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Associate Director Clinical Operations Jobs in Bothell, WA

Immunome, Inc.

Clinical Trial Associate

Bothell, WA

$37.50 - $51.25/hr

Position Overview Immunome is seeking a Clinical Trial Associate (CTA) to support the operational ... Participate in the data cleaning activities as directed by Clinical Operations Manager. Vendor and ...

Uw

Radiology Clinical Operations Manager

Seattle, WA

$41.50 - $56.50/hr

... Clinical Operations Manager. WORK SCHEDULE * Full-Time / 40 Hours per Week * Day Shift POSITION ... Under the guidance of the Assistant Director and Director, models leadership in accordance with ...

Immunome, Inc.

Clinical Trial Associate

Bothell, WA · On-site

$37.50 - $51.25/hr

Position Overview Immunome is seeking a Clinical Trial Associate (CTA) to support the operational ... Participate in the data cleaning activities as directed by Clinical Operations Manager. Vendor and ...

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All JobsAssociate Clinical Operations JobsAssociate Director Clinical Operations JobsAssociate Director Clinical Operations Jobs in Bothell, WA

Associate Director Clinical Operations information

See Bothell, WA salary details

$68.2K

$165.9K

$321.1K

How much do associate director clinical operations jobs pay per year?

As of Jul 19, 2026, the average yearly pay for associate director clinical operations in Bothell, WA is $165,929.00, according to ZipRecruiter salary data. Most workers in this role earn between $115,900.00 and $197,200.00 per year, depending on experience, location, and employer.

How does an Associate Director of Clinical Operations typically collaborate with cross-functional teams during a clinical trial?

An Associate Director of Clinical Operations regularly works alongside teams such as Regulatory Affairs, Data Management, Medical Affairs, and Biostatistics to ensure trials run smoothly and meet compliance standards. They coordinate project timelines, facilitate communication between departments, and address operational challenges as they arise. This collaborative approach helps to streamline decision-making, resolve issues quickly, and keep the clinical trial on track for successful completion.

What does an Associate Director of Clinical Operations do?

An Associate Director of Clinical Operations oversees the planning, execution, and management of clinical trials within a pharmaceutical, biotechnology, or medical device company. They supervise clinical project teams, ensure regulatory compliance, manage budgets and timelines, and collaborate with cross-functional departments to deliver high-quality results. Their role is crucial in ensuring that clinical studies are conducted efficiently, safely, and in accordance with all applicable guidelines and standards.

What is the difference between Associate Director Clinical Operations vs Clinical Project Manager?

AspectAssociate Director Clinical OperationsClinical Project Manager
ResponsibilitiesOversees multiple clinical trials, manages teams, and ensures regulatory complianceManages individual clinical projects, coordinates activities, and tracks progress
Required CredentialsBachelor's or higher in life sciences, often with experience in clinical operationsBachelor's in life sciences, with project management experience
Work EnvironmentSenior-level role within clinical operations teams, often in biotech or pharma companiesProject-focused role, working closely with cross-functional teams in clinical settings

The Associate Director Clinical Operations typically oversees multiple clinical trials and manages teams, requiring broader strategic oversight. In contrast, a Clinical Project Manager focuses on managing specific projects, ensuring timely execution. Both roles require relevant clinical experience, but the Associate Director role involves higher-level leadership and operational responsibilities.

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

To thrive as an Associate Director Clinical Operations, you need expertise in clinical trial management, regulatory compliance, and strong leadership, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and project management tools is essential, along with relevant certifications like PMP or ACRP. Exceptional communication, problem-solving, and team-building skills enable effective cross-functional collaboration and decision-making. These skills are vital for ensuring the successful planning, execution, and oversight of clinical trials while meeting regulatory and organizational goals.
What job categories do people searching Associate Director Clinical Operations jobs in Bothell, WA look for? The top searched job categories for Associate Director Clinical Operations jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Associate Director Clinical Operations jobs? Cities near Bothell, WA with the most Associate Director Clinical Operations job openings:
Associate Director Clinical Operations jobs near you
Mfg Operations Associate Director - Biologics, Drug Substance

Mfg Operations Associate Director - Biologics, Drug Substance

Vertex Pharmaceuticals

Seattle, WA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

Job Description
General Summary:
The Associate Director, Technical Services is accountable for the technical execution of biologics drug substance manufacturing at external manufacturing partners.
This role is responsible for ensuring processes are executed as intended and delivering reliable supply. The Associate Director serves as the technical leader for manufacturing execution, driving performance, standardization, and rapid issue resolution across programs and CDMOs.
The Associate Director, Technical Services role is a key member of Vertex's External Manufacturing Organization (ExM), providing support, strategic insights and enterprise thinking to the Biopharmaceutical Sciences and Manufacturing Operations organization (BSMO).
The Associate Director, Technical Services is accountable for the technical execution of biologics drug substance manufacturing at external manufacturing partners. This role is responsible for ensuring processes are executed as intended and delivering reliable supply. The Associate Director serves as the technical leader for manufacturing execution, driving performance, standardization, and rapid issue resolution across programs and CDMOs.
Key Duties and Responsibilities:
  • Provide technical leadership for drug substance manufacturing campaigns at external partners, serving as the senior technical decision-maker during active operations to ensure consistent, compliant, on-time execution and strong campaign readiness
  • Oversee triage, resolution, and documentation of execution-related deviations, ensuring rapid containment to protect product quality and supply
  • Lead cross-functional coordination across MSAT, Quality, and manufacturing teams, escalating and framing complex issues as needed
  • Own process operability and execution robustness at the manufacturing site, including batch record clarity and usability
  • Drive improvements in yield, cycle time, right-first-time performance, and overall manufacturing reliability
  • Lead campaign readiness, including implementation of CAPAs and process updates
  • Serve as the senior technical interface during manufacturing operations, providing day-to-day guidance and driving communication, responsiveness, and accountability at the site level during campaigns
  • Oversee real-time monitoring of batch and campaign performance, identifying risks, process drift, or execution gaps and drive timely technical interventions as needed to maintain schedule adherence, quality, and supply reliability
  • Escalate complex or non-routine issues requiring deeper process understanding to MSAT, ensuring clear technical framing and efficient handoff
  • Oversee implementation of approved process and operational changes, ensuring effective execution and expected performance outcomes
  • Build and strengthen Technical Services capability within biologics, including defining ways of working and developing technical staff
  • Drive a culture of accountability, urgency, and operational rigor

Knowledge and Skills:
  • Deep understanding of biologics drug substance manufacturing processes and cGMP operations
  • Strong experience with real-time manufacturing support, including batch execution, deviation management, and troubleshooting
  • Ability to identify and resolve technical issues quickly in a live manufacturing environment
  • Working knowledge of batch records, investigations, change control, and quality systems
  • Proven ability to operate effectively in a matrixed environment, coordinating across MSAT, Quality, and manufacturing teams
  • Strong communication skills with the ability to drive clear decisions under time-sensitive conditions
  • Demonstrated focus on execution, accountability, and operational rigor
  • Strong technical background in aseptic manufacturing operations.
  • Solid project management skills and experience managing complex projects.
  • Strong verbal and written communication skills: ability to expresses oneself clearly and concisely, by adjusting style, language and/or terminology as appropriate for the audience.
  • Strong leadership and an innate ability to collaborate and build relationships is critical.
  • Ability to work calmly and make sound decisions in a fast-moving environment of uncertainty and change
  • Flexibility to work shift hours required to cover critical process steps
  • Ability to travel, national and international, up to 30%

Education and Experience:
  • BS/BA degree in Biological Sciences, Chemical Engineering, Chemistry or related discipline; advanced degree preferred
  • Requires 10+ years of experience in biologics manufacturing, MSAT, or external manufacturing
  • Demonstrated experience supporting or leading manufacturing execution at a site or external partner
  • Experience with deviation management, investigations, and real-time technical troubleshooting in a cGMP environment
  • Prior experience working with external manufacturing partners strongly preferred
  • Previous leadership experience, including leading technical teams or cross-functional initiatives, preferred
  • Requires progressive experience in a management/leadership role in the biotechnology/ pharmaceutical industry with a focus on external manufacturing and commercial operations
  • Excellent communication and interpersonal skills, with the ability to influence cross-functional stakeholders and present insights to all levels of senior stakeholders
  • Demonstrated continuous improvement mindset, driving efficiencies, process improvements across diverse initiative

Pay Range:
$160,000 - $240,000
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
Hybrid-Eligible Or On-Site Eligible
Flex Eligibility Status:
In this Hybrid-Eligible role, you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Hybrid
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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