Clinical Study Manager
- Company
- ICON Plc
- Location
- United States
- Salary
- Competitive
- Posted
- Sep 12, 2024
- Closes
- Sep 17, 2024
- Ref
- JR120429
- Discipline
- Clinical Research, Clinical Study Manager
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Clinical Study Manager - US, Lenexa, KS Office-based
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 Study Manager to join our diverse and dynamic team. As a Clinical Study Manager at ICON, you will play a pivotal role in overseeing and managing clinical studies, ensuring compliance with study protocols and regulatory requirements, and contributing to the advancement of innovative treatments and therapies through expert study management and leadership.
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:
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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 Study Manager to join our diverse and dynamic team. As a Clinical Study Manager at ICON, you will play a pivotal role in overseeing and managing clinical studies, ensuring compliance with study protocols and regulatory requirements, and contributing to the advancement of innovative treatments and therapies through expert study management and leadership.
What You Will Be Doing:
- Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines.
- Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies.
- Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans.
- Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies.
- Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle.
- Bachelor's degree in a relevant scientific discipline; advanced degree (Master’s or Ph.D.) is a plus.
- Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements.
- Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively.
- Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
- Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials.
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.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, 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