Clinical Research Coordinator - Part time - Fixed term

ICON; Ciudad de México; A distancia; MXN 200,000 - 400,000; A tiempo parcial

Descripción de la vacante

A world-leading healthcare organization seeks a part-time Clinical Research Coordinator to work from home in Mexico. In this role, you'll coordinate clinical studies, support researchers, and ensure compliance with medical regulations. A Bachelor's degree in a related field and experience in clinical research are required. This opportunity offers competitive compensation and a range of benefits designed to prioritize your well-being and work-life balance.

Servicios

Various annual leave entitlements

A range of health insurance offerings

Competitive retirement planning offerings

Global Employee Assistance Programme

Life assurance

Flexible country-specific optional benefits

Formación

• 6+ months experience working in clinical research or healthcare settings.
• Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Availability to work part time (24 hours a week) in a fixed term contract.

Responsabilidades

• Facilitating the coordination and execution of clinical research studies.
• Collaborating with principal investigators, study sponsors, and regulatory authorities.
• Collecting and maintaining accurate and complete clinical trial data.
• Managing study-related documentation.
• Providing support and guidance to study participants.

Conocimientos

Organizational skills

Communication skills

Interpersonal skills

Detail-oriented

Educación

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Descripción del empleo

Clinical Research Coordinator - Homebased - Mexico

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.

We are currently seeking a part time Clinical Research Coordinator to join our diverse and dynamic team. As a Clinical Research Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

• Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities.
• Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards.
• Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes.
• Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions.
• Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures.

Your profile

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• 6+ months experience working in clinical research or healthcare settings.
• Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements.
• Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment.
• Detail-oriented with the ability to manage multiple tasks and priorities simultaneously.
• Availability to work part time (24 hours a week) in a fixed term contract.

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 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