For Employers

ICON plc

TMF Quality Review Jr. Associate

Posted 2 days ago
2-5 years experience
Apply Now

Please mention DailyRemote when applying

?
Resume Match Score

See how much of this job your resume covers, and what’s missing.

Want a recruiter to go through it line by line?

Get professional review

Create a cover letter for this job

Upload your resume and we draft a letter for this exact role, tailored to what it asks for.

  • Tailored to this role
  • Based on your resume
  • Fully editable
AI Summary

Manage Trial Master File (TMF) documentation to ensure completeness, accuracy, and timeliness throughout the clinical trial lifecycle. Partner with cross-functional teams to conduct quality checks and maintain essential documents for regulatory compliance.

Home Based - Mexico - TMF

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

Automatically Apply to the Best Remote Jobs

Stop the endless job search. Our AI finds and applies to the best jobs for you.

Try it Now
Keep looking

Similar Jobs

See all Remote Others jobs →

Casual Study Grant Application Form 2027 - Casual Bay Venues Staff Only

Contract New Zealand Others

Plumbing license qualifier

Full Time United States $50000 - $70000 per year Others

UoW 20% Discount Registration Form 2027 - Bay Venues Permanent Staff Only.

Contract New Zealand Others

Research Associate

Full Time United States $16 per hour Others

Work When You Want Paid Research Studies - Greeley, CO

Part Time United States Others

Reputation Management Coordinator

Full Time United States $20 - $23 per hour Others
Apply Now

Personalize your Remote Job Search in 3 Easy Steps!

Featuring 215,118+ Jobs in Others

Answer easy questions

Answer easy questions

215,118+ jobs across 15+ categories

Get your best job matches

Get your best job matches

Only hand-screened, legit jobs

Find a remote job faster

Find a remote job faster

No ads, scams, or junk

“I was the first applicant for a remote marketing position that got listed on the company website the same day I applied. Had an interview within 48 hours!”

Sarah J. — Sarah J. · Marketing Manager ★★★★★ Verified