What are the responsibilities and job description for the Clinical Research Coordinator 2 position at Nextrials, Inc.?
Senior Clinical Research Coordinator- 100% on site Knoxville TN- Accellacare/ICON
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 Clinical Research Coordinator 2 (CRC) to join our diverse and dynamic team. As a CRC 2 at ICON Plc, you will play a pivotal role in coordinating and managing the day-to-day activities of clinical trials to ensure efficient execution and compliance with study protocols and regulatory standards. You will contribute to the success of clinical trials by overseeing site operations, participant management, and data collection processes.
100% Onsite role: Knoxville, TN
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 Clinical Research Coordinator 2 (CRC) to join our diverse and dynamic team. As a CRC 2 at ICON Plc, you will play a pivotal role in coordinating and managing the day-to-day activities of clinical trials to ensure efficient execution and compliance with study protocols and regulatory standards. You will contribute to the success of clinical trials by overseeing site operations, participant management, and data collection processes.
100% Onsite role: Knoxville, TN
What You Will Be Doing
- Coordinating and managing the operational aspects of clinical trials, including participant recruitment, scheduling, and site logistics.
- Ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards throughout the trial.
- Monitoring and documenting trial progress, including data collection, safety reporting, and regulatory compliance.
- Providing training and support to site staff to ensure the effective execution of trial procedures and protocols.
- Building and maintaining strong relationships with study participants and site personnel to facilitate smooth trial operations and address any issues that arise.
- Degree in a relevant field such as life sciences or healthcare management.
- 3 years of extensive experience as a Clinical Research Coordinator, with a comprehensive understanding of clinical trial processes and regulatory requirements.
- Strong organizational and multitasking skills, with the ability to manage multiple aspects of clinical trials simultaneously.
- Proficiency in clinical trial software and tools, with a keen eye for detail and accuracy in data management and documentation.
- Excellent communication, interpersonal, and problem-solving skills, with the ability to work effectively with a diverse team and drive successful trial outcomes.
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
