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Clinical Trial Associate

ICON Clinical Research

Ciudad de México

Presencial

MXN 400,000 - 600,000

Jornada completa

Ayer
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Descripción de la vacante

A leading clinical research organization based in Mexico City seeks candidates for a role focused on data management and support for clinical trials. The successful applicant will perform tasks such as data entry, document management, and vendor support, requiring attention to detail and strong organizational skills. Candidates should have an Associate’s degree and ideally 3 years of experience in life sciences. The position offers competitive salary and benefits designed for work-life balance.

Servicios

Various annual leave entitlements
Health insurance offerings
Competitive retirement planning
Global Employee Assistance Programme
Flexible optional benefits

Formación

  • 3 years work experience in life sciences or medically related field is preferred.
  • Proficient in the use of various computer software.

Responsabilidades

  • Data entry and data management of CTMS.
  • ICF tracking and reconciliation.
  • Support vendor management and meeting coordination.
  • Assist in investigator meeting planning and documentation.

Conocimientos

Attention to detail
Good verbal communication skills
Good written communication skills
Organizational skills
Ability to multi-task

Educación

Associate’s degree or higher education

Herramientas

MS WORD
Excel
Power Point
Descripción del empleo
Overview

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. This role is Mexico-based and office-based.

Responsibilities
  • Data entry and data management of CTMS
  • ICF tracking and reconciliation
  • Document management including essential document filing and TMF reconciliation
  • Support vendor management: compile meeting agendas, minutes; reconcile vendor reports; assist with coordinating delivery of materials for SIV
  • Investigator meeting support, assist in meeting planning, drafting and finalizing agenda, attendee expense reports
  • Coordinate site equipment provisioning
  • Coordinate investigator brochure translation, printing and distribution
Knowledge
  • Proficient in the use of computer and software such as MS WORD, Excel, Power Point, etc.
  • Good verbal and written communication skills (English and regional)
  • Attention to detail and ability to multi-task
  • Good organizational, record retention and time management skills
Key competencies
  • Attention to detail
  • Delivery focus
  • Team work
  • Time management
  • Policy, process and procedural conformance
Basic qualifications
  • Associate’s degree or higher education
Preferred qualifications
  • 3 years work experience in life sciences, or medically related field
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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

Visit our careers site (https://careers.iconplc.com/benefits) 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 (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.

Are you a current ICON Employee? Please click here (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply

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