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Research And Development Project Manager information
See Florida salary details
$54.6K - $60.9K
11% of jobs
$60.9K - $67.3K
14% of jobs
$67.8K is the 25th percentile. Wages below this are outliers.
$67.3K - $73.7K
12% of jobs
$73.7K - $80.1K
13% of jobs
The median wage is $80.8K / yr.
$80.1K - $86.5K
15% of jobs
$90.5K is the 75th percentile. Wages above this are outliers.
$86.5K - $92.9K
19% of jobs
$92.9K - $99.3K
8% of jobs
$99.3K - $105.6K
5% of jobs
$105.6K - $112K
3% of jobs
$112K - $118.4K
0% of jobs
$118.4K - $124.8K
1% of jobs
$54.6K
$82.7K
$124.8K
How much do research and development project manager jobs pay per year?
What is the difference between Research And Development Project Manager vs Product Development Manager?
| Aspect | Research And Development Project Manager |
|---|
The Research And Development Project Manager focuses on overseeing R&D projects, managing innovation, and coordinating scientific or technical teams. They typically require technical credentials, such as engineering or science degrees, and work in labs or R&D departments. The Product Development Manager, on the other hand, concentrates on bringing products from concept to market, often requiring product management experience and market knowledge. Both roles are common in tech, manufacturing, and biotech industries, but their primary focus and skill sets differ. Understanding these distinctions helps in choosing the right career path or job search focus.
How does a Research and Development Project Manager typically collaborate with cross-functional teams during a project?
What does a Research and Development Project Manager do?
What are the key skills and qualifications needed to thrive as a Research and Development Project Manager, and why are they important?
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 17 days ago
ConMed rating
8.2
Based on 18 frontline employees who took The Breakroom Quiz
Job description
The R&D Project Manager will be responsible for overseeing and managing the development of new orthopedic products from concept to market launch. The ideal candidate will have a proven track record of successfully managing complex projects within the medical device or any other regulated industry, preferably with a PMP certification.
Key Responsibilities:
Project Planning and Scheduling: Develop and maintain detailed project plans, including timelines, milestones, and deliverables. Utilize project management software to track progress and ensure adherence to schedules.
Cost and Budget Management: Prepare and manage project budgets, ensuring projects are completed within financial constraints. Monitor expenditures and implement cost-saving measures as necessary.
Risk Management: Identify potential project risks and develop mitigation strategies. Conduct regular risk assessments and adjust plans as needed to address emerging issues.
Quality Management: Ensure compliance with regulatory requirements and industry standards throughout the product development process. Implement quality control measures to maintain high standards.
Stakeholder Management: Collaborate with R&D, Quality, Regulatory, Manufacturing, and Marketing teams to ensure alignment and successful project execution. Communicate project status and updates to senior management and stakeholders.
Resource Management: Allocate resources effectively to meet project objectives. Coordinate with team members and departments to ensure optimal resource utilization.
Performance Monitoring and Reporting: Conduct regular project status meetings and provide comprehensive updates to senior management. Utilize performance metrics to track project progress and identify areas for improvement.
Continuous Improvement: Drive continuous improvement initiatives within the project management process. Implement best practices and lessons learned from previous projects.
Team Leadership and Development: Mentor and guide junior project managers and team members. Foster a collaborative and innovative work environment.
Qualifications:
Bachelor’s degree in engineering
2 years of engineering experience with a focus on new product development, OR 3 years of PM experience preferably within the medical device industry.
Preferred Qualifications:
PMP ( Project Management Professional ) certification
Strong knowledge of design controls and regulatory requirements for medical devices.
Proven ability to manage multiple projects simultaneously and deliver results on time and within budget.
Excellent leadership, communication, and interpersonal skills.
Strong problem-solving and decision-making abilities.
Proficiency in project management software and tools (Smartsheet, MS Project, etc).
Expected Travel 0-20%
This position is not eligible for employer-visa sponsorship
This job posting is anticipated to close on July 6, 2026. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.
Benefits:
CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.
- Competitive compensation
- Excellent healthcare including medical, dental, vision and prescription coverage
- Short & long term disability plus life insurance -- cost paid fully by CONMED
- Retirement Savings Plan (401K) -- CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period
- Employee Stock Purchase Plan -- allows stock purchases at discounted price
- Tuition assistance for undergraduate and graduate level courses
Know someone at CONMED? Have them submit you as a referral before applying for this position to be eligible for our Employee Referral Program incentives!
CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. The Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.
Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-929-7176 option #5.