JUMP TO CONTENT

CTA

  1. Mexico City
2025-116290
  1. Study Start Up
  2. ICON Strategic Solutions

About the role

This vacancy has now expired. Please click here to view live vacancies.

As a CTA  you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


What you will be doing:

CTA assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team to ensure quality and consistency of interventional study deliverables to time, cost and quality objectives

  • Collects, assists in preparation, reviews and tracks documents for the application process as well as coordination and tracking of study materials and equipment
  • Assist in submission of proper application/documents to EC/IRB and, where appropriate to Regulatory Authorities
  • Interfaces with Investigators, external service providers and CRAs during the document collection process
  • Local administrative main contact and works closely with the CRAs and/or the LSAD for the duration of the study
  • Set-up and maintenance of the local eTMF and ISF including document tracking in accordance with ICH-GCP and local requirements
  • Ensures essential documents are uploaded in a timely manner to maintain the eTMF “Inspection Readiness” and study documents are ready for final archiving and completion of local part of the eTMF and supports the CRA in the close out activities for the ISF
  • Prepares and/or supports contract preparation at a site level (with the exception of countries where there is a specific role dedicated to preparing site contracts)
  • Leads the practical arrangements and contributes to the preparation of internal and external meetings. Responsible for printing and distribution of documents such as letters and meeting minutes, and for handling and archiving of study/country related e-mails
  • Interfaces with Data Management Centre and/or Data Management, Global Clinical Solutions representatives to facilitate the delivery of study related documents/material
  • Ensures compliance with local, national and regional legislation, as applicable

You are:

  • Bachelor/ Master degree
  • At least two years of experience as Study Coordinator or any other administrative position within Pharmaceutical Industry
  • Excellent planning/ organizational skills
  • Problem solving attitude
  • Strong team player


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 maximise 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 website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. 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 through the form below.

https://careers.iconplc.com/reasonable-accommodations

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.

List #1

Day in the life

Similar jobs at ICON

Site Specialist II

Salary

Location

Turkey, Ankara

Location

Ankara

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

What you will be doingLeading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.Coordina

Reference

JR139810

Expiry date

01/01/0001

Jacek Jaworski Read more Shortlist Save this role
Study Start Up Associate I - German speaker

Salary

Location

Bulgaria, Sofia

Location

Sofia

Prague

Budapest

Warsaw

Johannesburg

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clin

Reference

JR137116

Expiry date

01/01/0001

Jacek Jaworski Read more Shortlist Save this role
Site Specialist I

Salary

Location

China, Chengdu

Location

Chengdu

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

TBC

Reference

JR135261

Expiry date

01/01/0001

Allen Hao

Author

Allen Hao
Allen Hao

Author

Allen Hao
Read more Shortlist Save this role
Site Specialist I

Salary

Location

China, Beijing

Location

Beijing

Chengdu

Guangzhou

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

TBC

Reference

JR137575

Expiry date

01/01/0001

Allen Hao

Author

Allen Hao
Allen Hao

Author

Allen Hao
Read more Shortlist Save this role
Director, FSA

Salary

Location

Japan, Osaka

Location

Osaka

Tokyo

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Study Start Up

Job Type

Permanent

Description

当社では、IPH・IBT・ICO の Site Activation 業務を横断的に統合し、日本の臨床試験環境の変革を推進するための FSA(Feasibility / Site Activation)ディレクター を募集しています。■ポジション概要 本ポジションは、各部門に分散していた Feasibility / Site Activation 機能を統合し、最適なプロセス設計、効率的なリソース

Reference

JR133204

Expiry date

01/01/0001

Mai Takanashi

Author

Mai Takanashi
Read more Shortlist Save this role
Feasibility Analytics Manager (Advanced)

Salary

Location

US, Blue Bell (PRA)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Study Start Up

Job Type

Permanent

Description

What you will be doing: Delivery of clinical trial analytics and insight generation with regards to feasibility operations and predictive trial enrollment. The FAM will interact directly with various

Reference

JR137766

Expiry date

01/01/0001

Monica Hawkins Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above