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Research Associate Ii Jobs in Oregon (NOW HIRING)

PSI CRO

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on ... Must have 2+ years of independent on-site monitoring experience * Experience in all types of ...

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Clinical Research Associate II

Portland, OR

$91K - $114K/yr

Clinical Research Associate - Oncology - West Region ICON is a global healthcare intelligence and ... A clinical research professional with 2+ years of on-site monitoring experience in the ...

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Clinical Research Associate II

Portland, OR · Remote

Senior CRA / CRA II - United States - Home Based ICON is a global healthcare intelligence and ... Extensive experience as a Clinical Research Associate, with a strong understanding of clinical ...

OCHIN

Research Associate

Portland, OR · On-site +1

The Research Associate will provide professional, substantive, technical, and administrative ... At least 2 years of health-related research experience (degree or additional educational and ...

OCHIN

Research Associate

Portland, OR · On-site

The Research Associate will provide professional, substantive, technical, and administrative ... At least 2 years of health-related research experience (degree or additional educational and ...

OCHIN

Research Associate

Portland, OR · On-site +1

The Research Associate will provide professional, substantive, technical, and administrative ... At least 2 years of health-related research experience (degree or additional educational and ...

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All JobsResearch Associate Ii JobsResearch Associate Ii Jobs in Oregon

Research Associate Ii information

See Oregon salary details

$17

$34

$49

How much do research associate ii jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for research associate ii in Oregon is $34.41, according to ZipRecruiter salary data. Most workers in this role earn between $27.69 and $39.13 per hour, depending on experience, location, and employer.

What is a Research Associate II?

A Research Associate II is a mid-level research professional who assists in conducting experiments, collecting and analyzing data, and helping to manage research projects under the supervision of senior staff or principal investigators. They typically have more experience and responsibilities than entry-level research associates, often requiring a bachelor's or master's degree in a relevant field. Research Associate IIs may also contribute to writing reports, maintaining laboratory equipment, and ensuring compliance with safety and ethical guidelines.

How does a Research Associate II typically collaborate with other members of the research team?

As a Research Associate II, you will regularly collaborate with principal investigators, fellow research associates, laboratory technicians, and sometimes external partners. Your role often involves coordinating experiments, sharing data, and discussing results during team meetings to ensure project goals are met efficiently. Strong communication and teamwork skills are essential, as you'll be expected to both contribute your expertise and support others’ work within multi-disciplinary projects. This collaborative environment not only fosters professional growth but also enhances the quality and impact of the research.

What are the key skills and qualifications needed to thrive as a Research Associate II, and why are they important?

To thrive as a Research Associate II, you need a solid background in scientific research, data analysis, and relevant field-specific knowledge, typically supported by a bachelor's or master's degree. Experience with laboratory techniques, statistical software (such as SPSS or R), and compliance with research protocols is usually required. Strong problem-solving abilities, attention to detail, and effective communication skills help you collaborate and contribute to research projects. These competencies are crucial for ensuring the integrity, accuracy, and success of scientific studies.

What is the difference between Research Associate Ii vs Research Associate I?

AspectResearch Associate IiResearch Associate I
Required CredentialsBachelor's or Master's degree, some roles may prefer experienceBachelor's degree typically sufficient
Work EnvironmentLaboratory, research facilities, fieldworkLaboratory, research settings, similar to Research Associate II
Employer & Industry UsageAcademic, biotech, pharmaceutical, government researchSimilar industries, often entry-level or early career
Common Search & ComparisonHigher responsibility, more independent workEntry-level, foundational research tasks

The main difference between Research Associate II and Research Associate I lies in experience and responsibility. Research Associate II typically requires more experience or advanced education, allowing for greater independence and complex task management. Research Associate I is often an entry-level position with foundational research duties. Both roles are common in research-intensive industries like biotech, academia, and pharmaceuticals, but Research Associate II generally involves more advanced responsibilities.

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

The most popular types of Research Ii jobs in Oregon are:

What are popular job titles related to Research Associate Ii jobs in Oregon?

For Research Associate Ii jobs in Oregon, the most frequently searched job titles are:

What job categories do people searching Research Associate Ii jobs in Oregon look for?

The top searched job categories for Research Associate Ii jobs in Oregon are:

What cities in Oregon are hiring for Research Associate Ii jobs?

Cities in Oregon with the most Research Associate Ii job openings:

Research Associate Ii jobs near you
Infographic showing various Research Associate Ii job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $71,563 per year, or $34.4 per hour.

Regional Clinical Research Associate II

Biotronik

Lake Oswego, OR • On-site

Full-time

Re-posted 12 days ago

Key responsibilities

  • Conduct monitoring activities to evaluate protocol compliance, data accuracy, and subject safety through review of regulatory documents, medical records, reported data, and investigational device accountability.

  • Manage all monitoring responsibilities for assigned clinical studies, including scheduling visits, identifying discrepancies, communicating findings, and escalating issues.

  • Collaborate with investigators, research coordinators, and cross-functional teams to ensure compliance, address findings, and support study execution.

Job description

Regional Clinical Research Associate II
BIOTRONIK is one of the leading manufacturers of cardio- and endovascular implants and catheters for cardiac rhythm management, electrophysiology and vascular intervention. As a globally active company headquartered in Berlin, Germany, we develop, produce and distribute high-quality medical products based on the latest technology and research. Our success is based on the competence and results-oriented cooperation of our employees.
BIOTRONIK is looking to add a Regional Clinical Research Associate II to our Clinical Studies team. Conduct on-site, remote, and centralized monitoring to ensure compliance with FDA regulations, ICH/GCP guidelines, BIOTRONIK procedures, and IRB/EC policies. Supports clinical studies in cardiac rhythm management and related areas by ensuring data integrity, subject safety, and protocol adherence.
Your Responsibilities:
  • Conduct monitoring activities in accordance with BIOTRONIK procedures and applicable regulations to evaluate protocol compliance, data accuracy, and subject safety through review of regulatory documents, medical records, reported data, and investigational device accountability (as applicable).
  • Manage all monitoring responsibilities for assigned clinical studies, including:
    • Scheduling and completing monitoring visits within established timelines in alignment with risk-based monitoring plans and internal procedures.
    • Identifying data discrepancies and compliance issues; communicating findings to site staff, providing retraining where necessary, and developing effective resolution strategies.
    • Escalating significant issues to the study team and department management through appropriate channels, including monitoring visit reports.
  • Collaborate closely with Investigators and Research Coordinators during monitoring visits to ensure compliance, address findings, and support timely issue resolution.
  • Partner with BIOTRONIK Clinical Studies team members to prepare for site visits, proactively assess site performance, and escalate critical findings.
  • Present monitoring outcomes to site staff with clear guidance on corrective actions; review and resolve data queries to ensure mutual understanding and closure.
  • Serve as an ongoing resource to study sites between visits, providing guidance on data queries, action items, and study requirements.
  • Train and mentor BIOTRONIK staff on monitoring processes and best practices; conduct site training and co-monitoring visits as requested.
  • Complete all required documentation, including monitoring reports, follow-up letters, and action items, in accordance with BIOTRONIK standards.
  • Support departmental and study-related initiatives, including audits, investigator meetings, and training activities, in collaboration with the Manager, CRA Group.
  • Interface effectively with cross-functional teams, including Clinical, Regulatory, Sales, and site personnel, to support study execution.

Your Profile
  • Bachelor's degree or higher level degree in nursing, life sciences or related medical/scientific field.
  • Must have a valid US driver's license.
  • Minimum of 3 years on-site monitoring research experience for a CRO, Pharma, or Medical Device company. Experience supporting medical device IDE trials is preferred.
  • Strong clinical trial monitoring experience in relevant BIOTRONIK product and/or relevant therapeutic areas (electrophysiology and vascular interventional cardiology) preferred.
  • Demonstrated experience in clinical trial monitoring, preferably within electrophysiology, cardiology, or related therapeutic areas.
  • Experience monitoring first-in-human (FIH), investigational device exemption (IDE), post-approval, and/or post-market studies.
  • Strong understanding of GCP/ICH guidelines and FDA regulations, including 21 CFR Parts 11, 50, 54, 56, 812, and 820, as well as ISO standards for medical device clinical trials.
  • Current certification as a Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP).
    Solid knowledge of medical terminology.
  • Ability to work independently with minimal supervision in a regional territory.
  • Strong organizational, analytical, and problem-solving skills, with the ability to assess complex situations and develop effective solutions.
  • Excellent interpersonal and communication skills, with the ability to engage effectively with physicians, site staff, cross-functional teams, and leadership.
  • Ability to communicate protocol and regulatory requirements clearly and constructively.
  • Responsible for adequate and reasonable home office set up including dedicated desk space to accommodate work responsibilities and BIOTRONIK supplied equipment.

Travel
  • Approximately 75% travel required throughout the United States to investigational centers and BIOTRONIK, Inc. corporate office. Travel frequency may vary based on study needs and may include air, ground, or rail travel.

Location
  • Remote opportunity based in the Midwest, Southwest or Southeast

Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Midwest, southwest or Southeast, United States | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 62419 | BIOTRONIK Inc. | United States (US)
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. Please note that applications sent by post will only be returned if a sufficiently stamped self-addressed envelope is included.

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