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Data Processing Manager Jobs in Naples, FL (NOW HIRING)

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

Manages site initiation activities (e.g., study start-up documentation preparation) * Responsible ... data collection and analytical processes are required. * The ability to identify a research ...

RxSight, Inc.

Account Manager (Southeast)

Naples, FL

$130K/yr

... processes that support same-store-sales growth as a core team function. AMs gather customer data to ... Develop and manage site-level account plans aligned to the area's strategic priorities and to ...

RXSIGHT INC

Account Manager (Southeast)

Naples, FL · On-site

... processes that support same-store-sales growth as a core team function. AMs gather customer data to ... Develop and manage site-level account plans aligned to the area's strategic priorities and to ...

RxSight

Account Manager (Southeast)

Naples, FL · On-site

$130K/yr

... processes that support same-store-sales growth as a core team function. AMs gather customer data to ... Develop and manage site-level account plans aligned to the area's strategic priorities and to ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

Monitor the management of and collection of data. * Ensures compliance with the Clinical Trial ... Lead clinical trial agreement negotiations to ensure efficient and timely processing of clinical ...

ARTHREX

Clinical Study Manager

Naples, FL · On-site

Monitor the management of and collection of data. * Ensures compliance with the Clinical Trial ... Lead clinical trial agreement negotiations to ensure efficient and timely processing of clinical ...

Rentvine

Onboarding Project Manager

Estero, FL · On-site

You'll get into the data - building migration files, checking balances - working alongside our ... Push what you learn back into the process, so we're not solving the same problem from scratch on ...

Fifth Third

Senior Wealth Strategy Analyst

Naples, FL · On-site

$80K - $100K/yr

Data Review & Organization: Review and organize client financial information, including personal ... Process Management & Execution: Track deliverables, identify missing or incomplete information, and ...

ReachMobi

Product Manager - HYBRID

Bonita Springs, FL · On-site

Our ethos is simple: have an idea in the morning, ship it by the afternoon, and have data by the ... We focus on action over process and don't get stuck in unnecessary meetings or red tape. Everyone ...

ReachMobi

Product Manager - HYBRID

Bonita Springs, FL · On-site +1

Our ethos is simple: have an idea in the morning, ship it by the afternoon, and have data by the ... We focus on action over process and don't get stuck in unnecessary meetings or red tape. Everyone ...

ReachMobi

Product Manager - HYBRID

Bonita Springs, FL · On-site

Our ethos is simple: have an idea in the morning, ship it by the afternoon, and have data by the ... We focus on action over process and don't get stuck in unnecessary meetings or red tape. Everyone ...

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Showing results 21-40

All JobsData Processing JobsData Processing Manager JobsData Processing Manager Jobs in Naples, FL

Data Processing Manager information

See Naples, FL salary details

$32.5K

$49.4K

$64.5K

How much do data processing manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for data processing manager in Naples, FL is $49,445.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,000.00 and $58,900.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a data processing manager?

To thrive as a Data Processing Manager, you need expertise in data management, analysis, and process optimization, typically supported by a degree in computer science, information systems, or a related field. Familiarity with database management systems (DBMS), ETL tools, and data governance frameworks, along with certifications like Certified Data Management Professional (CDMP), is often required. Strong leadership, problem-solving, and communication skills help you effectively lead teams and collaborate across departments. These skills are crucial for ensuring data integrity, efficient workflows, and informed decision-making within an organization.

What are the typical challenges faced by a data processing manager when overseeing large-scale data projects?

Data Processing Managers often encounter challenges such as ensuring data quality and consistency across multiple sources, managing tight project deadlines, and coordinating with cross-functional teams like IT, analytics, and compliance. They must stay updated on evolving data processing technologies while maintaining security and privacy standards. Effective communication and adaptability are essential, as priorities may shift quickly based on organizational needs or data integrity issues.

What does a data processing manager do?

A data processing manager oversees the collection, organization, and analysis of data within an organization. They coordinate data workflows, ensure data quality, and implement processing systems using tools like SQL, Python, or data management software. Strong leadership, technical skills, and understanding of data security are essential for this role.

What are popular job titles related to Data Processing Manager jobs in Naples, FL?

For Data Processing Manager jobs in Naples, FL, the most frequently searched job titles are:

What job categories do people searching Data Processing Manager jobs in Naples, FL look for?

The top searched job categories for Data Processing Manager jobs in Naples, FL are:

What cities near Naples, FL are hiring for Data Processing Manager jobs?

Cities near Naples, FL with the most Data Processing Manager job openings:

Data Processing Manager jobs near you
Infographic showing various Data Processing Manager job openings in Naples, FL as of August 2026, with employment types broken down into 84% Full Time, 15% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $49,445 per year, or $23.8 per hour.

Sr. Clinical Study Manager

Arthrex

Naples, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Arthrex rating

7.8

Company rating: 7.8 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

169th of 545 rated manufacturers

Job description

Requisition ID: 66722 Title:Sr. Clinical Study Manager
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Sr. Clinical Study Manager. This individual will be responsible for leading, developing, managing, and facilitating activities related to the conduct of clinical research studies. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.
This is an onsite position based at our global headquarters in Naples, Florida.
Essential Duties and Responsibilities:
  • Leading, planning, executing, managing, and oversight of clinical studies according to research ethics guidelines, ISO standards, internal SOPs, applicable regulations, and portfolio priorities.
  • Leads the implementation of clinical protocols, informed consent forms, and study-related materials for clinical studies.
  • Manages site initiation activities (e.g., study start-up documentation preparation)
  • Responsible for IRB communication, including document preparation and submission of Arthrex study initiatives.
  • Implementing modifications to optimize protocol results or edit/amend study documentation if necessary.
  • Collaborate with Data Management team to ensure the electronic data capture system (EDC) is designed to collect all required data per the protocol.
  • Responsible for training internal staff assigned to studies.
  • Project lead for other research staff assigned to multicenter studies.
  • Key decision maker for study amendments and strategies
  • Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies.
  • Oversee all aspects of the assigned clinical projects, including essential documents, electronic data collection, change management, risk management, and monitoring activities.
  • Set-up and maintain accurate progress and Site study status tracking logs to provide reports and updates of assigned clinical research projects.
  • Oversee follow-up and lead query resolution with sites via ongoing interactions.
  • Participation in investigator meetings, Site initiation, monitoring, and close-out visits when applicable
  • Complete central, remote, and on-site monitoring reports and follow-up letters
  • Complete monitoring report reviews of other staff
  • Oversee monitoring activities for the assigned projects and is responsible for ensuring actions are taken when applicable.
  • Identify and mitigate quality risk and/or issues associated with assigned studies/activities.
  • Facilitate appropriate documentation to maintain compliance with the Finance and Compliance departments.
  • Prepare and track clinical study budgets that include both sponsor costs and sites costs.
  • Responsible for the timely completion of deliverables, inclusive of contributing to interim and final study reports
  • Facilitate efficient utilization of available clinical data, addressing the needs of internal and external stakeholders (e.g., publications)
  • Works closely with leadership, product management, medical writing, project manager, and other research staff to manage assigned studies.
  • Conducts regular investigator meetings to ensure protocol compliance and site engagement.
  • Actively participate in research committees, study groups, and cross-functional portfolio governance activities to support continuous improvement and strategic alignment
  • Engage in and support departmental initiatives and cross-functional team projects, collaborating by driving execution, problem-solving, and achievement of key business outcomes.
  • Conducts project huddles and able to lead cross-functional projects.
  • Mentoring and training staff
  • Serve as a cross-functional lead within an assigned study and product portfolio, ensuring alignment across Clinical Operations, Product Management, Data Management, Regulatory, Compliance, and other key stakeholders

Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • Strong strategic thinking with the ability to translate goals into actionable project plans.
  • An understanding of cross-functional clinical study processes is required.
  • Ability to work in a team, good communication, documentation, and a strong understanding of data collection and analytical processes are required.
  • The ability to identify a research hypothesis and proposed outcome measures to address the hypothesis is required.
  • The ability to read a surgical technique and have a basic understanding of the instruments necessary to perform the procedure is required.
  • Able to communicate effectively with physicians, key opinion leaders, and other healthcare personnel.
  • Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics.
  • Experience in managing research contracts and protocol development is preferred.
  • Experience in post-market, real world evidence, longitudinal or health economics studies is preferred.
  • Ability to generate and develop ideas that drive efficiency and impact organizational goals.
  • Ability to approach challenges with an innovative, solution-oriented mindset.

Education and Experience:
  • Bachelor's degree required. Master's degree preferred.
  • 6 plus years of related clinical research experience required.
  • Three-year Sponsor/CRO preferred. Preferably, in a medical device industry environment
  • One year of clinical research monitoring or study manager experience required.
  • Familiarity with orthopedics and medical terminology is preferred.
  • Strong research and technical writing skills and ability to review protocols and agreements for accuracy.
  • Ability to organize and review data sets
  • Proficiency in Microsoft Office programs
  • Clinical Research Certification required or must be willing to obtain within 1 year of employment.

Arthrex Benefits
  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.
Making People Better at Arthrex
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Job Details
Date: Aug 28, 2026
Requisition ID: 66722
Salary Range:
Job title: Sr. Clinical Study Manager
Research & Development
Location:

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