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Associate Director Clinical Trial Operations Jobs

RXinsider LTD.

Associate Director, Clinical Development & Operations Location: Columbus, OH Job Type: Full time ... Key clinical trial project tasks and milestones are completed on time. Each project stage and ...

Predicine, Inc

Clinical Trial Associate

Hayward, CA · On-site

$38.50 - $52.50/hr

The Clinical Trial Associate reports to Associate Director, Clinical Development and supports the planning, execution, and operational management of global clinical trials, working closely with ...

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How much do associate director clinical trial operations jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for associate director clinical trial operations in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does an associate director clinical trial operations do?

An Associate Director of Clinical Trial Operations oversees the planning, execution, and management of clinical trials within a pharmaceutical or biotechnology company. They are responsible for ensuring that clinical studies are conducted efficiently, in compliance with regulatory standards, and within budget and timeline constraints. This role involves leading cross-functional teams, managing vendor relationships, and collaborating with regulatory authorities. Additionally, they play a key role in developing and implementing clinical trial strategies to support the company's research and development goals.

What are the key skills and qualifications needed to thrive as an associate director clinical trial operations?

To thrive as an Associate Director Clinical Trial Operations, you need in-depth knowledge of clinical research, regulatory compliance, project management, and typically an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification are commonly required. Strong leadership, problem-solving, and excellent communication skills help drive teams and manage complex projects efficiently. These skills ensure clinical trials are conducted ethically, on time, and within budget, ultimately supporting successful drug development.

What are some common challenges faced by an associate director clinical trial operations, and how can they be addressed?

One common challenge in this role is balancing the need for timely trial execution with strict regulatory compliance and high-quality data standards. Associate Directors must coordinate across multiple teams, such as clinical research, data management, and regulatory affairs, often managing competing priorities and tight deadlines. Strong project management skills, proactive risk mitigation, and effective cross-functional communication are essential for overcoming these challenges. Regular training and staying updated on changing regulations also help ensure successful trial outcomes.

What cities are hiring for Associate Director Clinical Trial Operations jobs?

Cities with the most Associate Director Clinical Trial Operations job openings:

What states have the most Associate Director Clinical Trial Operations jobs?

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What are popular job titles related to Associate Director Clinical Trial Operations jobs?

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

Infographic showing various Associate Director Clinical Trial Operations job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Associate Director, Clinical Development Trial Lead (CDTL)

Stamford, CT • On-site

System One
Business Consulting Services • 5 - 10K employees
Learn more about System Oneexternal

$35.75 - $48.75/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Re-posted 23 days ago

Key responsibilities

  • Lead the development and execution of complex clinical trials, ensuring delivery of milestones on time, within scope, and within budget.

  • Coordinate with study teams, regional input, and cross-functional partners to support study design, conduct, and documentation.

  • Ensure trial documentation, including Trial Master File and deviations, is maintained in inspection-ready condition.

Job description

Job Title: Associate Director, Clinical Development Trial Lead Location: Stamford, CT Type: Contract - 1 year Work Model: Onsite – onsite Joulé is partnering with a leading pharmaceutical organization seeking an experienced Associate Director, Clinical Development Trial Lead to drive the execution of complex global oncology clinical trials. This highly visible leadership role offers the opportunity to oversee study strategy, enrollment, budgets, CRO partnerships, and cross-functional teams while influencing clinical development decisions on a global scale.

Responsibilities

  • Independently lead the cross-functional study team in the development and execution of complex clinical trials and ensure delivery of clinical milestones on trial(s) with quality, on time, and within scope and budget.
  • Demonstrate independent leadership and influence when working with study teams, management, and business partners, and proactively identify issues and resolve them.
  • Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process expertise to influence study design and program-level decisions considering regional needs.
  • Recognize inter-relatedness of cross-functional activities and understand the impact of project decisions on the overall clinical trial.
  • Coordinate and facilitate obtaining regional input to provide to the study teams.
  • Act as single point of accountability for the Trial Master File for assigned trials, working closely with functional record owners to ensure the file is current and inspection ready at all times.
  • Ensure inspection readiness of respective clinical trial(s), including timely documentation of deviations and creation of story boards or issue summary documents (e.g. for high-risk areas/hot topics).
  • Report, manage, and interpret information for the clinical trial(s), including completeness and accuracy across multiple business systems and tools.
  • Drive regional clinical operational processes and methodologies used.

Requirements

  • Bachelor's degree (scientific or health-related field preferred)
  • 5+ years clinical research experience or relevant experience in a scientific or health-related field
  • Minimum of 5 years clinical trial experience with a strong working knowledge of the clinical research process
  • Experience with oncology (early & late phase clinical trials)
  • Prior clinical trial site-level or affiliate experience
  • Prior experience with local/country regional requirements
  • Need to travel periodically to scientific/regional meetings

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M- #LI-MP1 Ref: #568-Clinical

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About System One

Sourced by ZipRecruiter

System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.

Industry

Business consulting services and recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Pittsburgh, PA, US

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