Avania logo

Project Coordinator

Avania

Remote · USJobup to $70K/yrSeen 1w agoSeen in employer's feed 2 days ago

Most applications go out cold — see where you stand first. No sign-up to start.

Watch jobs like this.

At a glance

Compensation
up to $70K/yr
Location
Remote · US
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

Avania is hiring a Project Coordinator specializing in eTMF and CTMS for a US-based remote role. The position focuses on independent Trial Master File quality control, identifying and resolving documentation issues, and supporting trial documentation across client projects and Avania-managed studies. It also includes TMF filing and transfers, progress reporting, project coordination tasks, and improving internal quality control processes. Around 3–5 years of relevant experience is sought.

Skills & qualifications

RequiredNice to have

Skills

eTMF WorkCTMS WorkTMF FilingTMF Quality ControlDocumentation Query ResolutionClear CommunicationMicrosoft ToolsSharePointVeeva VaultMedidata RaveSiteroSmartsheet

Qualifications

3+ Years Relevant Experience

Full job description

Avania are hiring - Project Coordinator - eTMF/CTMS Specialist

Salary up to $70,000 + Annual Bonus + Benefits

About the Role

Join Avania in a US-based remote role focused on electronic Trial Master File (eTMF) quality control and Clinical Trial Management System (CTMS) support. You'll help improve the quality of trial documentation across client projects and Avania-managed studies, working with project managers and project coordinators to identify and resolve documentation issues.

The role combines specialist eTMF/CTMS work with some project coordination responsibilities. Its primary focus is independent TMF quality control, separating document review from the work of uploading and filing documents.

What You'll Do

  • Perform TMF quality control reviews, identify documentation issues, and issue, respond to, and follow up on queries through resolution.

  • Support TMF filing, cleanup, and transfers, with final transfer sign-off retained by the senior specialist.

  • Work in eTMF and CTMS platforms to support trial documentation and study teams.

  • Report concise progress metrics, including time spent and documents or folders reviewed.

  • Support project coordination as needed, including assigning training, preparing meeting agendas and minutes, and maintaining accompanying meeting logs.

  • Help improve internal TMF quality control processes alongside project managers, project coordinators, and the senior specialist.

Candidates who offer a combination of the skills, knowledge and experience listed below are encouraged to apply. With our continued growth we are hiring talent to join us on our journey and grow with us.

What You'll Bring

  • Hands-on experience in eTMF/CTMS work, including TMF filing, quality control, and resolving documentation queries. We're looking for someone with around 3-5 years of relevant experience who is comfortable working in these systems.

  • The ability to follow a documentation quality issue through to resolution and communicate progress clearly.

  • Proficiency with Microsoft tools, including SharePoint.

Experience with Veeva Vault is particularly valuable. Familiarity with Medidata Rave, Sitero and other eTMF/CTMS platforms would also be helpful. Smartsheet experience is a plus, not a requirement.

Avania - MedTech's trusted Champion

We look forward to receiving your application!

Avania takes pride in being an equal opportunity employer. We consider qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

#LI-DNI

Similar jobs, posted recently

Open roles like this one, listed in the last 30 days.

You've read the whole posting — now see how you match it.