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Associate Director Of Clinical Operations Jobs in Florida

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Associate Director Of Clinical Operations information

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$44.8K

$109.1K

$211.1K

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

As of Aug 25, 2026, the average yearly pay for associate director of clinical operations in Florida is $109,082.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,200.00 and $129,700.00 per year, depending on experience, location, and employer.

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 healthcare or pharmaceutical organization. They ensure that studies comply with regulatory requirements, company standards, and timelines. Their responsibilities often include managing clinical teams, collaborating with cross-functional departments, and overseeing budgets and resources. This role is pivotal in driving clinical programs from start to finish, ensuring quality and efficiency in all operations.

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

To excel as an Associate Director of Clinical Operations, you need a solid background in clinical research, regulatory compliance, and project management, typically supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and industry certifications such as PMP or CCRP is highly beneficial. Outstanding leadership, strategic thinking, and effective communication skills set top performers apart in this role. These competencies ensure efficient study execution, regulatory adherence, and team coordination, which are critical for successful clinical trial outcomes.

What are some common challenges faced by an associate director of clinical operations, and how can they be effectively managed?

Associate Directors of Clinical Operations often encounter challenges such as coordinating cross-functional teams, ensuring regulatory compliance, and managing tight project timelines. Balancing the needs of different stakeholders—including clinical staff, regulatory bodies, and sponsors—requires strong communication and organizational skills. Proactively addressing potential bottlenecks, maintaining open lines of communication, and fostering collaborative relationships across departments are key strategies for overcoming these challenges. Additionally, staying updated on industry regulations and best practices helps ensure smooth clinical trial execution and successful project outcomes.

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

AspectAssociate Director Of Clinical OperationsClinical Project Manager
ResponsibilitiesOversees multiple clinical projects, manages teams, and develops operational strategiesManages individual clinical trials, coordinates project activities, and ensures timelines
Required CredentialsBachelor's or higher in life sciences, with experience in clinical operationsBachelor's in life sciences or related field, with project management experience
Work EnvironmentCorporate clinical operations departments, often in biotech or pharma companiesClinical trial sites, CROs, or pharmaceutical companies

The Associate Director Of Clinical Operations typically oversees multiple projects and manages teams, focusing on strategic operational functions. In contrast, a Clinical Project Manager handles specific clinical trials, focusing on day-to-day project execution. Both roles require relevant scientific credentials and experience in clinical settings, but their scope and responsibilities differ significantly.

What are the most commonly searched types of Director Of Clinical Operations jobs in Florida?

The most popular types of Director Of Clinical Operations jobs in Florida are:

What are popular job titles related to Associate Director Of Clinical Operations jobs in Florida?

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

What job categories do people searching Associate Director Of Clinical Operations jobs in Florida look for?

The top searched job categories for Associate Director Of Clinical Operations jobs in Florida are:

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

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

Infographic showing various Associate Director Of Clinical Operations job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $109,082 per year, or $52.4 per hour.

Director of Clinical Operations

Miami, FL • On-site

Other

Posted 14 days ago


Job description

Our client is seeking a Director/Manager of Clinical Operations, Phase I, to oversee clinical trials, ensure protocol adherence, and manage staff and operational aspects of studies. Requires strict compliance with GCP, ICH guidelines and company SOPs, with core duties spanning staff management, protocol review, quality assurance and study supervision.


Responsibilities

  • Lead and mentor the clinical operations team, fostering a collaborative and efficient environment
  • Ensure protocol compliance and maintain high quality standards across studies
  • Partner with Principal Investigators and the Site Director to assign studies and develop enrollment strategies
  • Oversee HR functions including staff evaluations, recruitment and training
  • Monitor protocol adherence and report deviations to sponsors and regulatory bodies
  • Coordinate with the Site Director and Principal Investigators to assign clinical research coordinators
  • Review study components with PIs and Site Directors ahead of study initiation
  • Conduct study closeout procedures
  • Ensure compliance with FDA, ICH and GCP regulations


Minimum qualifications

  • Bachelor's degree in a scientific or healthcare related field
  • Phase I or early phase experience
  • 7-10 years of clinical operations experience, including 5+ years in a senior leadership role
  • Strong understanding of FDA, ICH and GCP regulations and guidelines
  • Strong communication, organisational and leadership skills
  • Proficiency in Microsoft Word, Excel and clinical trial management software
  • In-depth knowledge of clinical trial operations, including study start-up, site selection, patient recruitment, monitoring, data management and study close-out
  • Experience managing and mentoring a team of clinical operations professionals
  • Bilingual in English and Spanish