TMF Quality Review Jr. Associate
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 1d ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 2d ago
The date the source published, not the day we noticed it (2026-10-09). Last seen at its source 1h ago.
We have tracked this listing since 10 Oct 2026 (1 days). The employer's own board has carried it every time we have read it, most recently 1 hour ago.
Is it remote?
The listing says yes
The location field doesn't say remote, so our assessment is based on the title or the description. Read the listing before applying.
Who may apply?
Mexico
The description states no restriction of its own. This is the source's own tag.
Skills named in the ad
Recognised terms only, from a fixed vocabulary — this is what CV matching compares against.
Carried by 1 source
-
Workday employer's own board first seen 1d ago · last seen 1h ago
The listing
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Trial Master File (TMF) Specialist III at ICON, you will participate in client services contracts and internal business needs by managing Trial Master File (TMF) documentation.
What You Will Do:
You will take responsibility for trial master file management deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
- Manage Trial Master File (TMF) documentation in accordance with client requirements and ICON procedures
- Ensure the completeness, accuracy, and timeliness of TMF documentation throughout the lifecycle of clinical trials
- Partnership with cross-functional teams to collect, review, and maintain essential documents for regulatory submissions
- Conduct quality checks and audits of TMF documents to ensure compliance with regulatory standards and sponsor requirements
- Provide efforts and guidance to internal and external stakeholders on TMF-related matters
Your Profile:
You will bring relevant trial master file management experience, along with the following qualifications and skills.
Required qualifications and experience:
- A minimum of 3 years of experience in clinical research or document management within the pharmaceutical, biotechnology, or CRO industry
- Bachelor's degree in life sciences, documentation management, or a related discipline
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks simultaneously
- Excellent communication skills, with the ability to partnership effectively with cross-functional teams
- Bachelor's degree in a relevant field preferred
- Willingness to travel as required (approximately 5%)
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.
Are you a current ICON Employee? Please click here to apply