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Contract Medical Writing Jobs in Oregon (NOW HIRING)

Capitol Bridge, LLC.

The ideal candidate has a strong understanding of Microsoft systems, excellent writing skills, and ... family medical history or genetic information, family or parental status, or any other status ...

Bausch & Lomb

OR · On-site

Prepare sales contracts that include terms, quotes, and pricing. * Administrative tasks include ... Strong communication skills, both written and oral communication * Ability to understand and ...

Attain Partners

OR · On-site

Strong negotiation, communication, and writing skills. * Ability to manage multiple priorities and ... Experience negotiating research agreements in a university, academic medical center, or research ...

LHH US

Contract Litigation Attorney

Portland, OR · On-site +1

$70/hr

Strong writing, analytical, and organizational skills * Ability to manage deadlines in a remote or ... Benefit offerings include medical, dental, vision, life insurance, short-term disability ...

LHH US

Contract Litigation Attorney

Portland, OR · On-site +1

$70/hr

Strong writing, analytical, and organizational skills * Ability to manage deadlines in a remote or ... Benefit offerings include medical, dental, vision, life insurance, short-term disability ...

Empower AI Inc.

... contract and the CERT program in general. Responsibilities: * Interacts with/presents to medical ... of written guidelines used by the CERT personnel. * Provides medical insight and expertise for ...

Empower AI Inc.

... contract and the CERT program in general. Responsibilities: * Interacts with/presents to medical ... of written guidelines used by the CERT personnel. * Provides medical insight and expertise for ...

Addus HomeCare

Assistant Medical Director

Salem, OR · On-site

$17.50 - $22.50/hr

Serenity Hospice is seeking a contract Physician for the PRN Assistant Medical Director role with ... Demonstrates excellent observation, problem solving, verbal and written communications. *Shows ...

Addus HomeCare

Assistant Medical Director

Salem, OR · On-site

$17.75 - $22.75/hr

Serenity Hospice is seeking a contract Physician for the PRN Assistant Medical Director role with ... Demonstrates excellent observation, problem solving, verbal and written communications. *Shows ...

Addus HomeCare

Assistant Medical Director

Salem, OR · On-site

$17.75 - $22.75/hr

Serenity Hospice is seeking a contract Physician for the PRN Assistant Medical Director role with ... Demonstrates excellent observation, problem solving, verbal and written communications. *Shows ...

Serenity Hospice

Assistant Medical Director

Salem, OR · On-site

$180 - $220/hr

Serenity Hospice is seeking a contract Physician for the Assistant Medical Director role with our ... Demonstrates excellent observation, problem solving, verbal and written communications. * Shows ...

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All JobsContract Medical Writing JobsContract Medical Writing Jobs in Oregon

Contract Medical Writing information

See Oregon salary details

$12

$48

$83

How much do contract medical writing jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for contract medical writing in Oregon is $48.92, according to ZipRecruiter salary data. Most workers in this role earn between $35.58 and $59.23 per hour, depending on experience, location, and employer.

What types of documents do contract medical writers typically work on, and how does the workflow usually look?

Contract medical writers commonly create regulatory submissions (such as clinical study protocols, investigator brochures, and clinical study reports), medical publications, and educational materials for healthcare professionals or regulatory authorities. The workflow usually begins with a project briefing, followed by extensive literature review, drafting, and rounds of review with subject matter experts, regulatory affairs, or clients. Most projects require frequent communication via email or virtual meetings and adherence to strict deadlines. Contract medical writers often work independently but must be flexible and responsive to feedback and changing priorities, which makes time management and adaptability crucial for success.

What is contract medical writing?

A Contract Medical Writing job involves creating regulatory, clinical, or scientific documents for pharmaceutical, biotech, or medical device companies on a contract or freelance basis. Medical writers in these roles develop documents such as clinical study reports, regulatory submissions, or scientific publications. They work independently or through agencies, often collaborating with researchers, clinicians, and regulatory teams. These roles offer flexibility in workload and project selection while requiring strong scientific knowledge and writing expertise.

What are the key skills and qualifications needed to thrive in contract medical writing, and why are they important?

To thrive as a Contract Medical Writer, you need a strong background in life sciences or pharmacy, excellent written communication skills, and experience with scientific or regulatory documentation. Familiarity with tools such as Microsoft Office Suite, reference management software, and guidelines like ICH, GCP, or AMA style, as well as relevant certifications (e.g., AMWA), is highly beneficial. Outstanding organization, time management, and the ability to communicate complex information clearly with diverse stakeholders will set you apart. These abilities ensure the creation of accurate, compliant medical documents and support effective collaboration in fast-paced, deadline-driven environments.

What are the most commonly searched types of Medical Writing jobs in Oregon? The most popular types of Medical Writing jobs in Oregon are:
What are popular job titles related to Contract Medical Writing jobs in Oregon? For Contract Medical Writing jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Contract Medical Writing jobs in Oregon look for? The top searched job categories for Contract Medical Writing jobs in Oregon are:
Contract Medical Writing jobs near you
Infographic showing various Contract Medical Writing job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $101,748 per year, or $48.9 per hour.

Senior Clinical Trial Manager (CTM)

Praxis Precision Medicines, Inc.

OR • On-site, Remote

Other

Re-posted 13 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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