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Medtech Project Manager Jobs in Edison, NJ (NOW HIRING)

Capabilities Associate Director

Raritan, NJ ยท On-site

$130 - $180/hr

Project Management * Data Analysis * Compliance Support Hard Skills * HEMA Competency Framework ... MedTech * HEMA * Evidence Generation * Market Access * Adoption * Growth Tools & Technologies

New

Sr Mgr EHS

New Brunswick, NJ ยท On-site

$85K - $116K/yr

... for a Sr Manager EHS in New Brunswick, NJ, with consideration given at the discretion of the ... projects. Leads the deployment of the J&J MedTech EHS&S External Supply program. Drives supplier ...

... for a Sr Manager EHS in New Brunswick, NJ, with consideration given at the discretion of the ... projects. Leads the deployment of the J&J MedTech EHS&S External Supply program. Drives supplier ...

... for a Sr Manager EHS in New Brunswick, NJ, with consideration given at the discretion of the ... projects. Leads the deployment of the J&J MedTech EHS&S External Supply program. Drives supplier ...

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Project/Program Management Group Job Sub Function: Project/Program Management Job Category:

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Project leadership and problem solving * Ability to convey value proposition to all levels of key ...

Manager, MT Group Finance - LRFP

New Brunswick, NJ ยท On-site +1

$112K - $153K/yr

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate ... Lead and contribute to high-impact strategic projects, executive analyses, and special requests.

Showing results 41-60

Medtech Project Manager information

See Edison, NJ salary details

$39.9K

$106.3K

$167.7K

How much do medtech project manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for medtech project manager in Edison, NJ is $106,302.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,300.00 and $127,300.00 per year, depending on experience, location, and employer.

What does a Medtech project manager do?

A Medtech Project Manager oversees the planning, execution, and delivery of projects related to medical technology, such as the development of medical devices or healthcare software. They coordinate cross-functional teams, manage timelines and budgets, and ensure compliance with regulatory standards. Their role is crucial in bridging the gap between technical development, clinical requirements, and business goals to bring innovative medical solutions to market efficiently and safely.

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

To thrive as a Medtech Project Manager, you need a strong background in project management, biomedical engineering or life sciences, and a solid understanding of regulatory requirements, often supported by a relevant degree and PMP or similar certification. Familiarity with project management software like MS Project or Jira, as well as knowledge of FDA/CE regulations and quality management systems, is typically required. Exceptional leadership, communication, and problem-solving skills help drive cross-functional teams and manage stakeholder expectations. These abilities ensure timely product development, regulatory compliance, and successful project outcomes in the highly regulated Medtech industry.

How does a Medtech project manager typically collaborate with cross-functional teams during the product development lifecycle?

A Medtech Project Manager frequently works with cross-functional teams, including R&D, regulatory affairs, quality assurance, marketing, and manufacturing. They coordinate efforts by facilitating regular meetings, setting clear timelines, and ensuring all team members are aligned with project goals and compliance requirements. Strong communication skills are essential, as the Project Manager must translate technical updates between departments and resolve potential roadblocks promptly. This collaborative approach helps deliver innovative medical technologies efficiently while meeting regulatory standards.

What is the difference between Medtech Project Manager vs Medical Device Engineer?

AspectMedtech Project ManagerMedical Device Engineer
Required credentialsBachelor's in engineering, project management certification (PMP)Bachelor's or higher in biomedical, mechanical, or electrical engineering
Work environmentProject teams, cross-functional collaboration, client interactionsDesign, development, testing, and manufacturing of medical devices
Employer & industry usageMedical device companies, healthcare tech firmsMedical device manufacturing, R&D departments
Common search & comparison intentUnderstanding project management roles in medtechTechnical engineering roles in medical device development

The Medtech Project Manager focuses on overseeing medical device projects, coordinating teams, and ensuring timely delivery. In contrast, a Medical Device Engineer is primarily involved in designing, developing, and testing medical devices. Both roles require engineering backgrounds, but their daily tasks and responsibilities differ significantly, catering to different aspects of the medical device lifecycle.

What are popular job titles related to Medtech Project Manager jobs in Edison, NJ?

For Medtech Project Manager jobs in Edison, NJ, the most frequently searched job titles are:

What cities near Edison, NJ are hiring for Medtech Project Manager jobs?

Cities near Edison, NJ with the most Medtech Project Manager job openings:

Infographic showing various Medtech Project Manager job openings in Edison, NJ as of June 2026, with employment types broken down into 90% Full Time, 7% Part Time, 1% Temporary, and 2% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $106,302 per year, or $51.1 per hour.

Solution Sales Specialist - Study Experience (CTMS / MedTech)

Medidata Solutions

New York, NY โ€ข On-site

$135K - $160K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 12 days ago


Job description

Location: This is a remote position
Medidata follows a hybrid office policy in which employees who are hired for an in-person position are expected to work on site a certain number of days per week following Company policy.
About our Company:
Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systรจmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com . Listen to our latest podcast, from Dreamers to Disruptors , and follow us at @Medidata.
About the Team:
Medidata is looking for a Clinical Operations Subject Matter Expert (SME) and Sales Specialist to lead expansion for our Study Experience solutions within a defined MedTech territory.
This is not a generalist software sales role. We are looking for a commercial SME with deep domain expertise and a track record selling Clinical Operations cloud platforms - CTMS, eTMF, and Site Payments - to MedTech companies. You will be the definitive commercial expert. Your role is to increase adoption of our Study Experience portfolio. This portfolio unifies design, planning, build, execution, finance, and closeout of clinical trials within a single, connected environment.
Responsibilities:
Commercial & Domain Subject Matter Expertise
  • Be the primary commercial SME for Medidata's Study Experience portfolio across the MedTech territory, bringing deep, hands-on understanding of Clinical Operations workflows, CTMS, eTMF, and Site Payments.
  • Collaborate with Product, Marketing, and Strategy teams to channel market intelligence, competitive insights, and customer feedback directly into product roadmaps.
  • Build relationships with customers to understand their challenges, priorities, and projects, translating them into compelling solution recommendations.
  • Navigate a collaborative, cross-functional sales environment.
Sales Execution & Territory Growth
  • Achieve or exceed quarterly and annual sales targets by increasing new business opportunities and securing renewals within the assigned territory.
  • Partner with Account/Territory Managers throughout the sales cycle to prospect opportunities, qualify customer needs, develop account strategies, and accelerate high-value negotiations requiring deep Clinical Operations platform knowledge.
  • Lead end-to-end value selling efforts, presenting tailored business cases, ROI models, and solution demonstrations to C-suite and VP-level Clinical Operations partners.
  • Maintain accurate pipeline, forecasting, and opportunity information within company systems as directed, including Salesforce.com
Qualifications:
  • Deep Domain Expertise requires demonstrated hands-on experience selling or supporting Clinical Operations cloud platforms. This experience must include explicit expertise in CTMS (Clinical Trial Management Systems), eTMF (electronic Trial Master File), and/or Site Payment solutions.
  • Sales Track Record: experience selling to clinical-stage companies, with a record of exceeding sales quotas.
  • Deal Complexity: Experience negotiating complex software (AI enabled or native platforms) and professional services contracts.
  • Experience establishing communication and engagement with prospects, with the ability to engage, communicate value, and build trust with C-suite level executives. Forecasting, pipeline management, territory planning, and account management skills.
  • Education: Bachelor's degree in Life Sciences, Computer Science, Engineering, or equivalent professional experience.
  • Ability to travel approximately 30-50%, depending on needs.
The salary range posted below refers only to positions that will be physically based in New York City. As with all roles, Medidata sets ranges based on several factors including function, level, candidate expertise, and geographic location. Pay ranges for candidates in locations other than New York City, may differ based on the local market data in that region. The base salary pay range for this position is $135,000-$160,500.
Base pay is one part of the Total Rewards that Medidata provides to compensate and recognize employees for their work. Most sales positions are eligible for a commission on the terms of applicable plan documents, and many of Medidata's non-sales positions are eligible for annual bonuses. Medidata believes that benefits should connect you to the support you need when it matters most and provides benefits, including medical, dental, life and disability insurance, 401(k) matching, family leave, flexible paid time off; and 10 paid holidays per year.
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#LI-Remote
Note: Please be on the lookout for job scams. Medidata recruiters will never ask applicants for monetary compensation, credit card, or banking details.
Equal Employment Opportunity:
In order to provide equal employment and advancement opportunities to all individuals, employment decisions at Medidata are based on merit, qualifications and abilities. Medidata is committed to a policy of non-discrimination and equal opportunity for all employees and qualified applicants without regard to race, color, religion, gender, sex (including pregnancy, childbirth or medical or common conditions related to pregnancy or childbirth), sexual orientation, gender identity, gender expression, marital status, familial status, national origin, ancestry, age, disability, veteran status, military service, application for military service, genetic information, receipt of free medical care, or any other characteristic protected under applicable law. Medidata will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
We will accept applications on an ongoing basis until we fill the position.