1

Clinical Research Project Manager Jobs in Oregon

... research projects in a variety of therapeutic indications. You will build and maintain ... Be responsible for site communication and management * Supervise study activities, timelines, and ...

next page

Showing results 1-20

Clinical Research Project Manager information

See Oregon salary details

$52.9K

$91K

$139.6K

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

As of Sep 1, 2026, the average yearly pay for clinical research project manager in Oregon is $90,960.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $96,700.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

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

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

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

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Project jobs in Oregon?

The most popular types of Clinical Research Project jobs in Oregon are:

What are popular job titles related to Clinical Research Project Manager jobs in Oregon?

For Clinical Research Project Manager jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Clinical Research Project Manager jobs in Oregon look for?

The top searched job categories for Clinical Research Project Manager jobs in Oregon are:

What cities in Oregon are hiring for Clinical Research Project Manager jobs?

Cities in Oregon with the most Clinical Research Project Manager job openings:

Infographic showing various Clinical Research Project Manager job openings in Oregon as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $90,960 per year, or $43.7 per hour.

Project Manager, Clinical Research - New Site Build

MD Ally

Dallas, OR โ€ข On-site

$80 - $110/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago


Job description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

As the Project Manager, Clinical Research โ€“ New Site Build at Iterative Health for the Cardiology service line, you will lead the end-to-end execution of opening new Cardiology research sites from the ground up.Reporting to the VP, Growth, you will serve as the central project leader responsible for coordinating every aspect of a new site's developmentโ€”from site selection and facility readiness through regulatory activation, staffing, technology implementation, and study launch. Working cross functionally you\'ll ensure each site is delivered on time, on budget, and fully prepared to enroll patients.This role is ideal for an experienced project manager who enjoys building new programs, thrives in highly cross-functional environments, and is passionate about expanding patient access to innovative cardiovascular clinical trials.Where You'll Drive Impact
  • Lead the end-to-end project management of de novo Cardiology clinical research site development, from approval through operational launch.
  • Develop and manage comprehensive project plans, timelines, milestones, budgets, and risk registers for each new site.
  • Coordinate cross-functional workstreams across Clinical Operations, Regulatory, Legal, Finance, Real Estate, Facilities, IT, HR, Procurement, and Business Development.
  • Partner with Real Estate and Facilities teams to ensure new sites are designed, built, and equipped to support high-quality clinical research operations.
  • Oversee site activation activities including licensing, regulatory readiness, technology implementation, equipment procurement, SOP deployment, and operational workflows.
  • Coordinate recruiting timelines and onboarding activities with Human Resources to ensure appropriate staffing prior to site launch.
  • Partner with Clinical Operations leadership to establish study startup readiness, investigator onboarding, and research staff training.
  • Identify project risks, dependencies, and operational challenges while proactively developing mitigation plans to maintain timelines.
  • Facilitate regular cross-functional project meetings and provide executive-level status updates to leadership.
  • Develop standardized playbooks, templates, and project management tools to support scalable expansion across future de novo sites.
  • Monitor project budgets, resource allocation, and vendor performance throughout the site development lifecycle.
  • Support continuous process improvement initiatives to enhance speed, consistency, and quality of future site launches.
  • Perform other duties as assigned.
What You Bring to the Team
  • Bachelor\'s degree in Healthcare Administration, Life Sciences, Business, Project Management, or a related field.
  • 5โ€“8+ years of project management experience within healthcare, clinical research, life sciences, healthcare operations, or healthcare facility development.
  • Experience leading large, cross-functional initiatives involving multiple stakeholders and competing priorities.
  • Strong organizational and project management skills with exceptional attention to detail.
  • Proven ability to manage multiple complex projects simultaneously while meeting aggressive timelines.
  • Excellent communication, presentation, and stakeholder management skills.
  • Experience developing project plans, tracking milestones, managing budgets, and reporting project performance.
  • Ability to influence cross-functional teams without direct authority.
  • Highly adaptable with strong problem-solving and decision-making skills.
  • Comfortable working in a fast-paced, rapidly growing organization.
Preferred Qualifications
  • Experience launching new healthcare facilities, physician practices, ambulatory care centers, or clinical research sites.
  • Experience within Cardiology clinical research or cardiovascular healthcare.
  • Knowledge of clinical trial startup, GCP, FDA regulations, and site activation processes.
  • PMP certification or equivalent project management certification.
  • Experience with Smartsheet, Monday.com, Asana, Microsoft Project, or similar project management platforms.
  • Familiarity with CTMS, eRegulatory systems, and clinical research technologies.
How We Work
  • Collaborative and low-ego team environment
  • High ownership and accountability culture
  • Fast-paced and highly iterative growth environment
  • Open communication and continuous learning mindset
  • Mission-driven organization focused on improving patient outcomes
  • Comfortable navigating evolving business priorities and opportunities
Benefits That Support You

We believe great teams do their best work when they feel supported โ€” professionally and personally.

  • Hybrid work environment with in-office collaboration two days per week in either our NYC or Boston office
  • Comprehensive medical, dental, and vision coverage, with up to 80% of premiums covered by Iterative Health
  • Mental health and wellness support through Spring Health
  • Health HSA or FSA options, and commuter FSA contributions supported by Iterative Health
  • Unlimited PTO, 12 company holidays, and a company-wide shutdown between Christmas and New Years
  • 401(k) program with a company match of up to 3% (up to $3,000 annually)
  • Weekly in-office lunch benefit every Tuesday
  • 100% company-paid short-term and long-term disability coverage
  • Annual wellness and professional development stipend to support your health and growth
  • And more!

New York pay range

$80,000 โ€” $110,000 USD

At Iterative Health, weโ€™re actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

#J-18808-Ljbffr