Clinical Trial Assistance
Nextrials, Inc., Whitpain Hills, PA, United States
Clinical Trial Assistant
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.
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities
Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
Collaborate with cross‑functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
Support study close‑out activities including data cleaning, analysis, and preparation of clinical study reports.
Your Profile
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required Qualifications & Experience
Bachelor’s degree in a relevant scientific discipline or healthcare‑related field
Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
Strong organizational and time‑management skills, with the ability to prioritize tasks and manage competing priorities effectively
Excellent attention to detail and problem‑solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance
Effective communication and interpersonal skills, with the ability to collaborate cross‑functionally and build strong relationships with study teams and clinical sites
Willingness to travel as required (approximately 60%)
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 designed to be competitive within each country and focused on well‑being and work‑life balance for you and your family.
Our Benefits Examples
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
Equal Opportunity Statement
At ICON, inclusion & belonging are fundamental to our culture and values. We are 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 you need a reasonable accommodation for any part of the application process or to perform essential functions because of a medical condition or disability, please let us know or submit a request.
#J-18808-Ljbffr
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.
As a Clinical Associate at ICON, you will support the design, implementation, and management of clinical trials, contributing to the advancement of innovative treatments and therapies.
What You Will Do
You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.
Key Responsibilities
Assist in the planning, execution, and monitoring of clinical trials, ensuring adherence to protocol requirements, regulatory guidelines, and industry standards.
Coordinate study activities including site initiation, patient recruitment, data collection, and monitoring visits to ensure timely and accurate data collection and documentation.
Collaborate with cross‑functional teams including Clinical Operations, Data Management, and Biometrics to support the successful execution of clinical trials.
Maintain comprehensive study documentation and records, ensuring compliance with applicable regulations and standard operating procedures.
Support study close‑out activities including data cleaning, analysis, and preparation of clinical study reports.
Your Profile
You will bring relevant clinical coordination experience, along with the following qualifications and skills.
Required Qualifications & Experience
Bachelor’s degree in a relevant scientific discipline or healthcare‑related field
Previous experience in clinical research or healthcare, preferably within the pharmaceutical, biotechnology, or CRO industry
Strong organizational and time‑management skills, with the ability to prioritize tasks and manage competing priorities effectively
Excellent attention to detail and problem‑solving abilities, with a commitment to ensuring data accuracy, integrity, and compliance
Effective communication and interpersonal skills, with the ability to collaborate cross‑functionally and build strong relationships with study teams and clinical sites
Willingness to travel as required (approximately 60%)
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 designed to be competitive within each country and focused on well‑being and work‑life balance for you and your family.
Our Benefits Examples
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
Equal Opportunity Statement
At ICON, inclusion & belonging are fundamental to our culture and values. We are 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 you need a reasonable accommodation for any part of the application process or to perform essential functions because of a medical condition or disability, please let us know or submit a request.
#J-18808-Ljbffr