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Freelance Clinical Data Manager Jobs in Remote, OR

Aviva Health

Clinical Quality Manager

Roseburg, OR · On-site

$38.83 - $61.85/hr

This individual will review data, evaluate trends, and compare with benchmark measures. The Clinical Quality Manager may recommend actions based on the review and participate in the actions taken to ...

Aviva Health

Clinical Quality Manager

Roseburg, OR · On-site

$38.83 - $61.85/hr

This individual will review data, evaluate trends, and compare with benchmark measures. The Clinical Quality Manager may recommend actions based on the review and participate in the actions taken to ...

Aviva Health

Clinical Quality Manager

Roseburg, OR · On-site

$38.83 - $61.85/hr

This individual will review data, evaluate trends, and compare with benchmark measures. The Clinical Quality Manager may recommend actions based on the review and participate in the actions taken to ...

Bausch+Lomb Companies Inc.

Director, Clinical Development

OR · Remote

$81K - $111K/yr

Manage budgets and resources. * Ensure timely submission of clinical trial data to regulatory authorities. * Identify and mitigate risks associated with clinical research activities. Requirements:

Bausch + Lomb

Director, Clinical Development

OR · On-site +1

$75K - $102K/yr

Manage budgets and resources. * Ensure timely submission of clinical trial data to regulatory authorities. * Identify and mitigate risks associated with clinical research activities. Requirements:

Ottobock

Clinical Specialist (Orthotics - PCS)

OR · Remote

$105K - $115K/yr

Strong project management and organizational skills * Ability to manage multiple priorities and ... S. Compensation Data Salary Disclosure: $105,000-$115,000 base salary, plus bonus eligibility.

Ottobock

Clinical Specialist (Orthotics - PCS)

OR · On-site +1

$105K - $115K/yr

Strong project management and organizational skills * Ability to manage multiple priorities and ... S. Compensation Data Salary Disclosure: $105,000-$115,000 base salary, plus bonus eligibility.

Medsource Consultants

Physician

Coos Bay, OR

Interpret and integrate clinical data to determine diagnosis and therapeutic plans * Review and ... Administer and manage prescribed medications in compliance with state law and practice guidelines

Servier

Senior Manager, Privacy (Legal)

OR · On-site +1

$160 - $180K/hr

Key cross functional partners may include Patient Services, Patient Advocacy, Data Management, IT, HR, Legal, Clinical, R&D, Market Research, Commercial Marketing, and Commercial Operations This ...

AGFA

Service Innovation Manager

OR · On-site +1

... data management. From product development to implementation, our unified Enterprise Imaging Platform is purpose-built to reduce complexity, improve productivity and deliver clinical value. We use our ...

Agfa

Service Innovation Manager

OR · Remote

... data management. From product development to implementation, our unified Enterprise Imaging Platform is purpose-built to reduce complexity, improve productivity and deliver clinical value. We use our ...

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Freelance Clinical Data Manager information

See Remote, OR salary details

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How much do freelance clinical data manager jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for freelance clinical data manager in Remote, OR is $57.11, according to ZipRecruiter salary data. Most workers in this role earn between $45.14 and $67.98 per hour, depending on experience, location, and employer.

What does a freelance clinical data manager do?

A Freelance Clinical Data Manager is responsible for overseeing the collection, organization, and validation of clinical trial data on a project-by-project basis. They ensure that data is accurate, complete, and compliant with regulatory standards. Working independently or with contract research organizations, they develop data management plans, set up databases, and perform quality checks throughout the trial lifecycle. Their work is essential for ensuring that clinical study results are reliable and ready for regulatory submission.

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

To thrive as a Freelance Clinical Data Manager, you need expertise in clinical data management, database design, and regulatory standards, often backed by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems like Medidata Rave, CDISC standards, and GCP compliance is typically required, and certifications such as CCDM can be advantageous. Strong organizational skills, attention to detail, and the ability to communicate effectively with cross-functional teams set top performers apart. These skills ensure the integrity, accuracy, and regulatory compliance of clinical trial data, which is critical for successful study outcomes.

What are some common challenges faced by freelance clinical data managers when working with multiple clients?

Freelance clinical data managers often juggle projects for different clients, which can lead to challenges such as managing varied data management systems, adhering to diverse protocols, and aligning with multiple teams' workflows. Effective communication and organization are essential, as each client may have unique expectations, timelines, and regulatory requirements. Staying updated with industry standards and maintaining clear documentation can help overcome these challenges while ensuring high-quality deliverables.

What are popular job titles related to Freelance Clinical Data Manager jobs in Remote, OR?

For Freelance Clinical Data Manager jobs in Remote, OR, the most frequently searched job titles are:

What job categories do people searching Freelance Clinical Data Manager jobs in Remote, OR look for?

The top searched job categories for Freelance Clinical Data Manager jobs in Remote, OR are:

Freelance Clinical Data Manager jobs near you
Infographic showing various Freelance Clinical Data Manager job openings in Remote, OR as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $118,791 per year, or $57.1 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Re-posted 26 days ago

Job description

We are seeking a detail-oriented and motivated Clinical Research Associate (CRA) to oversee and monitor clinical trials while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. The ideal candidate will have experience in site monitoring, clinical trial management, and maintaining high-quality clinical data.

Key Responsibilities

  • Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines.
  • Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and Close-Out Visits (COV).
  • Verify source data and ensure data accuracy, integrity, and completeness.
  • Maintain Trial Master File (TMF) and essential study documentation.
  • Build and maintain strong relationships with investigators and site staff.
  • Identify, document, and resolve protocol deviations and study-related issues.
  • Ensure timely reporting of adverse events (AEs) and serious adverse events (SAEs).
  • Review informed consent documentation and ensure participant safety.
  • Prepare monitoring visit reports and follow-up letters.
  • Coordinate with Clinical Operations, Data Management, Biostatistics, Medical Writing, and Regulatory teams.
  • Support study start-up, patient recruitment, and site management activities.
  • Ensure studies are completed within timelines and quality standards.

Required Qualifications

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field.
  • 2–6 years of experience as a Clinical Research Associate in clinical trials.
  • Strong knowledge of ICH-GCP, FDA, EMA, and local regulatory requirements.
  • Experience with EDC systems, CTMS, and eTMF platforms.
  • Excellent communication, documentation, and organizational skills.
  • Willingness to travel for site monitoring visits.

Preferred Skills

  • Clinical site monitoring experience across multiple therapeutic areas.
  • Knowledge of protocol review, source document verification (SDV), and risk-based monitoring.
  • Strong analytical and problem-solving abilities.
  • Ability to manage multiple studies simultaneously and work independently.

Benefits

  • Competitive salary and performance incentives.
  • Health insurance and employee wellness programs.
  • Learning and career development opportunities.
  • Collaborative and supportive work environment.

Company Description

NexPro Technologies offers robust, responsive and value-driven IT consulting and placement services.