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Preclinical Research Associate Jobs in Oregon (NOW HIRING)

Job Overview *May be filled at the Associate Director level based on experience. The Medical ... Present and interpret complex cardiovascular clinical data (Preclinical research, Phase I-IV, ...

Preclinical Research Associate information

What is the difference between Preclinical Research Associate vs Laboratory Technician?

AspectPreclinical Research AssociateLaboratory Technician
Required CredentialsBachelor's degree in life sciences; some roles may require experience in researchAssociate's degree or relevant certification; entry-level
Work EnvironmentResearch labs in biotech/pharmaceutical companies; clinical trial settingsLaboratories performing routine tests and experiments
Employer & Industry UsageUsed in biotech, pharma, and research institutions for drug developmentCommon in clinical labs, hospitals, and research facilities
Comparison Search IntentUnderstanding research roles in drug developmentLearning about lab support roles in scientific settings

The Preclinical Research Associate and Laboratory Technician roles both work within laboratory environments, but the associate typically engages in more complex research activities related to drug development, requiring a higher level of education and specialized knowledge. The technician role focuses on routine lab tasks and support functions. Both positions are essential in scientific research, but they differ in responsibilities and career progression.

What are the key skills and qualifications needed to thrive as a preclinical research associate?

A Preclinical Research Associate needs a solid background in life sciences, laboratory techniques, and data analysis, typically supported by a bachelor's degree in biology, pharmacology, or a related field. Familiarity with laboratory information management systems (LIMS), animal handling protocols, and regulatory standards such as GLP is often required. Strong attention to detail, problem-solving abilities, and effective teamwork are valuable soft skills in this role. These competencies are essential to ensure accurate experimental results, compliance with research regulations, and effective collaboration within research teams.

What are some common challenges faced by preclinical research associates and how can they be managed?

Preclinical Research Associates often encounter challenges such as managing tight project timelines, adapting to evolving experimental protocols, and ensuring strict adherence to regulatory guidelines. Balancing multiple studies simultaneously can require strong organizational and communication skills, especially when collaborating with cross-functional teams like scientists, veterinarians, and data analysts. Staying proactive in seeking feedback, participating in regular team meetings, and consistently documenting experimental procedures help manage these challenges and ensure high-quality results.

What is a preclinical research associate?

Preclinical Research Associates are professionals who support scientific studies that evaluate the safety and efficacy of new drugs, medical devices, or treatments before they are tested in humans. They are responsible for conducting laboratory experiments, collecting and analyzing data, and ensuring compliance with regulatory standards. Their work is crucial for identifying potential risks and optimizing study protocols, laying the groundwork for clinical trials. Preclinical Research Associates typically work in pharmaceutical companies, biotechnology firms, or academic research settings, collaborating closely with scientists and regulatory teams.
What are the most commonly searched types of Preclinical Research jobs in Oregon? The most popular types of Preclinical Research jobs in Oregon are:
What are popular job titles related to Preclinical Research Associate jobs in Oregon? For Preclinical Research Associate jobs in Oregon, the most frequently searched job titles are:
Infographic showing various Preclinical Research Associate job openings in Oregon as of August 2026, with employment types broken down into 100% Full Time. Highlights an 50% In-person, and 50% Remote job distribution.

Director, Field Medical/Medical Science Liaison -Mountain

Kardigan

OR

Full-time

Posted 6 days ago


Job description

Job Overview 

*May be filled at the Associate Director level based on experience.

The Medical Science Liaison (MSL) serves as a field-based scientific leader responsible for advancing the medical strategy within a defined territory.

The individual acts as a scientific expert in cardiovascular disease (e.g., heart failure, cardiomyopathies, hypertension, cardiometabolic disease, etc.), builds trusted partnerships with key opinion leaders (KOLs), and implements the Cardiovascular Medical Strategy locally. 

Essential Duties and Responsibilities 

Scientific Engagement & KOL Development

  • Develop and maintain strategic peer-to-peer relationships with leading cardiologists, heart failure specialists, interventionalists, and academic researchers. 
  • Conduct high-level scientific exchange regarding disease state, mechanism of action, clinical trial data, real-world evidence, and emerging pipeline assets.
  • Identify opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact within the assigned territory.
  • Present and interpret complex cardiovascular clinical data (Preclinical research, Phase I-IV, biomarker data).
  • Identify unmet needs and evolving trends within cardiovascular treatment paradigms.
  • Support national and local medical congresses (ACC, AHA, ESC, HFSA) through scientific engagement and insight capture.
  • Capture actionable medical insights from external experts in support of medical strategy.

Clinical & Research Support

  • Provide clinical trial support for company sponsored trials, facilitating relevant medical activities and working cross-functionally with Medical Affairs and Clinical Operations colleagues.
  • Provide protocol education and scientific support in compliance with regulations.
  • Support site feasibility, trial enrollment acceleration, and retention strategies.
  • Facilitate investigator-initiated studies (IIS) and research collaborations, as appropriate.

Compliance & Governance

  • Ensure all scientific interactions comply with FDA, EMA, Sunshine Act, and internal SOPs.
  • Maintain accurate documentation of all field activities in CRM systems.
  • Uphold ethical standards and scientific integrity in all engagements. 

Qualifications and Preferred Skills 

Education 

  • MD, PharmD, PhD, or equivalent advanced scientific degree required.  

Experience 

  • 3+ years experience in cardiovascular Medical Affairs, clinical research, or related field.
  • Deep knowledge of cardiology, cardiovascular trials, treatment landscape, and guideline development. 
  • Prior MSL experience strongly preferred.

Expertise Areas May Include 

  • Heart Failure
  • Dilated and Hypertrophic Cardiomyopathy
  • Hypertension
  • Valvular Heart Diseases (Aortic Stenosis)
  • ASCVD & Lipid Disorders
  • Thrombosis & Anticoagulation
  • Cardiometabolic Disease
  • Rare Cardiovascular Conditions 

Anticipated travel (overnight/day) 60% -70%

Salary range posted is for MD's -Exact Compensation may vary based on skills, experience and location.