What are the responsibilities and job description for the Screening Coordinator position at ICON plc?
Screening Coordinator- Early Phase Clinical Research- ICON San Antonio TX
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Screening Coordinator to join our diverse and dynamic team. As a Screening Coordinator at ICON, you will play a crucial role in managing and overseeing the screening process for clinical trials, ensuring that participants are accurately evaluated and enrolled according to study protocols. You will contribute to the successful execution of trials by coordinating screening activities, liaising with study participants, and ensuring compliance with regulatory and study requirements.
Title: Screening Coordinator
Job Type: FT Permanent
Schedule: M-F 6 AM-230 PM
Location: 100% on site San Antonio TX
What You Will Be Doing
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. 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, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Screening Coordinator to join our diverse and dynamic team. As a Screening Coordinator at ICON, you will play a crucial role in managing and overseeing the screening process for clinical trials, ensuring that participants are accurately evaluated and enrolled according to study protocols. You will contribute to the successful execution of trials by coordinating screening activities, liaising with study participants, and ensuring compliance with regulatory and study requirements.
Title: Screening Coordinator
Job Type: FT Permanent
Schedule: M-F 6 AM-230 PM
Location: 100% on site San Antonio TX
What You Will Be Doing
- Managing the screening process for clinical trials, including participant recruitment, evaluation, and enrollment.
- Collaborating with cross-functional teams to ensure adherence to study protocols and regulatory guidelines.
- Overseeing the collection and management of screening data, ensuring accuracy and completeness.
- Providing support and guidance to participants throughout the screening process, addressing any questions or concerns they may have.
- Maintaining up-to-date knowledge of study protocols and regulatory requirements to ensure compliance and quality in screening activities.
- Bachelor’s degree in a relevant field such as life sciences, healthcare, or a related discipline.
- Experience in clinical research or healthcare settings, with a focus on participant screening and management.
- Strong organizational and communication skills, with the ability to manage multiple tasks and interact effectively with participants and team members.
- Attention to detail and proficiency in data management and documentation.
- Understanding of regulatory requirements and clinical trial protocols, with a commitment to maintaining high standards of compliance.
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. 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, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply
