TMF Lead

ICON Clinical Research; A distancia; MXN 200,000 - 400,000; Jornada completa

Descripción de la vacante

A leading clinical research organization is seeking a Trial Master File Lead to oversee TMF management processes in Mexico. The role requires a Bachelor's degree and strong experience in TMF and regulatory compliance. You will lead TMF quality checks, collaborate with teams, and provide training on best practices. The company offers competitive salaries and benefits, emphasizing well-being and work-life balance. Fluent English is a must for this home-based position.

Servicios

Various annual leave entitlements

Health insurance

Retirement planning offerings

Employee Assistance Programme

Flexible optional benefits

Formación

• Proven experience in TMF management within the healthcare industry.
• Strong understanding of regulatory requirements for clinical documentation.
• Excellent organizational skills to ensure compliance and accuracy.

Responsabilidades

• Lead TMF setup, maintenance, and oversight.
• Collaborate with teams for timely TMF documentation.
• Conduct quality checks and audits on the TMF.

Conocimientos

TMF management

Regulatory compliance

Document management

Collaboration

Attention to detail

Communication skills

Fluency in English

Educación

Bachelor's degree in life sciences, nursing, or business administration

Advanced degree preferred

Descripción del empleo

Trial Master File Lead - Mexico (Homebased)

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.

Role

Trial Master File Lead

Location

Mexico (Homebased)

We are currently seeking a Trial Master File Lead to join our diverse and dynamic team. As a TMF Lead at ICON, you will be responsible for overseeing the Trial Master File (TMF) management processes, ensuring compliance with regulatory requirements and best practices in clinical trials. Your expertise will be essential in maintaining the integrity of the TMF and supporting efficient document management throughout the trial lifecycle.

What You Will Be Doing

• Leading the setup, maintenance, and oversight of the TMF in compliance with regulatory standards and internal policies.
• Collaborating with cross‑functional teams to ensure timely and accurate documentation within the TMF.
• Conducting regular TMF quality checks and audits to identify and resolve discrepancies or issues.
• Providing training and support to team members on TMF processes and best practices.
• Establishing and implementing strategies for continuous improvement in TMF management and documentation practices.

Your Profile

• Bachelor's degree in a relevant field such as life sciences, nursing, or business administration; advanced degree preferred.
• Proven experience in TMF management or clinical trial document management, preferably within the healthcare or clinical research industry.
• Strong understanding of regulatory requirements and industry standards related to TMF and clinical documentation.
• Excellent organizational skills and attention to detail, ensuring compliance and accuracy in TMF management.
• Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams.
• Fluency in English

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.