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Associate Director Clinical Operations Jobs in Austin, TX

Role Description We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role ...

Role Description We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role ...

Role Description We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role ...

Role Description We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role ...

The VP will partner closely with Medical Directors, Product, Technology, Data Science, and Client Success teams to support program implementation, clinical workflow optimization, and operational ...

The Director of Clinical Data & AI is the global functional leader responsible for the strategy, architecture, and operational execution of clinical data and AI capabilities supporting end-to-end ...

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Associate Director Clinical Operations information

See Austin, TX salary details

$59.5K

$144.7K

$280K

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

As of Aug 27, 2026, the average yearly pay for associate director clinical operations in Austin, TX is $144,686.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,100.00 and $172,000.00 per year, depending on experience, location, and employer.

What does an associate director 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.

How does an associate director 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 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 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 popular job titles related to Associate Director Clinical Operations jobs in Austin, TX?

For Associate Director Clinical Operations jobs in Austin, TX, the most frequently searched job titles are:

What job categories do people searching Associate Director Clinical Operations jobs in Austin, TX look for?

The top searched job categories for Associate Director Clinical Operations jobs in Austin, TX are:

What cities near Austin, TX are hiring for Associate Director Clinical Operations jobs?

Cities near Austin, TX with the most Associate Director Clinical Operations job openings:

Infographic showing various Associate Director Clinical Operations job openings in Austin, TX as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 11% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $144,686 per year, or $69.6 per hour.

Director of Clinical Operations

Austin, TX • On-site

Senseye
Scientific Research and Development Services • 11 - 50 employees

$18K - $205K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Job description

About Us

Senseye is a NeuroTechnology Company in Austin, TX on the cusp of revolutionizing Mental Health. Over the past 6 years we have invested millions of dollars in R&D to build our platform allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases we are now focused on building the world's first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform, that gives clinicians a safe and objective accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for hundreds of millions of sufferers. The Senseye platform has the potential to be the technology that drives this change.

Role Description

We are seeking a Director of Clinical Operations to lead the execution of clinical programs supporting product validation, regulatory submissions, and commercialization. This role combines strategic oversight with hands-on execution and includes direct management of clinical operations personnel and external partners. You will play a key role in building and scaling our clinical capabilities as the company grows.

Responsibilities
  • Lead and execute clinical studies from early validation through pivotal trials
  • Oversee and mentor clinical operations team members, fostering strong execution and professional development
  • Manage and coordinate external partners, including CROs, sites, and investigators
  • Design study protocols and generate evidence to support regulatory and commercial goals
  • Collaborate cross-functionally with Research, Artificial Intelligence, and Regulatory teams
  • Support FDA submissions and clinical documentation
  • Contribute to scientific publications and presentations
  • Ensure compliance with GCP and applicable regulations

Requirements

  • Bachelor’s degree in a relevant field (Master’s or PhD preferred)
  • 5–8+ years of experience in clinical research, clinical operations, or clinical affairs
  • Demonstrated experience leading or managing clinical teams or vendors (e.g., CROs)
  • Experience in medtech, digital health, or neurotechnology
  • Familiarity with FDA clinical/regulatory pathways
  • Strong cross-functional collaboration and communication skills
Nice to Have
  • Experience in mental health or neuroscience
  • Background in digital biomarkers or AI-driven diagnostics
  • Startup or high-growth company experience
  • Experience building or scaling clinical operations functions

Benefits

  • The freedom and trust to define your role as we design, build, and ship our products
  • Competitive salary and stock option plan
  • Flexible paid time off (vacation, sick leave, and public holidays)
  • Flexible schedules
  • Company health care plan
    • Medical, dental, and vision insurance
    • Short and long term disability insurance
    • Life insurance policy
  • 401k
  • Commuter benefits for parking, public transit, carshares, etc.
  • Mothers' room
  • Fully stocked kitchen
  • Opportunities for continuing education

The compensation for this role is $180,00 - $205000 annually.

Senseye is dedicated to building a community of employees that are diverse, passionate, and engaged. We are committed to equal opportunity regardless of race, color, ancestry, religion, gender, gender identity, parental or pregnancy status, national origin, sexual orientation, age, marital status, disability, or veteran status. When we're safe, healthy, and balanced we can accomplish phenomenal things together.


Senseye logo

About Senseye

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

11 - 50 Employees

Headquarters location

Austin, TX, US

Year founded

2015

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