Lead Analytical Monitor

ICON Strategic Solutions; México; Presencial; MXN 400,000 - 600,000; Jornada completa

Descripción de la vacante

A leading healthcare intelligence organization in Mexico is seeking a Central Review Lead to oversee clinical trials and coordinate centralized review activities. The ideal candidate will have a strong background in clinical research, excellent leadership skills, and experience in managing complex projects. This role offers a competitive salary and a range of benefits, including health insurance and retirement planning options, aimed at enhancing work-life balance.

Servicios

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Flexible country-specific optional benefits

Formación

• Extensive experience in clinical research, data management, or study coordination in the CRO industry.
• Strong understanding of central review methodologies and regulatory requirements.
• Ability to collaborate effectively with stakeholders at all levels.

Responsabilidades

• Lead and oversee the planning and execution of centralized review activities.
• Collaborate with study teams and clinical sites to ensure accurate data collection.
• Implement processes and quality control measures for centralized review operations.
• Provide leadership to central review teams, ensuring adherence to protocols.
• Identify and address issues related to central review activities.

Conocimientos

Leadership

Project management

Communication

Problem-solving

Educación

Bachelor's or advanced degree in Life Sciences or related field

Descripción del empleo

Lead Analytical Monitor. 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 Central Review Lead to join our diverse and dynamic team. As a Central Review Lead at ICON, you will play a pivotal role in overseeing and coordinating centralized review activities for clinical trials, contributing to the advancement of inNvative treatments and therapies.

What you will be doing

• Lead and oversee the planning, execution, and monitoring of centralized review activities, including imaging assessments, laboratory analyses, and other centralized evaluations.
• Collaborate closely with study teams, clinical sites, and external vendors to ensure the timely and accurate collection, transfer, and interpretation of clinical trial data.
• Develop and implement standardized processes, protocols, and quality control measures to optimize the efficiency, accuracy, and reliability of centralized review operations.
• Provide leadership and guidance to central review teams, ensuring adherence to protocol requirements, regulatory standards, and best practices.
• Proactively identify and address issues, deviations, and risks related to central review activities, driving continuous improvement and operational excellence.

Your profile

• Bachelor's or advanced degree in Life Sciences, Health Sciences, or a related field.
• Extensive experience in clinical research, data management, or study coordination within the pharmaceutical, biotechNlogy, or CRO industry.
• Strong leadership and project management skills with a track record of successfully leading cross‑functional teams and managing complex projects.
• In-depth kNwledge of central review methodologies, techNlogies, and regulatory requirements (e.g., ICH GCP, FDA regulations).
• Excellent communication, interpersonal, and problem‑solving abilities, with the ability to effectively collaborate and communicate with stakeholders at all levels.

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.

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 to apply.