Clinical Trial Associate – Magazica Career Hub

Title: Clinical Trial Associate

Company: ICON
Location: Burlington, Ontario
Job Type: FlexTime, FullTime

Description:

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Clinical Trial Associate (CTA) to join their team. The CTA will oversee site management activities, ensuring compliance with study protocols, regulatory requirements, and timelines. Responsibilities include collaborating with site staff and cross-functional teams, assisting with site initiation and close-out activities, providing guidance to junior staff, and maintaining site management documentation.

Key Responsibilities:

Overseeing day-to-day site management activities

Collaborating with site staff and cross-functional teams

Assisting with site initiation, monitoring visits, and close-out activities

Providing guidance and mentorship to junior staff

Preparing and maintaining site management documentation

Qualifications:

Bachelor's degree in life sciences, clinical research, or related field

Extensive experience in site management or clinical operations

Strong understanding of clinical trial processes and regulatory requirements

Excellent problem-solving and organizational skills

Effective communication and interpersonal skills

ICON offers competitive benefits including various annual leave entitlements, health insurance, retirement planning, and a Global Employee Assistance Programme. They are committed to creating an inclusive and accessible workplace free of discrimination and harassment. Candidates are encouraged to apply even if they do not meet all requirements, as ICON values diversity and talent. Interested candidates can apply through the provided link.

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Title: Clinical Trial Associate
Company: ICON
Location: Burlington, Ontario
Clinical Trial AssociateICON plc is a worldleading 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 developmentWe are currently seeking a CTA to join our diverse and dynamic team. As a CTA at ICON, you will play a critical role in overseeing site management activities, ensuring the smooth operation of clinical trials at the site level. You will work closely with clinical teams, providing guidance and support to ensure that sites meet regulatory and operational requirements while delivering highquality data and achieving study goals.What You Will Be Doing: Overseeing daytoday site management activities, ensuring that clinical trial sites comply with study protocols, regulatory requirements, and timelines.Collaborating with site staff and crossfunctional teams to resolve issues, monitor progress, and ensure timely data collection and reporting.Assisting with site initiation, monitoring visits, and closeout activities to ensure the proper execution of clinical trials.Providing guidance and mentorship to junior site management staff, fostering collaboration and process improvement.Preparing and maintaining site management documentation, including site reports, communications, and updates on site performance.Your Profile: Bachelor's degree in life sciences, clinical research, or a related field.Extensive experience in site management, clinical operations, or monitoring within the clinical research industry.Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements.Excellent problemsolving and organizational skills, with the ability to manage multiple sites and timelines.Effective communication and interpersonal skills, with a focus on collaboration and maintaining strong site relationships.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 wellbeing and work life balance opportunities for you and your family.Our benefits examples include:Various annual leave entitlementsA 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, TELUS Health, offering 24hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's wellbeing.Life assuranceFlexible countryspecific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.Visit our to read more about the benefits ICON offers.At ICON, inclusion &amp; 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 .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 to apply

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