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Clinical Operations Associate Jobs in Florida (NOW HIRING)

The Associate Market Clinical Director will directly supervise, performance manage and train ... Ensures successful clinical operations and meeting/exceeding plan market earnings. * Manages ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

The Associate Center Clinical Director will directly supervise and train primary care providers ... Partnering with Center Operations Director/Market General Manager to drive continued improvement of ...

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Clinical Operations Associate information

See Florida salary details

$8

$19

$39

How much do clinical operations associate jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for clinical operations associate in Florida is $19.61, according to ZipRecruiter salary data. Most workers in this role earn between $13.27 and $22.64 per hour, depending on experience, location, and employer.

What is a Clinical Operations Associate job?

A Clinical Operations Associate supports the planning, execution, and management of clinical trials to ensure compliance with regulatory guidelines and company protocols. They assist in coordinating trial logistics, managing documentation, and communicating with study sites and stakeholders. Their role helps ensure studies run efficiently, meet regulatory requirements, and generate reliable data for drug development and approvals.

What do we mean by clinical?

In the context of a Clinical Operations Associate role, 'clinical' refers to activities related to the development, management, and oversight of clinical trials involving human participants. This includes tasks such as protocol adherence, data collection, and ensuring compliance with regulatory standards like GCP and FDA requirements.

What does very clinical mean?

In the context of a Clinical Operations Associate role, 'very clinical' typically refers to a work environment that is highly focused on medical, scientific, and regulatory aspects of clinical trials. It involves detailed knowledge of protocols, patient safety, and compliance with industry standards, often requiring familiarity with clinical software and certifications. This environment emphasizes precision, documentation, and adherence to strict procedures.

What are the key skills and qualifications needed to thrive in the Clinical Operations Associate position, and why are they important?

To thrive as a Clinical Operations Associate, you need a solid background in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) certification is highly valued. Attention to detail, strong organizational skills, and effective communication are important soft skills that help manage complex studies and collaborate with cross-functional teams. These abilities are crucial for ensuring that clinical trials run smoothly, meet regulatory standards, and maintain participant safety.

What are the typical responsibilities and team dynamics for a Clinical Operations Associate?

As a Clinical Operations Associate, your typical responsibilities include coordinating study activities, maintaining trial documentation, supporting regulatory submissions, and ensuring adherence to protocols and timelines. You will often work as part of a multi-disciplinary team that includes clinical research coordinators, data managers, and study monitors, frequently communicating with internal and external stakeholders to keep the study on track. Collaboration and adaptability are key, as priorities can shift based on site needs or regulatory updates. This role offers valuable exposure to the operations side of clinical research and can serve as a springboard to more senior roles such as Clinical Project Manager or Clinical Research Associate.

What does it mean for someone to be clinical?

In the context of a Clinical Operations Associate, being clinical refers to working within healthcare or medical research environments, often involving tasks related to patient interactions, clinical trials, or medical data management. It requires understanding clinical protocols, regulatory requirements, and often involves collaboration with healthcare professionals and adherence to safety standards.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If referring to a film with that name, it typically involves themes related to medical or psychological clinical settings. For job roles like Clinical Operations Associate, understanding medical or clinical environments can be relevant, but the question appears unrelated to the job itself.
What are the most commonly searched types of Clinical Operations jobs in Florida? The most popular types of Clinical Operations jobs in Florida are:
What cities in Florida are hiring for Clinical Operations Associate jobs? Cities in Florida with the most Clinical Operations Associate job openings:

Associate Director, Clinical Data Management & Systems | Jacksonville, FL

Johnson & Johnson

Jacksonville, FL • On-site

Full-time

Medical, Vision, Life

Posted 13 days ago


Johnson & Johnson rating

8.1

Company rating: 8.1 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

31st of 71 rated pharmaceutical


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.

Job Function:

Data Analytics & Computational Sciences

Job Sub Function:

Clinical Data Management

Job Category:

Professional

All Job Posting Locations:

Jacksonville, Florida, United States of America

Job Description:

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.

Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that's reimagining how vision is improved? 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 Data Management & Systems to join our J&J Vision team. This position is based in Jacksonville, FL. Other J&J Vision locations may be considered for the ideal candidate.

Purpose:

As a member of the Statistics and Clinical Data Management Leadership Team, the Associate Director, Clinical Data Management & Systems will lead data management and system support across the J&J Vision portfolio, ensuring reliable, compliant, and high-quality clinical trial data. This role sets strategy for data standards, databases, systems, vendor oversight, and timely delivery of clean data to support study execution, analysis, and regulatory submissions. The Associate Director will work closely with the Global Head of Statistics and Clinical Data Management to ensure alignment in strategy, resource planning and excellence in execution. Collaboration with the departments of Statistics, Clinical Operations, Clinical Science, Regulatory Affairs, and external partners is crucial to strengthen operational excellence, inspection readiness, and continuous improvement across the Surgical Vision and Vision Care businesses, an outstanding opportunity to shape critical work across the portfolio.

You will be responsible for:

  • Provide strategic leadership for Clinical Data Management across the medical devices portfolio in support of Johnson & Johnson Vision's clinical, regulatory, and business priorities.
  • Oversee planning, execution, and delivery of core data management activities, including database build, edit checks, data review, coding, reconciliation, and database locks.
  • Establish and maintain standards, processes, and system workflows that enable efficient, consistent, and compliant study execution.
  • Act as the subject matter expert for clinical data management systems supporting Clinical Operations (e.g. CTMS) and Clinical Science (e.g. SDTM) and processes, advising on data quality, system capabilities, and operational best practices.
  • Drive data quality and integrity through proactive review, issue management, metrics, and risk-based methods that support timely clinical decisions.
  • Lead oversight of external vendors and technology partners to ensure strong service, on-time delivery, and compliance with study and regulatory requirements.
  • Collaborate with Clinical Operations, Clinical Science, Statistics, Statistical Programming, Medical Safety, and Regulatory Affairs to support startup, study conduct, analysis, and submission readiness.
  • Support audits and regulatory inspections by maintaining inspection-ready documentation, compliant processes, and effective responses to data management questions and audit findings.
  • Build and develop internal and external Clinical Data Management team members through clear goals, coaching, training, and performance support.
  • Advance continuous improvement and harmonization of data management processes, systems, and standards to increase efficiency and support evolving business needs.
  • Ensure all activities are performed in accordance with applicable regulations, GCP, company policies, and quality expectations.

Qualifications:

  • Bachelor's degree required; an advanced degree in life sciences, health sciences, data management, information systems, or a related field is strongly preferred.
  • Minimum of 8 years relevant Clinical Data Management experience in clinical research (pharmaceutical, biotechnology, or medical devices / diagnostics industry) is required.
  • People and/or functional leadership experience, including management of a team is required.
  • Demonstrated leadership of clinical data management activities across multiple clinical studies, including database setup, edit checks, data review, coding, reconciliation, and database lock is required.
  • Hands-on experience with electronic data capture, clinical systems, and related technologies; familiarity with at least one EDC system is essential.
  • Strong knowledge of CDISC data standards (SDTM & ADaM) is required; experience with data integrations, and process automation is preferred.
  • Solid understanding of GCP, and applicable global regulations (e.g. ISO 14155, 21 CFR Part 11) is required.
  • Experience overseeing external vendors, managing contractors and collaborating effectively with cross-functional stakeholders is strongly preferred.
  • Exposure supporting audits, inspections, and regulatory submissions.
  • Excellent oral and written communication, organization, and problem-solving skills.
  • Position is based in Jacksonville, Florida, though other J&J Vision locations may be considered for the ideal candidate. Fully remote work is not available.
  • Ability to travel domestically up to 25% may be needed.

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.

#LI-JS3

#LI-hybrid

Required Skills:

Clinical Data Management, Clinical Research, GCP Auditing, Leadership

Preferred Skills:


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