ICON Clinical Research
Clinical Research Associate - Miami, FL
ICON Clinical Research, New York, New York, United States
CRA 2, Miami, FL - Obesity Trials
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 Associate II in Miami, FL to support our client with Obesity trials to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
Conduct clinical trial site visits including evaluation, initiation, monitoring and close out
Oversee and report on the conduct of clinical trials at a site level including and on-line site visit reports and updates to electronic management systems
Proactive site management including:
Building and maintaining solid and professional relationships with site staff
Facilitating subject enrolment incorporating recruitment strategies and action plans at site level
Maintaining site audit/inspection readiness
Ensuring appropriate safety reporting and use of on-line safety reporting/reviewing systems
Verification of electronic case report form data against written and electronic source documentation as per study schema/monitoring plan
Responding to site queries and escalating issues in accordance with processes and timelines
Conducting IP accountability and reconciliation
Facilitating implementation of new technologies and systems at clinical sites (Electronic Data Capture, eSAE reporting)
Maintenance of site study supplies
Your profile
BA/BS/BSc in the sciences or nursing equivalent
A trained CRA with at least 2 years of on-site monitoring experience in phase II and phase III trials
Working knowledge of Electronic Data Capture (preferred)
Experience/working knowledge of the obesity trials experience (preferred)
Experience of Centralized/Risk Based/Targeted monitoring (preferred)
Experience of working within a metric based environment (preferred)
Comprehensive knowledge and understanding of ICH-GCP
Fluent oral (face to face and telephone) and written English language skills
Able and willing to travel up to 60% of the time or as per local requirements
Possession of a full driver’s license
Able and willing to work from a designated and appropriate home office as per local requirements
Willing to attend and contribute to team meetings including mandatory training (remote/off-site)
Competent computer skills including working knowledge of common software packages
Working knowledge of trial management databases and on-line systems
Able to attend a 1 week face to face in-house training course as part of on-boarding training
Able and willing to work on several protocols/therapy areas
What ICON can offer you:
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.
Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
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 (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) 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 Associate II in Miami, FL to support our client with Obesity trials to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
What you will be doing
Conduct clinical trial site visits including evaluation, initiation, monitoring and close out
Oversee and report on the conduct of clinical trials at a site level including and on-line site visit reports and updates to electronic management systems
Proactive site management including:
Building and maintaining solid and professional relationships with site staff
Facilitating subject enrolment incorporating recruitment strategies and action plans at site level
Maintaining site audit/inspection readiness
Ensuring appropriate safety reporting and use of on-line safety reporting/reviewing systems
Verification of electronic case report form data against written and electronic source documentation as per study schema/monitoring plan
Responding to site queries and escalating issues in accordance with processes and timelines
Conducting IP accountability and reconciliation
Facilitating implementation of new technologies and systems at clinical sites (Electronic Data Capture, eSAE reporting)
Maintenance of site study supplies
Your profile
BA/BS/BSc in the sciences or nursing equivalent
A trained CRA with at least 2 years of on-site monitoring experience in phase II and phase III trials
Working knowledge of Electronic Data Capture (preferred)
Experience/working knowledge of the obesity trials experience (preferred)
Experience of Centralized/Risk Based/Targeted monitoring (preferred)
Experience of working within a metric based environment (preferred)
Comprehensive knowledge and understanding of ICH-GCP
Fluent oral (face to face and telephone) and written English language skills
Able and willing to travel up to 60% of the time or as per local requirements
Possession of a full driver’s license
Able and willing to work from a designated and appropriate home office as per local requirements
Willing to attend and contribute to team meetings including mandatory training (remote/off-site)
Competent computer skills including working knowledge of common software packages
Working knowledge of trial management databases and on-line systems
Able to attend a 1 week face to face in-house training course as part of on-boarding training
Able and willing to work on several protocols/therapy areas
What ICON can offer you:
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.
Visit our careers site (https://careers.iconplc.com/benefits) to read more about the benefits ICON offers.
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 (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply