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Tmf Jobs in Oregon (NOW HIRING)

Natera

OR · On-site

Familiarity with the organization and structure of the Trial Master File (TMF) * Familiarity with bio sample management, sample processing, and biobanking best practices * Competency in SOPs, ICH-GCP ...

Syneoshealth

OR · On-site

Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local ...

Syneoshealth

OR · On-site

Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local ...

Syneos Health/ inVentiv Health Commercial LLC

OR · On-site

Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to ...

Syneoshealth

OR

Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to ...

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Tmf information

See Oregon salary details

$18

$42

$74

How much do tmf jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for tmf in Oregon is $42.28, according to ZipRecruiter salary data. Most workers in this role earn between $34.04 and $46.49 per hour, depending on experience, location, and employer.

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

To thrive as a TMF (Trial Master File) Specialist, you need a solid understanding of clinical trial documentation, regulatory guidelines (such as ICH-GCP), and strong organizational skills, typically supported by experience in clinical research or a related life sciences field. Proficiency with electronic Trial Master File (eTMF) systems, document management software, and sometimes certifications like DIA TMF or clinical research certification are commonly required. Attention to detail, effective communication, and the ability to manage deadlines are important soft skills in this role. These competencies ensure regulatory compliance, efficient document retrieval, and successful clinical trial audits.

What is a TMF?

A TMF (Trial Master File) job typically involves managing and maintaining essential documents related to clinical trials. Professionals in this role ensure that all trial documentation complies with regulatory requirements and is audit-ready. They may work with electronic TMF (eTMF) systems, collaborate with study teams, and ensure document accuracy and completeness. TMF specialists play a crucial role in supporting clinical research compliance and regulatory submissions.

What are the main responsibilities of a TMF specialist on a daily basis?

As a TMF Specialist, your daily responsibilities include maintaining and updating essential clinical trial documents, ensuring accurate filing and compliance with regulatory standards, and performing routine quality checks on documentation. You will collaborate closely with clinical operations, project managers, and external stakeholders to gather and validate needed materials. Attention to deadlines and meticulous organization are critical, as audits and inspections may require quick access to correctly archived files. This hands-on role is vital for ensuring that all documentation is complete, accurate, and ready for review throughout the life cycle of a clinical trial.

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Tmf jobs near you
Infographic showing various Tmf job openings in Oregon as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $87,934 per year, or $42.3 per hour.

Senior Clinical Trial Manager (CTM)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Other

Re-posted 4 hours ago

Job description

Senior Clinical Trial Manager (CTM) 

Location:   This position may be performed remotely with travel to the Boston area as needed.   

Position Summary 

This role will be responsible for project management in the initiation, execution and close out of domestic and international clinical studies, including study concept and design, feasibility assessments, study start-up, contract and budget oversight, data exchange and support of data analysis and interpretation. 

This position requires both the knowledge and experience to work within established clinical trial paradigms while exploring and embracing new approaches to conducting research to support data aggregation and analysis to advance patient care. The Sr. CTM will participate on clinical project teams to achieve quality results in a cost-effective and timely manner. S/he will be a key team member to establish key practices and procedures for the clinical team. 

Primary Responsibilities 

  • Manage study activities in the successful execution of clinical trials from protocol concept to clinical study report, complying with Good Clinical Practice (GCP) guidelines and international regulations 
  • Manage strategic engagement with key collaborators 
  • Set-up and oversee clinical trial-related trackers such as regulatory documents, trial master file (TMF), startup progress, screening/enrollment, study invoices/payments, project budgets, etc. 
  • Key contributor to IRB/EC and regulatory submissions 
  • Oversee TMF reviews to ensure completeness and inspection readiness 
  • Regularly review documents to ensure adherence to Clinical Operations and/or project specific quality requirements (e.g. SOPs, work practices, training guides) 
  • Identify and mitigate against study risks, escalating as necessary 
  • Direct initiatives to identify and implement best practices and continuous improvement plans in clinical development 

Education and Professional Experience 

  • Bachelor's degree in a scientific field required; advanced scientific degree a plus 
  • 5+ years directly managing clinical trials in Sponsor or CRO setting 
  • In-depth knowledge of clinical trial operations, ICH, GCP Guidelines and other applicable regulatory requirements 
  • Experience directing members of clinical operations teams 
  • Experience working in a team across multiple functional areas (e.g., Quality Assurance, Data Management, Biostats, Medical Writing, Safety, Clinical Supply, Finance) 

Other Essentials and Key Success Factors 

  • Intellectual curiosity, innovation and creative problem solving with an entrepreneurial spirit 
  • Ability to think critically in fast-paced projects with a keen sense of urgency and demonstrated ability to problem solve 
  • Self-motivated and able to work autonomously, as well as a member of a collaborative team 
  • Highly-organized and detail-oriented with a passion to deliver quality results 
  • Strong verbal and written communication skills with an ability to build relationships internally and externally 
  • Highest levels of professionalism, confidence, personal values and ethical standards 

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