Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

ProPharma

TMF Specialist (FSP)

Career Insights for Archivist

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Massachusetts data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

An Archivist manages and organizes storage of records and historic information or collections. Reviews and appraises material, determines items to archive and conditions necessary to preserve materials safely. Develops systems for documenting and organizing material to be archived. May use archival material for research or assist other researchers with access to an archive.

$73,420 / year median in Massachusetts

+7% projected growth

Explore Career

Job Description

TMF Specialist (FSP) at ProPharma TMF Specialist (FSP) at ProPharma in Burlington, Massachusetts Posted in 1 day ago.

Type:

full-time

Essential Functions:

Support Trial Master File (TMF) set-up, maintenance, update, archival and closeout (if applicable) in accordance with company SOPs, sponsor requirements, and applicable regulations. Reviews, edits, formats master documents according to approved procedures and templates, maintains document properties (metadata), monitors document status and approval notifications, distributions, and archiving. Conduct detailed and appropriate quality checks (QC) on TMF documents at defined time points, including any paper originals required. Ensure that privacy and security standards are met and adhered to. Ensure that documents are maintained in accordance with retention practices. Assist in routine internal and external master file audits to ensure compliance with applicable work instructions, Standard Operating Procedures (SOPs), Regulatory requirements, ICH and GCP guidelines. Other duties as assigned.

Necessary Skills and Abilities:

Effective communication, and interpersonal skills with ability to partner with cross functional internal and external stakeholders. Must be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures. Exhibits a good understanding of general quality assurance concepts and practices. Highly organized with a strong attention to detail. Proficiency in web-based systems and project management applications (e.g., Microsoft Office, Point, etc.). Experience with Veeva Clinical