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Clinical Trials Associate Jobs in Oregon (NOW HIRING)

Natera

OR · On-site

Natera is seeking an Associate Director/Sr. Manager, Business Development to lead and expand our ... clinical trials, real-world evidence, and companion diagnostics. Responsibilities: Strategic ...

410 ICR United States USA

CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and analyzing clinical trials ...

Icon plc

CRA II and Senior CRA

Portland, OR · Remote

$91K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Clinical Research Associate (Level II or Senior) to join our diverse and dynamic team. As a CRA II/Senior CRA at ICON, you will play a pivotal role in designing and analyzing clinical trials ...

Suvoda

Associate Project Manager

Portland, OR · On-site

We are seeking an entry-level, analytically-oriented Associate Project Manager to join our team ... clinical trials * Support the Services Delivery project team in: * Liaising with the client to ...

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Clinical Trials Associate information

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$42

$74

How much do clinical trials associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical trials associate in Oregon is $42.28, according to ZipRecruiter salary data. Most workers in this role earn between $34.04 and $46.49 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems; certifications like CCRP can be advantageous.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

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

The most popular types of Clinical Trials jobs in Oregon are:

What cities in Oregon are hiring for Clinical Trials Associate jobs?

Cities in Oregon with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Oregon as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 18% Part Time, 7% Contract, and 1% Nights. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $87,934 per year, or $42.3 per hour.

Associate Director/Sr. Manager Business Development

Natera

OR • On-site

Full-time

Re-posted 3 days ago

Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

59th of 120 rated laboratories

Job description

Natera is seeking an Associate Director/Sr. Manager, Business Development to lead and expand our biopharma partnerships within the Organ Health area. This strategic role requires a proven track record of cultivating partnerships across the life sciences industry. The ideal candidate will bring deep knowledge of the drug development lifecycle, from discovery through commercialization, and experience structuring deals involving clinical trials, real-world evidence, and companion diagnostics.

 

Responsibilities:

    Strategic Partnering & Business Development Leadership

o   Identify, initiate, and manage strategic partnerships with pharmaceutical, biotech, and technology companies.

o   Lead cross-functional deal teams from initial outreach through contract execution.

o   Own and develop long-term strategic plans for partnership growth in line with company goals.

o   Drive evaluation of new business models, including risk-sharing partnerships and platform collaborations.

        Market Intelligence & Opportunity Assessment

o   Provide thought leadership on emerging trends in drug development, clinical trials, precision medicine, and diagnostics.

o   Analyze partner pipelines, market needs, and whitespace to inform opportunity prioritization.

o   Present insights and recommendations to executive leadership and influence company strategy.

        Deal Structuring & Execution

o   Lead negotiations and structuring of complex business development deals, including research collaborations, licensing, and co-commercialization.

o   Partner with legal, finance, and regulatory stakeholders to structure compliant and value-driven agreements.

        Stakeholder Engagement & Representation

o   Represent Natera at key industry meetings, conferences, and partner events to build credibility and relationships.

o   Serve as a trusted liaison to external partners, internal leadership, and cross-functional teams.

Qualifications:

        Bachelor's degree in Life Sciences, Business, or a related field; MBA or advanced scientific degree strongly preferred.

        5+ years of experience in business development, corporate strategy, or alliance management within biopharma, diagnostics, or healthcare technology.

        Demonstrated success in sourcing, negotiating, and closing high-value partnerships.

        Deep understanding of the drug development ecosystem, including clinical trial design, regulatory pathways, and commercialization.

        Exceptional communication, negotiation, and stakeholder management skills.

        Strategic thinker with strong analytical and financial modeling capabilities.

        Proficiency in CRM tools (e.g., Salesforce) and business tools (PowerPoint, Excel).

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