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Virtual Biomedical Engineer Internship Jobs in Dallas, TX

Smiths Group

Engineer III Materials

Irving, TX · On-site

... Engineering, Biomedical Engineering or a related field and 5 years of progressive, post ... Position requires completion of a university-level course, research project, internship, or thesis ...

Smiths Group

Engineer III Materials

Irving, TX · On-site

... Engineering, Biomedical Engineering or a related field and 5 years of progressive, post ... Position requires completion of a university-level course, research project, internship, or thesis ...

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All JobsBiomedical Engineer JobsVirtual Biomedical Engineer Internship JobsVirtual Biomedical Engineer Internship Jobs in Dallas, TX

Virtual Biomedical Engineer Internship information

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How much do virtual biomedical engineer internship jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for virtual biomedical engineer internship in Dallas, TX is $25.14, according to ZipRecruiter salary data. Most workers in this role earn between $20.43 and $28.56 per hour, depending on experience, location, and employer.

What is a virtual biomedical engineer internship?

A Virtual Biomedical Engineer Internship is a remote work experience where students or recent graduates gain practical exposure to biomedical engineering tasks and projects through online platforms. Interns typically assist in designing medical devices, analyzing biomedical data, or supporting research and development teams—all while working from home or another remote location. This format allows interns to collaborate with professionals, develop technical skills, and contribute to healthcare innovations without needing to be physically present in a laboratory or office. Such internships are ideal for those seeking flexibility or who are unable to relocate. They often involve communication via video calls, email, and project management tools.

What are the key skills and qualifications needed to thrive as a virtual biomedical engineer intern?

To thrive as a Virtual Biomedical Engineer Intern, you need a solid background in biomedical engineering principles, problem-solving, and data analysis, generally supported by enrollment in or completion of a relevant engineering degree program. Familiarity with computer-aided design (CAD) tools, simulation software, and basic programming languages like MATLAB or Python is often expected. Strong communication, self-motivation, and adaptability are crucial soft skills in a remote environment. These skills and qualities enable you to effectively contribute to project goals, collaborate remotely with diverse teams, and adapt to evolving technical challenges in the biomedical field.

What types of projects and team collaborations can I expect during a virtual biomedical engineer internship?

As a virtual biomedical engineer intern, you’ll typically work on projects like designing medical device prototypes, analyzing biomedical data, or conducting literature reviews on emerging technologies. You’ll frequently collaborate with multidisciplinary teams—including engineers, researchers, and clinicians—using digital communication tools for meetings and project management. Expect regular check-ins with mentors, participation in group brainstorming sessions, and opportunities to present your findings. The virtual format emphasizes strong communication, self-management, and proactive engagement with team members to ensure project success.

What is the difference between Virtual Biomedical Engineer Internship vs Virtual Biomedical Technician Internship?

AspectVirtual Biomedical Engineer InternshipVirtual Biomedical Technician Internship
Required CredentialsTypically requires a biomedical engineering background or related degreeOften requires technical training or certification in medical equipment
Work EnvironmentRemote, project-based, involving design and development tasksRemote or on-site, focusing on maintenance and troubleshooting
Employer & Industry UsageUsed by medical device companies, research institutions, and healthcare tech firmsCommon in hospitals, clinics, and medical equipment service providers

The Virtual Biomedical Engineer Internship focuses on designing and developing medical devices and systems, requiring engineering skills. In contrast, the Virtual Biomedical Technician Internship emphasizes maintenance, troubleshooting, and repair of medical equipment. Both roles are valuable in healthcare technology, but they differ in responsibilities and skill requirements.

What are popular job titles related to Virtual Biomedical Engineer Internship jobs in Dallas, TX?

For Virtual Biomedical Engineer Internship jobs in Dallas, TX, the most frequently searched job titles are:

What job categories do people searching Virtual Biomedical Engineer Internship jobs in Dallas, TX look for?

The top searched job categories for Virtual Biomedical Engineer Internship jobs in Dallas, TX are:

What cities near Dallas, TX are hiring for Virtual Biomedical Engineer Internship jobs?

Cities near Dallas, TX with the most Virtual Biomedical Engineer Internship job openings:

Virtual Biomedical Engineer Internship jobs near you
Infographic showing various Virtual Biomedical Engineer Internship job openings in Dallas, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 90% In-person, 5% Hybrid, and 5% Remote job distribution, with an average salary of $52,298 per year, or $25.1 per hour.

Clinical Research Associate (Biomedical Engineering Candidates)

Medpace, Inc.

Irving, TX • On-site

Other

Medical, Retirement, PTO

Posted 21 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

13th of 74 rated research

Job description

Job Summary
Join our CRA Team in Dallas, TX!
We are hiring those with Biomedical Engineering backgrounds for the CRA role!
The Clinical Research Associate position offers an exciting career within clinical research! For those with biomedical engineering backgrounds wanting to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!
This position is office based in Dallas, TX.
Medpace CRA Training Program (PACE®)
No prior research experience is needed, as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. The PACE® (Professionals Achieving CRA Excellence) Training Program includes the following:
  • A platform to effectively and confidently carry out CRA duties to ultimately become a high-functioning, independent, Medpace CRA
  • Interactive discussions with hands-on exercises and practicums
  • Core departmental rotations to learn various aspects of the drug/device development and approval process

Why CRA?
  • Exciting travel opportunities
  • Make a difference on a larger scale through the development of medical drugs and devices
  • Dynamic working environment with varying day-to-day responsibilities
  • Exposure to multiple therapeutic areas
  • Defined CRA promotion and growth ladder

We Offer the Following:
  • Competitive travel bonus
  • Equity/Stock option program
  • Training completion and retention bonus
  • Annual merit increases
  • 401K matching
  • Opportunity to work from home
  • Flexible work hours across days within a week
  • Retain airline reward miles and hotel reward points
  • Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
  • In-house travel agents, reimbursement for airline club membership, and TSA pre-check
  • Opportunity for leadership positions - Lead CRA, CRA Manager, Training and Development Manager, and many more
  • CRA training program - PACE®
  • Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
  • In-house administrative support for all levels of CRA
  • Opportunity to work with international team of CRAs

Responsibilities
  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
  • Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
  • Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
  • Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
  • On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward
  • Verification the investigator is enrolling only eligible subjects
  • Regulatory document review
  • Medical device and/or investigational product/drug accountability and inventory
  • Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
  • Assess the clinical research site's patient recruitment and retention success and offering suggestions for improvement
  • Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications
  • Minimum of a Bachelor's degree in a health or science related field; degree in Biomedical Engineering preffered
  • Ability to travel 60-70% to locations nationwide is required
  • A valid driver's license and the ability to drive to monitoring sites
  • Minimum 1 year healthcare-related work experience preferred
  • Proficient knowledge of Microsoft Office
  • Strong communication and presentation skills
  • Detail-oriented and efficient in time management

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events

Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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