listed requirement.
REQUIRED VERIFIED SKILLS
COMPENSATION & REWARDS
ORGANIZATION CONTEXT & CULTURE
ICON Strategic Solutions (FSP) / ICON plc is actively hiring for this position.
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.
