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Associate Director Clinical Operations Jobs in Texas

The Director Clinical Operations position will work in conjunction with Physician Organization (PO ... Represents clinical practices in health care programs and professional organizations of associates ...

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Associate Director Clinical Operations information

See Texas salary details

$55.9K

$136K

$263.2K

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

As of Sep 12, 2026, the average yearly pay for associate director clinical operations in Texas is $135,993.00, according to ZipRecruiter salary data. Most workers in this role earn between $95,000.00 and $161,600.00 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 Texas?

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

What cities in Texas are hiring for Associate Director Clinical Operations jobs?

Cities in Texas with the most Associate Director Clinical Operations job openings:

Infographic showing various Associate Director Clinical Operations job openings in Texas as of September 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $135,993 per year, or $65.4 per hour.

Associate Director, Clinical Operations | Jacksonville, FL

Jacksonville, TX • On-site

Other

Medical, Vision, Life

Posted 6 days ago


Job description

Job Function:

R&D Operations

Job Sub Function:

Clinical Trial Project Management

Job Category:

Professional

All Job Posting Locations:

Jacksonville, Florida, United States of America

Job Description:

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

About Vision

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.

Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent for an Associate Director, Clinical Operations to join our J&J Vision team. This position is based in Jacksonville, FL.

Purpose:

The Associate Director, Clinical Operations develops strategies to address complex clinical issues. The Associate Director manages the strategic elements of study conduct, ensuring that operating procedures and company policies are followed. The Associate Director develops and manages timelines, resources, and budgets for JJV clinical trials worldwide. As a spokesperson and technical expert for Clinical Operations, the Associate Director provides compelling rationales for decisions and communicates complex strategies clearly.

Leads innovation and establishes operating practices across the functional area while fostering cross-functional collaboration and effective team performance. Manages multiple clinical studies across product platforms and directs and mentors study managers to ensure delivery of project objectives. Builds and manages relationships with external strategic partners and ensures compliance with policies, procedures, and departmental objectives.

You will be responsible for:
  • Own the processes and information required to execute and support clinical trials, including the clinical trial project plan, project timelines, resource plans, budget plans, clinical study agreements, and statements of work (30%).
  • Be accountable for the preparation and finalization of key clinical documents, including the clinical protocol, informed consent forms, case report forms, training materials, and other essential study documents (20%).
  • Manage study conduct, ensuring that operating procedures and company policies are followed and that trials meet all applicable regulations and guidelines required to gain approval for testing investigational ophthalmic devices (25%).
  • Lead the selection of contract research organizations (CROs) and oversee contracts, timelines, and budgets, when applicable (10%).
  • Manage and improve clinical trial processes, including benchmarking and leveraging across other J&J companies (10%).
  • Perform other related duties as assigned by management (5%).
QualificationsRequired:
  • Minimum of a bachelor’s degree.
  • Minimum of 8 years’ experience in clinical research in a medical device or pharmaceutical regulated industry.
  • Understanding and application of clinical research principles, concepts, procedures, and Good Clinical Practice (GCP).
  • Strong communication, organizational and interpersonal skills.
  • Ability to negotiate effectively and influence peers, affiliates, and regulatory agencies to ensure that regulatory and business needs are met.
  • Ability to work hybrid out of the Jacksonville, FL office location.
  • Up to 10% business travel may be required.
Preferred:
  • Master’s or PhD degree in a scientific discipline.
  • Minimum of 2 years’ experience as a clinical research associate.
  • People management experience.
  • Broad understanding of ophthalmology and medical devices or instrumentation used in ophthalmic surgery.
  • Broad-based technical knowledge and skills across diverse business areas (e.g., Operations, Quality Assurance, laboratory, Regulatory, and project management).
  • Strategic and tactical clinical and business knowledge to support product approvals and maintenance of legal marketing status.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please contact us via https://www.jnj.com/contact-us/careers or contact AskGS to be directed to your accommodation resource.

Required Skills:

Clinical Research, Communication

Preferred Skills:

Good Clinical Practice (GCP), Ophthalmology, People Management

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