Clinical Trial Assistant
Posted on Sep 15, 2024 by Pharmaceutical Research Associates, Inc
Emelle, AL
Research
Immediate Start
Annual Salary
Full-Time
Overview:
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.
Eager to explore your first steps into clinical research? Eager to become part of the development of a medicine?
In the function of Clinical Trial Assistant (CTA) you are able to place your first steps in clinical trials. You will learn everything on how a study is conducted, what paperwork is required, how data are being collected, analysed and tracked, and so much more.
This position offers you to enter clinical research and opens the doors for further career opportunities!
As a CTA within our single-sponsor model, you will be working for a leading pharmaceutical company, with offices in the Vilvoorde region.
A perfect opportunity to put a reputated pharma on your RESUME!
Responsibilities:
Purpose
You will provide support (administrative, logistic and document management) in the preparation and execution of all study related activities within agreed timelines.
Major accountabilities
Specialists responsible for administrative management of trials (In collaboration with CSMs and CRAs, responsible to set-up and keep country and site TMFs continuously up to date according to regulatory and requirements.)
Responsible for the preparation, tracking, processing of all study related documentation and material
Manages logistics and document exchange between clinical sites and our company
Updates clinical study management systems
Works in continuous collaboration with other associates/team members
Applies company policies and procedures to resolve routine issues.
Contacts are primarily with immediate supervisor and other personnel in department or group
Works on problems of routine scope. Follows established policies and procedures.
Normally receives detailed instructions on all work
Clinical Trial Supplies
Assists local trial team with the creation, ordering, and mailing of any study tools including recruitment materials as well as newsletters, email communications, faxes, etc.
Supports local trial team with ordering/tracking/mailing of any necessary trials supplies including the regulatory binder, lab kits.
Support the CSM with the coordination of internal and external suppliers, including customs, to ensure import of all clinical trial supplies (including drug supply)
Coordinate shipment of clinical trial supplies to local sites
Co-ordinate relabeling of IMP at warehouse when needed.
Finance
Track, process and release payments to vendors in collaboration with local study team and finance.
Qualifications:
A degree or equivalent in a scientific of health care discipline. Equivalent by experience is also considered!
Fluent communication skills in Dutch, English, and French
Managing multiple priorities and computer literacy
Excellent interpersonal skills with demonstrated good expertise in teamwork
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 maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: (url removed)
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, 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 .
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.
#LI-Hybrid
#LI-VV1
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.
Eager to explore your first steps into clinical research? Eager to become part of the development of a medicine?
In the function of Clinical Trial Assistant (CTA) you are able to place your first steps in clinical trials. You will learn everything on how a study is conducted, what paperwork is required, how data are being collected, analysed and tracked, and so much more.
This position offers you to enter clinical research and opens the doors for further career opportunities!
As a CTA within our single-sponsor model, you will be working for a leading pharmaceutical company, with offices in the Vilvoorde region.
A perfect opportunity to put a reputated pharma on your RESUME!
Responsibilities:
Purpose
You will provide support (administrative, logistic and document management) in the preparation and execution of all study related activities within agreed timelines.
Major accountabilities
Specialists responsible for administrative management of trials (In collaboration with CSMs and CRAs, responsible to set-up and keep country and site TMFs continuously up to date according to regulatory and requirements.)
Responsible for the preparation, tracking, processing of all study related documentation and material
Manages logistics and document exchange between clinical sites and our company
Updates clinical study management systems
Works in continuous collaboration with other associates/team members
Applies company policies and procedures to resolve routine issues.
Contacts are primarily with immediate supervisor and other personnel in department or group
Works on problems of routine scope. Follows established policies and procedures.
Normally receives detailed instructions on all work
Clinical Trial Supplies
Assists local trial team with the creation, ordering, and mailing of any study tools including recruitment materials as well as newsletters, email communications, faxes, etc.
Supports local trial team with ordering/tracking/mailing of any necessary trials supplies including the regulatory binder, lab kits.
Support the CSM with the coordination of internal and external suppliers, including customs, to ensure import of all clinical trial supplies (including drug supply)
Coordinate shipment of clinical trial supplies to local sites
Co-ordinate relabeling of IMP at warehouse when needed.
Finance
Track, process and release payments to vendors in collaboration with local study team and finance.
Qualifications:
A degree or equivalent in a scientific of health care discipline. Equivalent by experience is also considered!
Fluent communication skills in Dutch, English, and French
Managing multiple priorities and computer literacy
Excellent interpersonal skills with demonstrated good expertise in teamwork
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 maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: (url removed)
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, 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 .
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.
#LI-Hybrid
#LI-VV1
Reference: 200050112
https://jobs.careeraddict.com/post/95263395
Clinical Trial Assistant
Posted on Sep 15, 2024 by Pharmaceutical Research Associates, Inc
Emelle, AL
Research
Immediate Start
Annual Salary
Full-Time
Overview:
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.
Eager to explore your first steps into clinical research? Eager to become part of the development of a medicine?
In the function of Clinical Trial Assistant (CTA) you are able to place your first steps in clinical trials. You will learn everything on how a study is conducted, what paperwork is required, how data are being collected, analysed and tracked, and so much more.
This position offers you to enter clinical research and opens the doors for further career opportunities!
As a CTA within our single-sponsor model, you will be working for a leading pharmaceutical company, with offices in the Vilvoorde region.
A perfect opportunity to put a reputated pharma on your RESUME!
Responsibilities:
Purpose
You will provide support (administrative, logistic and document management) in the preparation and execution of all study related activities within agreed timelines.
Major accountabilities
Specialists responsible for administrative management of trials (In collaboration with CSMs and CRAs, responsible to set-up and keep country and site TMFs continuously up to date according to regulatory and requirements.)
Responsible for the preparation, tracking, processing of all study related documentation and material
Manages logistics and document exchange between clinical sites and our company
Updates clinical study management systems
Works in continuous collaboration with other associates/team members
Applies company policies and procedures to resolve routine issues.
Contacts are primarily with immediate supervisor and other personnel in department or group
Works on problems of routine scope. Follows established policies and procedures.
Normally receives detailed instructions on all work
Clinical Trial Supplies
Assists local trial team with the creation, ordering, and mailing of any study tools including recruitment materials as well as newsletters, email communications, faxes, etc.
Supports local trial team with ordering/tracking/mailing of any necessary trials supplies including the regulatory binder, lab kits.
Support the CSM with the coordination of internal and external suppliers, including customs, to ensure import of all clinical trial supplies (including drug supply)
Coordinate shipment of clinical trial supplies to local sites
Co-ordinate relabeling of IMP at warehouse when needed.
Finance
Track, process and release payments to vendors in collaboration with local study team and finance.
Qualifications:
A degree or equivalent in a scientific of health care discipline. Equivalent by experience is also considered!
Fluent communication skills in Dutch, English, and French
Managing multiple priorities and computer literacy
Excellent interpersonal skills with demonstrated good expertise in teamwork
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 maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: (url removed)
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, 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 .
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.
#LI-Hybrid
#LI-VV1
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.
Eager to explore your first steps into clinical research? Eager to become part of the development of a medicine?
In the function of Clinical Trial Assistant (CTA) you are able to place your first steps in clinical trials. You will learn everything on how a study is conducted, what paperwork is required, how data are being collected, analysed and tracked, and so much more.
This position offers you to enter clinical research and opens the doors for further career opportunities!
As a CTA within our single-sponsor model, you will be working for a leading pharmaceutical company, with offices in the Vilvoorde region.
A perfect opportunity to put a reputated pharma on your RESUME!
Responsibilities:
Purpose
You will provide support (administrative, logistic and document management) in the preparation and execution of all study related activities within agreed timelines.
Major accountabilities
Specialists responsible for administrative management of trials (In collaboration with CSMs and CRAs, responsible to set-up and keep country and site TMFs continuously up to date according to regulatory and requirements.)
Responsible for the preparation, tracking, processing of all study related documentation and material
Manages logistics and document exchange between clinical sites and our company
Updates clinical study management systems
Works in continuous collaboration with other associates/team members
Applies company policies and procedures to resolve routine issues.
Contacts are primarily with immediate supervisor and other personnel in department or group
Works on problems of routine scope. Follows established policies and procedures.
Normally receives detailed instructions on all work
Clinical Trial Supplies
Assists local trial team with the creation, ordering, and mailing of any study tools including recruitment materials as well as newsletters, email communications, faxes, etc.
Supports local trial team with ordering/tracking/mailing of any necessary trials supplies including the regulatory binder, lab kits.
Support the CSM with the coordination of internal and external suppliers, including customs, to ensure import of all clinical trial supplies (including drug supply)
Coordinate shipment of clinical trial supplies to local sites
Co-ordinate relabeling of IMP at warehouse when needed.
Finance
Track, process and release payments to vendors in collaboration with local study team and finance.
Qualifications:
A degree or equivalent in a scientific of health care discipline. Equivalent by experience is also considered!
Fluent communication skills in Dutch, English, and French
Managing multiple priorities and computer literacy
Excellent interpersonal skills with demonstrated good expertise in teamwork
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 maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: (url removed)
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, 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 .
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.
#LI-Hybrid
#LI-VV1
Reference: 200050112
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