Clinical Site Associate

Reposted 2 Days Ago
Be an Early Applicant
tbilisi
In-Office
Junior
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
The Clinical Site Associate will support clinical trial operations by ensuring site compliance, managing communications, coordinating training, and maintaining documentation accuracy.
Summary Generated by Built In
CSA/ Clinical Site Associate

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

Job Advert Posting

Clinical Site Associate (CSA)

We are currently seeking a Clinical Site Associate (CSA) to join our diverse and dynamic team. As an CSA at ICON, you will play a pivotal role in supporting clinical trial operations by ensuring site compliance, documentation accuracy, and readiness for audits and inspections. This position involves close collaboration with Clinical Research Associates.

This role is office based in Georgia(Hybrid).

What you will be doing

Site Support & Oversight:

  • Manage site-level communications

  • Coordinate site trainings and systems access

  • Support site readiness activities including pre/post site visit tasks

  • Follow-up on action items

  • Document Management: Maintain Trial Master File (TMF)

Your profile

  • Bachelor's degree in a relevant field, such as life sciences or healthcare

  • Previous experience in clinical research or a related field preferred

  • Strong organizational and communication skills

  • Ability to work independently and collaboratively in a fast-paced environment

  • Attention to detail and ability to prioritize tasks effectively

#LI-TK1

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 maximize 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 site to read more about the benefits ICON offers.

At ICON, inclusion & 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 here.

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 here to apply

Top Skills

Clinical Trial Management
Communication Systems
Documentation Management
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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

What We Do

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

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