Clinical Research Associate - Oncology - Midwest (Field Based)

Overview

As a Clinical Research Associate you will be joining the worlds largest & most comprehensive clinical research organization, powered by healthcare intelligence.

Responsibilities

• Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and Internation Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines.
• Assesses the qualification of potential investigative sites, initiates clinical trials at investigative sites, instructs site personnel on the proper conduct of clinical trials, and closes clinical trials at investigative sites.
• Responsible for site startup activities for assigned sites, including but not limited to regulatory documents collection, informed consent review, IRB / IEC submission support, and budgets and contracts negotiations.
• Reviews and verifies accuracy of clinical trial data collected, either onsite or remotely
• Provides regular site status information to team members, trial management, and updates trial management tools.
• Completes monitoring activity documents as required by sponsor's SOPs.
• Works closely with other clinical team members to facilitate timely resolution of trial and / or clinical issues.
• Escalates site and trial related issues per Sponsor's SOPs until identified issues are resolved or closed.
• Performs essential document site file reconciliation.
• Performs source document verification and query resolution.
• Assesses investigational product (IP) accountability, dispensation, and compliance at the investigative sites.
• Verifies serious adverse event (SAE) reporting according to trial specifications and ICH GCP guidelines.
• Communicates with investigative sites.
• Updates applicable tracking systems
• Ensures all required training is completed and documented.
• May be assigned to complex studies and / or sites.
• Provides leadership skills to assigned projects within the clinical operations department.

Qualifications

Pay Range ($91,336.00 / Yr.USD - 114,170.00 / Yr USD)

Actual compensation will be determined based on factors such as geographic location, work experience, education / training, and skill level.

What ICON can offer you

Our success depends on the quality of our people. Thats why weve 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 :

Visit our careers website to read more about the benefits of working at ICON :

Equal Employment Opportunity Statement

At ICON, inclusion & belonging are fundamental to our culture and values. Were 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, 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 through the form below.

Interested in the role, but unsure if you meet all of the requirements?

We would encourage you to apply regardless theres every chance youre exactly what were looking for here at ICON whether it is for this or other roles.

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