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Manager Pfizer Clinical Research Jobs in Remote, OR

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:

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:

IT ENGAGEMENTS INC

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CGM Statistician (Contract Role)

OR · On-site

$65 - $70/hr

Collaborate with clinical, data management, and programming teams. Requirements: * Experience as a Statistician/Biostatistician in clinical research. * Experience working with Continuous Glucose ...

IT ENGAGEMENTS INC

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CGM Statistician (Contract Role)

OR · On-site

$65 - $70/hr

Collaborate with clinical, data management, and programming teams. Requirements: * Experience as a Statistician/Biostatistician in clinical research. * Experience working with Continuous Glucose ...

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 ...

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All JobsPfizer Clinical Research JobsManager Pfizer Clinical Research JobsManager Pfizer Clinical Research Jobs in Remote, OR

Manager Pfizer Clinical Research information

See Remote, OR salary details

$49K

$107.2K

$188.8K

How much do manager pfizer clinical research jobs pay per year?

As of Sep 8, 2026, the average yearly pay for manager pfizer clinical research in Remote, OR is $107,230.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,900.00 and $122,400.00 per year, depending on experience, location, and employer.
Manager Pfizer Clinical Research jobs near you
Infographic showing various Manager Pfizer Clinical Research job openings in Remote, OR as of August 2026, with employment types broken down into 87% Full Time, 10% Part Time, and 3% Contract. Highlights an 69% Physical, 2% Hybrid, and 29% Remote job distribution, with an average salary of $107,230 per year, or $51.6 per hour.

Senior Clinical Research Associate

Nexpro Technologies Inc

OR • Remote

$90K - $120K/yr

Full-time

Medical

Re-posted 1 hour 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.