Clinical Research Associate
ICON, Atlanta, GA, United States
Clinical Research Associate (FSP - Sponsor dedicated)
What You Will Do
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolving queries to maintain high‑quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Your Profile
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent.
Minimum 1‑year relevant experience in clinical research site monitoring and management.
At least an intermediate level of English proficiency.
Experience in oncology therapeutics is a plus.
Knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
Good organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast‑paced environment.
Willingness to travel as required (approximately 60%).
What ICON can offer you
In addition to a competitive salary, we offer a range of benefits focused on well‑being and work‑life balance.
Various annual leave entitlements.
Health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings.
Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of professionals who 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.
We are committed to an inclusive and accessible environment. 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 have a medical condition or disability and require a reasonable accommodation for any part of the application process or to perform essential functions, please let us know or submit a request.
#J-18808-Ljbffr
What You Will Do
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Conducting site qualification, initiation, monitoring, and close‑out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolving queries to maintain high‑quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports.
Your Profile
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent.
Minimum 1‑year relevant experience in clinical research site monitoring and management.
At least an intermediate level of English proficiency.
Experience in oncology therapeutics is a plus.
Knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.
Good organizational and communication skills, with attention to detail.
Ability to work independently and collaboratively in a fast‑paced environment.
Willingness to travel as required (approximately 60%).
What ICON can offer you
In addition to a competitive salary, we offer a range of benefits focused on well‑being and work‑life balance.
Various annual leave entitlements.
Health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings.
Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of professionals who 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.
We are committed to an inclusive and accessible environment. 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 have a medical condition or disability and require a reasonable accommodation for any part of the application process or to perform essential functions, please let us know or submit a request.
#J-18808-Ljbffr