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Clinical Study Manager Jobs in Bend, OR (NOW HIRING)

micro1 AI

Medical Writing Manager

Bend, OR · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Billing Specialist

Bend, OR · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

Rezolute

Sr. Director, Commercial Supply Chain

Bend, OR · On-site

$192K - $217K/yr

... new clinical studies. * Collaborate closely with the clinical supply leader to ensure comprehensive supply planning, risk management, and compliance with global GxP standards. * Ensure alignment ...

Specialtycare

EEG Technologist

Bend, OR · On-site

Under the clinical supervision of the Clinical Coordinator, Clinical Manager and NeuroCare Director perform electroneurodiagnostic studies and tasks at an advanced level due to extensive job ...

Specialy Care

EEG Technologist

Bend, OR · On-site

Under the clinical supervision of the Clinical Coordinator, Clinical Manager and NeuroCare Director perform electroneurodiagnostic studies and tasks at an advanced level due to extensive job ...

Stcharles

Sleep Lab Technician Day/Night

Bend, OR · On-site

$31.72 - $47.57/hr

Clinical Supervisor, RPSGT DEPARTMENT: St. Charles Sleep Center DATE LAST REVIEWED: July 2024 OUR ... Performs sleep study data acquisition for pediatric and adultPSGsaccording to ordering provider.

Stcharles

Sleep Lab Technician Day/Night

Redmond, OR · On-site

$31.72 - $47.57/hr

Clinical Supervisor, RPSGT DEPARTMENT: St. Charles Sleep Center DATE LAST REVIEWED: July 2024 OUR ... Performs sleep study data acquisition for pediatric and adultPSGsaccording to ordering provider.

genex

Field Nurse Case Manager (PT)

Bend, OR · On-site

$81K - $100K/yr

Uses clinical/nursing skills to help coordinate the individual's treatment program while ensuring ... Masters level and/or advanced study in a health-related field desired. EXPERIENCE: Minimum of two ...

genex

Field Nurse Case Manager (PT)

Bend, OR

$81K - $100K/yr

Uses clinical/nursing skills to help coordinate the individual's treatment program while ensuring ... Masters level and/or advanced study in a health-related field desired. EXPERIENCE: Minimum of two ...

Genex

Field Nurse Case Manager (PT)

Bend, OR · On-site

$81K - $100K/yr

Main responsibilities will include but are not limited to: • Uses clinical/nursing skills to help ... Masters level and/or advanced study in a health-related field desired. EXPERIENCE: Minimum of two ...

Rezolute

Head of Global Product Supply

Bend, OR · On-site

$245K - $257K/yr

Accountable for the current Plan of Record, inclusive of late phase clinical supply supporting two Phase 3 pivotal (global) studies in rare disease. Provides oversight, leadership and management as ...

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Clinical Study Manager information

See Bend, OR salary details

$30

$65

$101

How much do clinical study manager jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical study manager in Bend, OR is $65.95, according to ZipRecruiter salary data. Most workers in this role earn between $53.51 and $74.33 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.

How much does a clinical study manager earn?

A clinical study manager's salary varies based on experience, location, and the size of the organization, but typically ranges from $80,000 to $130,000 annually. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. The position often requires knowledge of regulatory guidelines and project management tools.

What does a clinical study manager do?

A clinical study manager oversees the planning, execution, and monitoring of clinical trials to ensure they comply with regulatory standards and protocols. They coordinate with research teams, manage timelines and budgets, and ensure data quality, often using specialized software and requiring knowledge of Good Clinical Practice (GCP) guidelines.

What are popular job titles related to Clinical Study Manager jobs in Bend, OR?

For Clinical Study Manager jobs in Bend, OR, the most frequently searched job titles are:

What job categories do people searching Clinical Study Manager jobs in Bend, OR look for?

The top searched job categories for Clinical Study Manager jobs in Bend, OR are:

What cities near Bend, OR are hiring for Clinical Study Manager jobs?

Cities near Bend, OR with the most Clinical Study Manager job openings:

Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Bend, OR as of August 2026, with employment types broken down into 83% Full Time, 16% Part Time, and 1% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $137,186 per year, or $66 per hour.

Medical Writer / Clinical Document Author

micro1 AI

Bend, OR • Remote

$50 - $80/hr

Part-time

Re-posted 2 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply