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Research Project 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 ... Project lead for other research staff assigned to multicenter studies. * Key decision maker for ...

ARTHREX

Sr. Clinical Study Manager

Naples, FL

Project lead for other research staff assigned to multicenter studies. * Key decision maker for ... Works closely with leadership, product management, medical writing, project manager, and other ...

LJA Engineering

Project Surveyor - Survey

Naples, FL · On-site

Responsible for supervision of field operations, technical and drafting staff, deed and map research, and project management. * Collaborate with architects, engineers, and project managers to ...

Zunch Staffing

Software Engineering Manager

Naples, FL

$185K - $250K/yr

Collaborate with cross-functional teams, including product management, design, and QA, to ensure seamless project execution. * Innovation and Research: Stay abreast of the latest trends in software ...

ARTHREX

Product Manager, Vet Systems

Naples, FL

Participates in overall product strategy, research and development requirements, development, and ... Directs and coordinates the activities of project team personnel (engineering, manufacturing ...

Arthrex

Product Manager, Vet Systems

Naples, FL · On-site

Participates in overall product strategy, research and development requirements, development, and ... Directs and coordinates the activities of project team personnel (engineering, manufacturing ...

ARTHREX

Product Manager, Hip Arthroscopy

Naples, FL

Participates in overall product strategy, research and development requirements, development, and ... Confers with project staff to outline/negotiate work plans, assign duties and responsibilities ...

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All JobsResearch Project JobsResearch Project Manager JobsResearch Project Manager Jobs in Naples, FL

Research Project Manager information

See Naples, FL salary details

$47.1K

$81K

$124.3K

How much do research project manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for research project manager in Naples, FL is $81,026.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,300.00 and $86,200.00 per year, depending on experience, location, and employer.

What does a research project manager do?

A Research Project Manager oversees the planning, execution, and completion of research projects within organizations such as universities, nonprofits, or private companies. Their responsibilities include coordinating teams, managing budgets and timelines, ensuring compliance with regulations, and communicating progress to stakeholders. They act as a bridge between researchers, administrative staff, and sometimes external partners, ensuring that project goals are met efficiently and effectively.

What are the key skills and qualifications needed to thrive as a research project manager?

To thrive as a Research Project Manager, you need expertise in project management, budgeting, and research methodologies, often supported by a relevant degree and experience in managing research teams or studies. Familiarity with project management software (like Asana or MS Project), data analysis tools (such as SPSS or R), and compliance certifications (like GCP) is typically required. Excellent organization, leadership, and communication skills help coordinate diverse teams and stakeholders effectively. These skills ensure that complex research projects are completed on time, within budget, and in accordance with regulatory and scientific standards.

What are some common challenges faced by research project managers when coordinating multidisciplinary teams?

Research Project Managers often coordinate teams comprising experts from various fields, which can present challenges related to communication, differing priorities, and aligning timelines. Successfully managing these dynamics requires strong interpersonal skills, clear communication, and the ability to mediate between stakeholders to ensure everyone is working toward shared project goals. Regular check-ins, transparent progress tracking, and fostering a collaborative team culture can help mitigate these challenges and keep projects on schedule.

What is the difference between Research Project Manager vs Research Coordinator?

AspectResearch Project ManagerResearch Coordinator
CredentialsBachelor's or Master's in relevant field; often requires project management certificationsBachelor's degree in related field; may require research experience
Work EnvironmentOversees multiple projects, manages teams, and coordinates with stakeholdersAssists with daily research activities, data collection, and participant coordination
Employer & Industry UsageResearch institutions, universities, healthcare, and biotech companiesAcademic research labs, clinical trials, healthcare organizations

The Research Project Manager typically handles project planning, team management, and stakeholder communication, while the Research Coordinator focuses on supporting research activities, data collection, and participant management. Both roles are essential in research settings but differ in scope and responsibilities.

What are popular job titles related to Research Project Manager jobs in Naples, FL?

For Research Project Manager jobs in Naples, FL, the most frequently searched job titles are:

What job categories do people searching Research Project Manager jobs in Naples, FL look for?

The top searched job categories for Research Project Manager jobs in Naples, FL are:

What cities near Naples, FL are hiring for Research Project Manager jobs?

Cities near Naples, FL with the most Research Project Manager job openings:

Research Project Manager jobs near you
Infographic showing various Research Project Manager job openings in Naples, FL as of June 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $81,026 per year, or $39 per hour.

Sr. Clinical Study Manager

Arthrex

Naples, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Arthrex rating

7.8

Company rating: 7.8 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

176th of 540 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: Jul 30, 2026
Requisition ID: 66722
Salary Range:
Job title: Sr. Clinical Study Manager
Research & Development
Location:

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