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Remote Etmf Jobs in California (NOW HIRING)

Remote based in United States. What You'll Do * Coordinate and support delivery of Phase I clinical ... Manage systems such as CTMS and eTMF, ensuring accuracy and compliance. * Act as a key point of ...

Remote based in United States. What You'll Do * Coordinate and support delivery of Phase I clinical ... Manage systems such as CTMS and eTMF, ensuring accuracy and compliance. * Act as a key point of ...

Senior Manager, Clinical Compliance

Irvine, CA · On-site +1

$160K - $170K/yr

Remote - Home Office Summary: Reporting to the Vice President, Clinical Affairs, the Senior Manager ... and eTMF/document management systems. Physical Requirements: * Standard office environment ...

Remote Etmf information

What is a remote eTMF?

A Remote eTMF (electronic Trial Master File) job involves managing and maintaining digital clinical trial documentation from a remote location. Professionals in this role ensure regulatory compliance, organize essential trial records, and facilitate audits. They work with sponsors, CROs, and regulatory bodies to ensure proper documentation throughout a clinical study. Strong knowledge of GCP (Good Clinical Practice) guidelines and document management systems is typically required. This role is essential in supporting the smooth execution of clinical trials while ensuring regulatory requirements are met.

What are the main daily responsibilities of a remote eTMF?

As a Remote eTMF Specialist, your daily responsibilities typically include uploading, reviewing, and maintaining essential clinical trial documents within electronic Trial Master File systems to ensure proper organization and compliance. You will regularly collaborate with clinical project teams, regulatory personnel, and external partners to track document statuses and resolve any discrepancies. Ensuring all documentation meets internal quality standards and regulatory requirements is a key focus. This role also often involves preparing the eTMF for audit and inspection readiness, which requires strong attention to detail and proactive communication.

What are the key skills and qualifications needed to thrive in the remote eTMF position, and why are they important?

To thrive as a Remote eTMF (electronic Trial Master File) Specialist, you need strong knowledge of clinical trial documentation, GCP (Good Clinical Practice) compliance, and previous experience working in clinical research or regulatory affairs. Proficiency with eTMF systems such as Veeva Vault, Medidata, or MasterControl, along with familiarity with regulatory guidelines, is typically required. Excellent attention to detail, organizational skills, and effective remote communication abilities set top candidates apart. These skills ensure that clinical trial documentation is accurate, audit-ready, and compliant with regulations in a virtual work environment.

What are the most commonly searched types of Etmf jobs in California? The most popular types of Etmf jobs in California are:
What cities in California are hiring for Remote Etmf jobs? Cities in California with the most Remote Etmf job openings:
Infographic showing various Remote Etmf job openings in California as of August 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 100% Remote job distribution.

Veeva Project Lead

Lorven Technologies

Foster City, CA • On-site, Remote

Full-time

Re-posted 4 days ago


Job description

I hope you are doing well,
Please share your updated profile if you are interested in the below role.
Our client seeks an Veeva Project Lead Data Migration for a Full Time project in Remote .Below is the detailed requirement
Job Title: Project Lead Veeva Data Migration
Work location : Remote
Duration: Full Time
Job Description:
  • Bachelor's degree preferably in Computer Science, Information technology, Computer Engineering, or related IT discipline or equivalent experience with 12+ Minimum Experience
  • 4+ years managing Veeva CTMS and eTMF systems for configuration, user support, and compliance management.
  • 4+ years ensuring data integrity and migration with focus on validation, cleanup, and accurate transfer across GxP-regulated systems.
  • 4+ years leading project execution and management including planning, tracking deliverables, and resolving system/data-related issues.
  • 4+ years supporting system validation and documentation aligned with 21 CFR Part 11 and CSA guidelines.
  • 4+ years collaborating with cross-functional teams to improve system performance, ensure audit readiness, and maintain compliance.

Lorven technologies logo

About Lorven technologies

Sourced by ZipRecruiter

Lorven Technologies, headquartered in Plainsboro, New Jersey, United States, is a reputable company in the technology industry, specializing in providing effective IT solutions and consulting services. The company's official website, lorventech.com, offers comprehensive insights into its offerings which include but are not limited to software development, IT consulting, project management, and business analysis. Since its inception, Lorven Technologies has been committed to ensuring efficiency and reliability in delivering IT services to its global clientele, establishing itself as a trusted name in the industry.

Industry

It services

Company size

51 - 200 Employees

Headquarters location

Plainsboro, NJ, US

Year founded

2001

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