ICON Strategic Solutions
Sr. CRA - Central US - Oncology
ICON Strategic Solutions, Chicago, Illinois, United States, 60290
Sr. CRA – Central US – Oncology
Join ICON Strategic Solutions, a world‑leading healthcare intelligence and clinical research organization, to become our next Senior Clinical Research Associate in the Central US Oncology team.
As a Senior CRA, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements and industry standards. Your work will support data integrity, participant safety and compliance throughout the study lifecycle.
What You Will Be Doing
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues and provide support to ensure successful trial execution.
Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile
Advanced degree in a relevant field such as life sciences, nursing or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
Expertise in monitoring practices, data integrity and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in Central US near a major airport.
Five years of CRA experience with oncology monitoring experience.
Ability to travel at least 60% of the time (international and domestic – fly and drive) and possessing a valid driver’s license.
What ICON Can Offer You In addition to a competitive salary, ICON offers a range of benefits that focus on well‑being and work‑life balance.
Benefits Examples Include
Various annual leave entitlements.
Health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings.
Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialised professionals.
Life assurance.
Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, subsidised travel passes, health assessments, and more.
Equal Employment Opportunity At ICON, inclusion and belonging are fundamental to our culture and values. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If you need a reasonable accommodation for any part of the application process or to perform the essential functions of this position because of a medical condition or disability, please let us know or submit a request here.
#J-18808-Ljbffr
As a Senior CRA, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements and industry standards. Your work will support data integrity, participant safety and compliance throughout the study lifecycle.
What You Will Be Doing
Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements and Good Clinical Practice (GCP) standards.
Conducting site visits to assess site performance, resolve issues and provide support to ensure successful trial execution.
Collaborating with cross‑functional teams to ensure timely and accurate data collection and reporting.
Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Your Profile
Advanced degree in a relevant field such as life sciences, nursing or medicine.
Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem‑solving skills.
Expertise in monitoring practices, data integrity and site management, with proficiency in relevant clinical trial software and tools.
Excellent communication, interpersonal and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Must be located in Central US near a major airport.
Five years of CRA experience with oncology monitoring experience.
Ability to travel at least 60% of the time (international and domestic – fly and drive) and possessing a valid driver’s license.
What ICON Can Offer You In addition to a competitive salary, ICON offers a range of benefits that focus on well‑being and work‑life balance.
Benefits Examples Include
Various annual leave entitlements.
Health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings.
Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialised professionals.
Life assurance.
Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, subsidised travel passes, health assessments, and more.
Equal Employment Opportunity At ICON, inclusion and belonging are fundamental to our culture and values. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If you need a reasonable accommodation for any part of the application process or to perform the essential functions of this position because of a medical condition or disability, please let us know or submit a request here.
#J-18808-Ljbffr