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.
A commitment to promoting equity and inclusion in all aspects of TMF management.
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Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .
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Benefits
Health insuranceDental insuranceVision insuranceRemote work optionsEquity / stock options
Additional Information
TMF Lead - Remote - Mexico
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
We are currently seeking a TMF 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.
Icon · Mexico City, Mexico