CRA I

ICON Strategic Solutions; México; Presencial; MXN 549,000 - 825,000; Jornada completa

Descripción de la vacante

A global leader in clinical research is seeking a Clinical Research Associate (CRA) to coordinate clinical monitoring and site management. You will ensure compliance with regulations and support studies through effective communication and problem-solving. Candidates should have a Master's degree in biomedical sciences or a related field, and at least 1 year of experience in clinical research monitoring. The role offers competitive salary and comprehensive benefits.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible optional benefits

Formación

• First working experience in clinical research monitoring (at least 1 year of experience).
• Communicative skills in English.
• Heart for clinical research and for your assigned studies/sites.

Responsabilidades

• Identify, select, initiate and close-out study sites for clinical trials.
• Monitor studies to ensure protocol compliance.
• Reply and resolve queries from monitoring visits.
• Report safety issues and write monitoring reports.
• Plan the next visits.

Conocimientos

Clinical research monitoring

Communication skills in English

Problem-solving

Educación

Master degree in biomedical sciences or bachelor in a paramedical field

Descripción del empleo

Overview

As a CRA you will coordinate all aspects of the clinical monitoring and site management process in accordance with regulatory guidelines, local regulations and standard operating procedures. In this role you will be a decision maker, solving problems independently but always as part of the client and ICON plc team.

What you will be doing

• Identify, select, initiate and close-out of the study sites for clinical trials
• Study monitoring to ensure protocol compliance
• Reply and resolve queries that are being identified during the monitoring visits
• Reporting of safety issues
• Writing of monitoring reports and planning the next visits

You are

By preference you hold a Master degree in biomedical sciences or a bachelor in a paramedical field.

• First working experience in clinical research monitoring (at least 1 year of experience). Of course, we also welcome more experienced candidates and adapt the role in function of your experience.
• Communicative skills in English
• Heart for clinical research and for your assigned studies/sites
• You love to communicate with different stakeholder and love to encourage people, drive them and being the point of contact for your studies

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, 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, 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.

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.