Clinical Associate - CTA

ICON plc is a premier global healthcare intelligence and clinical research organization committed to fostering an inclusive environment that drives innovation and excellence. We are dedicated to shaping the future of clinical development and invite you to join our mission.

As a Clinical Associate (CTA) at ICON, you will play a crucial role in supporting the design, implementation, and management of clinical trials. Your contributions will be vital in advancing innovative treatments and therapies.

• Assist in the comprehensive planning, execution, and ongoing monitoring of clinical trials, ensuring strict adherence to protocol requirements, regulatory guidelines, and industry best practices.
• Coordinate essential study activities, including site initiation, patient recruitment, meticulous data collection, and conducting monitoring visits to guarantee timely and accurate data capture and documentation.
• Engage in collaborative efforts with diverse cross-functional teams, such as Clinical Operations, Data Management, and Biometrics, to ensure the successful progression of clinical trials.
• Maintain thorough and organized study documentation and records, ensuring full compliance with all applicable regulations and standard operating procedures.
• Support the completion of study close-out activities, which include data verification, analysis, and the preparation of detailed clinical study reports.

We are seeking individuals with relevant clinical coordination experience, complemented by the following qualifications and skills:

• Possession of a Bachelor's degree in a pertinent scientific discipline or a healthcare-related field.
• Prior experience in clinical research or the healthcare sector, ideally within the pharmaceutical, biotechnology, or Contract Research Organization (CRO) industry.
• Demonstrated strong organizational and time management capabilities, with a proven ability to prioritize tasks effectively and manage multiple competing demands.
• Exceptional attention to detail and robust problem-solving skills, coupled with a commitment to ensuring data accuracy, integrity, and regulatory compliance.
• Effective communication and interpersonal skills, enabling successful collaboration with cross-functional teams and the establishment of strong relationships with study personnel and clinical sites.
• A willingness to travel as required for the role.

Our success is driven by the caliber of our people. Consequently, we prioritize cultivating a diverse culture that recognizes high performance and supports talent development. In addition to a competitive salary, ICON provides a comprehensive suite of benefits designed to be competitive globally and focused on well-being and work-life balance for you and your family. Benefits may include various annual leave entitlements, extensive health insurance options, competitive retirement planning, a Global Employee Assistance Programme (LifeWorks) offering 24-hour support, life assurance, and flexible country-specific optional benefits such as childcare vouchers, bike purchase schemes, and discounted gym memberships.

At ICON, inclusion and belonging are fundamental to our culture and values. We are committed to providing an inclusive and accessible environment for all candidates. ICON upholds a workplace free from discrimination and harassment, offering equal employment consideration to all qualified applicants regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. If you require reasonable accommodation due to a medical condition or disability during the application process or to perform essential job functions, please inform us or submit a request. We encourage individuals who may not meet every listed requirement to apply, as your unique qualifications might be exactly what we are looking for, whether for this role or others.