ZipRecruiter

Log In

1

Tmf Support Analyst Jobs (NOW HIRING)

Daiichi Sankyo, Inc.

... TMF) requirements.For outsourced studies, oversee statistical programming vendor on project ... Provide programming support to prepare regulatory requested analyses and help submission team in ...

Alira Health

Supervises and provides support to the Clinical team, including Clinical Assistants, In-house ... Assists in TMF management and manages TMF reviews as needed. * Prepares for and participates in ...

Noblesoft Technologies

Tandem Developer

Chicago, IL · On-site

Analysis and Design * Analyze business requirements and translate them into technical ... Collaboration and Support * Provide technical support and guidance to other team members and end ...

next page

Showing results 1-20

All JobsTmf Support Analyst Jobs

Tmf Support Analyst information

See salary details

$18

$39

$62

How much do tmf support analyst jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for tmf support analyst in the United States is $39.80, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $45.67 per hour, depending on experience, location, and employer.

What is a TMF Support Analyst?

A TMF Support Analyst is a professional who manages and maintains the Trial Master File (TMF) in clinical research settings. Their main responsibilities include ensuring the completeness, accuracy, and regulatory compliance of clinical trial documentation. TMF Support Analysts work closely with clinical teams to organize, review, and audit essential documents, helping to ensure smooth clinical trial operations and successful regulatory submissions. They also troubleshoot TMF-related issues and provide guidance on best practices for document management.

What are the key skills and qualifications needed to thrive as a TMF Support Analyst, and why are they important?

To thrive as a TMF Support Analyst, you need a solid understanding of Trial Master File (TMF) processes, clinical documentation standards, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with electronic TMF (eTMF) systems, document management tools, and knowledge of ICH-GCP guidelines are typically required. Attention to detail, strong organizational skills, and effective communication are vital soft skills in this role. These competencies ensure accurate document management, regulatory readiness, and smooth collaboration within clinical research teams.

What is the difference between Tmf Support Analyst vs Tmf Business Analyst?

AspectTmf Support AnalystTmf Business Analyst
Primary RoleProvides technical support and troubleshooting for Tmf systemsAnalyzes business needs and recommends system improvements
Required SkillsTechnical knowledge of Tmf platforms, problem-solvingBusiness process understanding, communication skills
CertificationsIT support or Tmf-specific certifications often preferredBusiness analysis certifications like CBAP may be advantageous
Work EnvironmentIT support teams, technical departmentsBusiness units, project teams

The Tmf Support Analyst primarily focuses on technical support and issue resolution within Tmf systems, while the Tmf Business Analyst concentrates on understanding business needs and implementing system solutions. Both roles require familiarity with Tmf platforms but serve different functions in the organization.

How does a TMF Support Analyst typically collaborate with clinical trial teams to ensure timely document management?

A TMF Support Analyst works closely with clinical trial teams, including clinical operations, regulatory affairs, and quality assurance, to ensure that essential trial documents are accurately uploaded, tracked, and maintained within the Trial Master File (TMF) system. They facilitate regular communication with study teams to clarify documentation requirements, resolve discrepancies, and support audit readiness. This collaborative approach helps maintain compliance with regulatory standards and ensures that all documentation is up-to-date throughout the study lifecycle.
What cities are hiring for Tmf Support Analyst jobs? Cities with the most Tmf Support Analyst job openings:
What states have the most Tmf Support Analyst jobs? States with the most job openings for Tmf Support Analyst jobs include:

Data Acquisition Specialist

RIT Solutions Inc/ Tech Dev IT/ Texperts Inc/ConceptsIT, Inc.

Glendale, CA • On-site

Other

Posted 29 days ago

Job description

Serve as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level and manage study start up, conduct and close out activities.
Create external data transfer agreements, ensuring external clinical trial data are in alignment with company Standards and specifications to support data integration, analysis, and reporting.
Help and advice in setting up infrastructure for external data, to flow into company Clinical data pipelines.
Responsible for validation of all 3rd Party Data generated in clinical trial into company Clinical Data pipelines.
Develop strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members.
Participate in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit.
Representing company in interactions with key external partners as part of company CT3 3rd Party Data Acquisition team.
Responsible for timely submission and on-going maintenance of study related 3rd Party Data Acquisition documentation in TMF.
Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes.
Liaise with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) performing services on behalf of company.
Escalate issues to CT3 leadership appropriately.
Technical/Functional Expertise
Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles.
Experience with all phases of drug development.
Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors.
May lead study level negotiation and agreement for data transfer or integration on behalf of company.
Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required.
Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus.

Apply