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Associate Director Validation Jobs in Oregon (NOW HIRING)

As an Associate Director in Biostatistics, you will leverage your deep applied statistics and ... Oversee Biostatistics contributions to oncology product clinical validation projects * Lead ...

POSITION SUMMARY: We are seeking an Associate Director, Clinical Science to architect trial ... This clinical leadership role shapes the data validation pipeline for our cell-free DNA (cfDNA ...

The Associate Director, Medical Review & Training serves as the medical subject matter expert for ... valid, balanced, and supported by appropriate evidence * Evaluate clinical data, literature, and ...

The Neurology Associate Director, Thought Leader Liaison (TLL) is a field-based, non-sales position ... Must have a valid driver's license * Must be able to travel 60%-80% of time Does this sound like ...

OR · On-site

The Associate Medical Director, Genitourinary Oncology is a critical leadership role responsible ... minimum validation requirements. * Provide post-launch medical affairs support, including ...

Responsibilities will span from overcoming objections to validating client information and managing ... Additionally, the Associate Loan Originator will undertake preparation for the National Uniform ...

... Associate Director or Director, Partner Development (candidates are being considered across all ... Valid driver's license * Professional experience in at least three of the following: * Corporate ...

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Associate Director Validation information

How does an Associate Director of Validation typically collaborate with cross-functional teams during major projects?

An Associate Director of Validation works closely with departments such as Quality Assurance, Manufacturing, Engineering, and Regulatory Affairs to ensure that validation activities meet both internal standards and regulatory requirements. This often involves leading multi-disciplinary project teams, facilitating communication, and resolving challenges related to process or equipment validation. Regular meetings, joint risk assessments, and coordinated documentation are common, which helps streamline project timelines and maintain compliance. Effective collaboration is essential for successful product launches and ongoing process improvements.

What is the difference between Associate Director Validation vs Validation Manager?

AspectAssociate Director ValidationValidation Manager
CredentialsBachelor's or Master's in Life Sciences, Engineering, or related fields; often requires industry certificationsBachelor's or Master's in similar fields; certifications like ASQ or ISPE are common
Work EnvironmentLeads validation teams, oversees validation strategies, and collaborates with cross-functional departmentsManages validation projects, ensures compliance, and reports to senior management
Employer & Industry UsagePharmaceutical, biotech, and medical device industries; used in large organizationsSimilar industries; common in mid to large-sized companies for validation oversight

The Associate Director Validation typically holds a higher strategic role, overseeing validation teams and strategies, while the Validation Manager focuses on managing validation projects and ensuring compliance. Both roles require similar credentials and are vital in regulated industries, but the Associate Director has broader leadership responsibilities.

What are the key skills and qualifications needed to thrive as an Associate Director Validation, and why are they important?

To excel as an Associate Director Validation, you need in-depth knowledge of validation principles, regulatory guidelines (such as FDA, EMA), and a background in life sciences or engineering, often supported by advanced degrees. Familiarity with validation software, quality management systems (QMS), and industry-standard protocols like GAMP or ASTM E2500 is crucial. Strong leadership, project management, and cross-functional communication skills help drive teams and ensure compliance. These competencies are essential to maintain product quality, regulatory adherence, and efficient validation processes in a highly regulated environment.

What is an Associate Director of Validation?

An Associate Director of Validation is a leadership role in the pharmaceutical, biotechnology, or medical device industries responsible for overseeing validation activities. This includes ensuring that equipment, processes, and systems meet regulatory standards and function as intended. The Associate Director manages validation teams, develops validation strategies, and ensures compliance with industry regulations such as FDA and GMP. They play a key role in quality assurance and help maintain the integrity of products and processes.
What are popular job titles related to Associate Director Validation jobs in Oregon? For Associate Director Validation jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Associate Director Validation jobs in Oregon look for? The top searched job categories for Associate Director Validation jobs in Oregon are:
What cities in Oregon are hiring for Associate Director Validation jobs? Cities in Oregon with the most Associate Director Validation job openings:

Associate Director of Biostatistics

Natera

OR

Other

Posted 2 days ago


Natera rating

7.7

Company rating: 7.7 out of 10

Based on 35 frontline employees who took The Breakroom Quiz

50th of 103 rated laboratories


Job description

This is an exciting opportunity to lead a team of statisticians advancing adoption of Natera's oncology portfolio of cutting-edge molecular diagnostic tests. As an Associate Director in Biostatistics, you will leverage your deep applied statistics and leadership background to guide the design and interpretation of Natera sponsored clinical studies ensuring scientific rigor and meaningful clinical insights across oncology programs.  This position will play a central role in defining the team's vision, fostering excellence in biostatistics deliverables, and cultivating a high-performing, collaborative environment that drives long-term success.

PRIMARY RESPONSIBILITIES: 

  • Direct a team of biostatisticians, taking responsibility for their individual deliverables and growth (technical and professional) 

  • Oversee Biostatistics contributions to oncology product clinical validation projects

  • Lead development of novel statistical approaches and simulations to support innovative study designs.

  • Produce, review, and standardize high-quality documentation for cross-functional internal and external collaborators and stakeholders 

  • Identify risks, communicate concerns, and champion solutions to cross-functional project teams 

  • Continuously improve the efficiency and efficacy of team through innovative techniques and strategies

QUALIFICATIONS: 

  • Advanced degree (Ph.D. or M.S.) in Biostatistics, Statistics, or a related quantitative field (Ph.D. preferred)

  • 7+ years of experience in clinical trial biostatistics

  • Strong knowledge of survival analysis, censoring, and other advanced statistical techniques relevant to oncology

  • Expertise with study design innovation and power/simulation approaches

  • Proven track record in mentoring and developing junior staff 

  • Ability to communicate complex statistical concepts clearly to both technical and non-technical audiences and foster collaborative, cross-functional partnerships

KNOWLEDGE, SKILLS, AND ABILITIES: 

  • Strong technical leadership and strategic thinking.

  • Proven success leading and developing teams.

  • Deep expertise in statistical methods for diagnostics and clinical trials, including FDA requirements.

  • Effective collaborator across diverse technical disciplines.

  • Clear, high-quality scientific and technical communication.

  • Familiarity with NGS, ctDNA, and molecular oncology preferred.


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