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Trial Graphics Jobs in Oregon (NOW HIRING)

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Trial Graphics information

See Oregon salary details

$52.9K

$127.7K

$203.5K

How much do trial graphics jobs pay per year?

As of Aug 2, 2026, the average yearly pay for trial graphics in Oregon is $127,736.00, according to ZipRecruiter salary data. Most workers in this role earn between $99,400.00 and $146,400.00 per year, depending on experience, location, and employer.

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

To thrive in a Trial Graphics role, you need expertise in visual communication, graphic design, and an understanding of legal processes, often supported by a degree in graphic design, visual arts, or a related field. Familiarity with design software like Adobe Creative Suite, 3D modeling tools, and presentation platforms such as PowerPoint is critical, and prior experience with trial presentation software is highly valued. Strong attention to detail, collaboration, time management, and the ability to translate complex information into compelling visuals set top candidates apart. These skills ensure that intricate legal arguments are clearly communicated to judges and juries, supporting successful trial outcomes.

What are the typical daily tasks and responsibilities for someone working in Trial Graphics?

Professionals in Trial Graphics spend their days creating visual aids such as timelines, charts, animations, and diagrams to help legal teams clearly present complex information in court. This often involves working closely with attorneys, paralegals, and expert witnesses to understand case details and visualize critical evidence. Responsibilities also include revising graphics based on feedback, managing tight deadlines, and ensuring all materials adhere to legal standards. You may also be responsible for operating presentation equipment in the courtroom or during mediation, making teamwork and adaptability essential to the role.

What is a Trial Graphics job?

A Trial Graphics job involves creating visual presentations to help attorneys communicate complex information during trials, hearings, and arbitrations. This includes designing demonstrative exhibits, timelines, charts, medical illustrations, and animations to clarify key points for judges and juries. Professionals in this field use graphic design, animation, and legal knowledge to develop persuasive visuals that support legal arguments. They work closely with attorneys, expert witnesses, and litigation teams to ensure accuracy and effectiveness.

What are popular job titles related to Trial Graphics jobs in Oregon? For Trial Graphics jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Trial Graphics jobs in Oregon look for? The top searched job categories for Trial Graphics jobs in Oregon are:
Trial Graphics jobs near you
Infographic showing various Trial Graphics job openings in Oregon as of July 2026, with employment types broken down into 1% Internship, 84% Full Time, 12% Part Time, 1% Temporary, and 2% Contract. Highlights an 82% Physical, 4% Hybrid, and 14% Remote job distribution, with an average salary of $127,736 per year, or $61.4 per hour.

Associate Director, Medical Writing (Clinical and Regulatory)

Ultragenyx Pharmaceutical

OR • Remote

Other

Posted 11 days ago

Job description

Position Summary:

ultrafocused - Work together to fearlessly uncover new possibilities

The Associate Director, Medical Writing will be responsible for writing and coordinating the writing of various clinical and regulatory documents, including protocols/amendments, investigator brochures, clinical study reports, and NDA/BLA submission documents. The Associate Director, Medical Writing will work closely with cross-functional teams to manage the preparation of written clinical and regulatory documents, ensuring that they are of high quality and completed in a timely fashion compliant with SOPs, ICH/GCP/regulatory guidelines, and company goals. The Associate Director will be seen as a key SME for medical writing, providing leadership across global teams.

Work Model: 

Remote: Officially documented as working full-time from home, with travel to Ultragenyx's offices or other locations on occasion as needed.

Responsibilities:

1. Development and implementation of cross-functional input for clinical and regulatory documents including the drafting, editing, reviewing, and ensuring quality of key messages, protocols, investigator brochures, clinical study reports, INDs, eCTD/NDA clinical summaries, response documents, and briefing books

2. Ensures smooth, effective, and timely document management from start (template) to finish (approval), which may include: first-draft authoring, literature and reference retrieval, editing, efficient comment resolution, and managing various processes (e.g., reviews, QC, QA, formatting, publishing, document archiving) with high quality

3. Actively supports cross-functional project teams as the Clinical Regulatory Writing representative, providing input to ensure timely and accurate deliverables and negotiating timelines as necessary

4. Proactively implements clinical transparency and disclosure practices in document development (e.g. Policy 70, Clintrials.gov, etc.) and partners with Clinical Trial and Transparency colleges.

5. Develops effective collaborative relationships with other key functional stakeholders

6. Participates in department initiatives with other Clinical Regulatory Writing members to formulate writing strategies and standards to be implemented and takes responsibility for execution.

7. Distills large amounts of clinical and scientific data into essential elements for tabular and graphical display

8. Ensures that all documents are written in compliance with relevant clinical and regulatory requirements including continual knowledge of ICH and Health Authority guidance.

Requirements:

1. BS, MS, or doctorate in a scientific or medical field

2. Six+ years in the biotechnology/pharmaceutical industry

3. Demonstrated experience in medical writing, editing, and clinical development; has written protocols, IBs, CSRs; worked on at least one eCTD/NDA submission a plus.

4. Strong leadership, planning, and project management skills, along with initiative and ability to be productive with minimal supervision and minimal administrative support

5. Demonstrated ability to work effectively in a fast-paced environment with multiple high priority projects

6. Proven ability to develop and implement medical writing processes and standards

7. Exceptional oral and written communication skills

8. Understands and effectively responds to multicultural communication styles and business practices with alliance partners and internal colleagues

9. Flexible; adapts work style to meet organization needs

10. Strong organizational abilities and experience in a multitasking environment

11. Motivated, self-directed, and able to work autonomously and in team settings to meet aggressive organizational goals

12. Dedication to quality and reliability

13. Excellent computer skills (Microsoft Office Suite, Power Point, Adobe Illustrator, figures and graphic design; Project and Visio a plus)

14. Ability to build and maintain effective partnerships, both internally and externally

15. Holds self and others accountable for adherence to high ethical standards; adopts and maintains the utmost integrity and respect for colleagues at all levels

16. Rare disease experience and/or gene therapy experience a plus

17. Ability and willingness to travel several times a year

#LI-CS1 #LI-Remote

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