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Internship Medical Device Clinical Research Jobs

Bright Uro

RD Internship Medical Device Company

Irvine, CA · On-site

$18 - $23.25/hr

... for clinicians to gain actionable insights while delivering a better patient experience. Our ... Project involvement in Research & Development, manufacturing support, or robotics * Device design ...

Provident Research Inc

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Senior Clinical Research Associate Cardiac Medical Device

Phoenix, AZ · Remote

$135K - $141K/yr

SR CRA Cardiac Medical Device (home based) Remote Become Part of a Major Initiative to Monitor Life ... clinical research areas Relevant industry certifications preferred (i.e. CCRA, RAC, CDE ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ · On-site

$95K - $115K/yr

Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research ...

Iota Biosciences

Manager, Clinical Operations

Alameda, CA · On-site

$145K - $200K/yr

Minimum 8+ years of relevant clinical research experience in the medical device field, or an advanced degree with a minimum of 5 years of relevant experience in the medical device field * At least 3 ...

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Internship Medical Device Clinical Research information

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How much do internship medical device clinical research jobs pay per month?

As of Aug 9, 2026, the average monthly pay for internship medical device clinical research in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in an internship in medical device clinical research?

To thrive in an Internship Medical Device Clinical Research role, you need a solid grounding in life sciences or biomedical engineering, along with familiarity with clinical research methodologies and regulatory guidelines. Experience with data management systems, statistical analysis software, and an understanding of Good Clinical Practice (GCP) are commonly required. Strong attention to detail, communication skills, and the ability to collaborate effectively within multidisciplinary teams are vital soft skills. These qualifications ensure accurate research execution, regulatory compliance, and productive teamwork, all of which are crucial for successful clinical studies and device development.

What types of projects or tasks can I expect to work on during an internship in medical device clinical research?

As an intern in Medical Device Clinical Research, you may assist with tasks such as supporting clinical trial documentation, helping to manage patient data, preparing regulatory submissions, and coordinating study logistics. You'll likely collaborate with cross-functional teams including regulatory affairs, data management, and clinical operations. This hands-on experience will give you insight into the end-to-end process of bringing a medical device from development through clinical validation, while also building your understanding of regulatory standards and good clinical practice.

What is an internship in medical device clinical research?

An Internship in Medical Device Clinical Research is a temporary position, often for students or recent graduates, that provides hands-on experience in the processes involved in testing and evaluating medical devices for safety and effectiveness through clinical trials. Interns typically assist with study documentation, data collection, regulatory compliance, and communication with clinical sites. This role offers valuable exposure to clinical research protocols and the medical device industry, helping interns develop professional skills and knowledge relevant to regulatory standards and product development.

How to become an internship medical device clinical research?

To become an intern in medical device clinical research, candidates typically need a background in healthcare, life sciences, or engineering, along with strong analytical and communication skills. Relevant experience can be gained through coursework, certifications such as GCP (Good Clinical Practice), and internships in related fields. Applying to companies or research organizations that offer internship programs and demonstrating knowledge of clinical trial processes are essential steps.
What cities are hiring for Internship Medical Device Clinical Research jobs? Cities with the most Internship Medical Device Clinical Research job openings:
What are the most commonly searched types of Medical Device Clinical Research jobs? The most popular types of Medical Device Clinical Research jobs are:
What states have the most Internship Medical Device Clinical Research jobs? States with the most job openings for Internship Medical Device Clinical Research jobs include:
Internship Medical Device Clinical Research jobs near you

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Job description


Role: Clinical Research Associate (CRA) - Cardiovascular Medical Device

Location: Remote

Position Summary:

Assist with the management of cardiovascular clinical studies for MiRus products with a focus on adherence to critical timelines, high-caliber document development and quality data collection. The applicant should possess strong critical thinking skills and the ability to comprehend technical subject matter to effectively contribute to the organization.

Essential Duties and Responsibilities:

  • Contribute to content generation, writing and editing of study protocols, amendments, informed consents, committee charters, study reports, monitoring plans, and other related clinical and regulatory documents.
  • Assist with the management of investigational studies from start through study closure.
  • Engage in new study trial design with cross functional teams, including clinical and pre-clinical research and development groups.
  • Contribute to the development of CRFs
  • Assist with the formulation of instructional materials and training of investigators, study coordinators and associated study site personnel on the conduct of the clinical trials, as applicable.
  • Assist Study Manager with safety monitoring including preparing supporting documentation for CEC and/or DSMB, meetings, agenda, data review, presentations, and updating relevant trackers as applicable.
  • Serve as a point of contact between clinical site investigators and the MiRus team.
  • Work with investigators and site personnel to quickly and effectively resolve discrepancies.
  • May be responsible for patient accruals and tracking payments to sites for clinical study programs
  • Serve as a point of contact between CRO personnel and MiRus.
  • Oversee/support CRO and field study monitors, with monitoring related items and follow-up on study tasks.
  • Monitor ongoing compliance to study protocols in accordance with applicable regulations and GCP, work instructions, guidelines and/or policies.
  • Provide continuous data review of source documents, case report forms, data reports as appropriate.
  • Assist in review of monitoring reports and tracking of action items.
  • Review source documentation to confirm subject eligibility for clinical trials.
  • Track and upload study imaging
  • Manage clinical study documentation (trial master file and study related tracking).
  • Update and design as needed study dashboards, study trackers and other applicable study documents to provide regular updates on trial status to Study Manager
  • Interact with data management, as applicable
  • Support applications and technical files as needed.
  • Assist with preparation for investigators meetings.

Minimum Education and/or Experience:

  • Bachelor’s or Master’s degree in nursing with clinical experience in the cardiac field (CCU, CVOR, Cath Lab) and experience in a clinical research role. CRA certification desired.
  • At least 2 years of experience in clinical research role, with at least 2 years in CRA role, preferably in cardiovascular medical device.
  • Experience in clinical trials and/or post-market registries in the U.S., Australian and/or European Union, with other geographies desired.
  • Current knowledge of medical device clinical trials design and best practices.
  • Proficient knowledge of FDA regulations and ICH/GCP guidelines, guidance documents, and other applicable regulations and standards, and implementation of these standards in the medical device industry, in the U.S. and all countries in which trials are conducted.
  • General application of medical terminology (cardiovascular specific preferred).

Benefits:
MiRus offers competitive compensation, options, full benefits, and relocation assistance.

  • 401(k)
  • Dental insurance
  • Vision insurance
  • Disability insurance
  • Employee assistance program
  • Flexible spending account or Health Savings Account
  • Health insurance
  • Life insurance
  • Paid time off

Schedule:

  • Monday to Friday (8am – 5pm)

Work Location:

  • Remote
  • Position may require domestic travel at least 20-40%