ZipRecruiter

Log In

1

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 ...

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

Minimum of 8 years of clinical affairs or clinical research experience within the medical device industry * Demonstrated leadership experience managing Clinical Affairs personnel, CROs, clinical ...

Noctrix Health

Director, Clinical Affairs

Pleasanton, CA · On-site

$89K - $121K/yr

Minimum of 8 years of clinical affairs or clinical research experience within the medical device industry * Demonstrated leadership experience managing Clinical Affairs personnel, CROs, clinical ...

Provident Research Inc

Be Seen First

Senior Clinical Research Associate Cardiac Medical Device

Phoenix, AZ · Remote

$135K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Provident Research Inc

Be Seen First

Senior Clinical Research Associate Cardiac Medical Device

Los Angeles, CA · Remote

$135K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Provident Research Inc

Be Seen First

Senior Clinical Research Associate Cardiac Medical Device

San Francisco, CA · Remote

$135K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Cleveland Diagnostics, Inc.

Clinical Study Manager

Cleveland, OH · On-site

$90K - $120K/yr

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in IVD or medical device clinical research strongly preferred. * Clinical research certification (e.g. ACRP, SOCRA) strongly preferred. * Knowledge of Good Clinical Practice (GCP)/ICH and ...

next page

Showing results 1-20

All Jobsinternship JobsScience JobsResearch JobsResearch Assistant JobsInternship Medical Device Clinical Research Jobs

Internship Medical Device Clinical Research information

See salary details

$2.1K

$6.4K

$7.8K

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

As of Aug 18, 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 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.

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 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 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

Senior Clinical Research Coordinator

Kyvexa Clinical Trials

Las Vegas, NV

$30/hr

Full-time

Posted 4 days ago

Job description

We are seeking an organized, detail-oriented Clinical Research Study Coordinator to join our team. The Study Coordinator will be responsible for the day-to-day management of clinical studies, including subject screening, informed consent, data entry, regulatory compliance, and coordination with investigators and sponsors. This role is ideal for candidates in research who want to grow in a dynamic, fast-paced clinical research environment.

Compensation 

  • Pay: $25 - $30 per hour based on experience and performance

Schedule

  • Monday to Friday

  • Full-time 

Compensation:

$25 - $30 hourly


Responsibilities:

  • Coordinate and conduct clinical trials according to GCP, ICH, FDA, and sponsor guidelines.

  • Recruit, screen, and enroll eligible study participants.

  • Obtain and document informed consent from subjects.

  • Perform study-related procedures such as specimen collection, vitals, or device use per protocol.

  • Schedule and manage subject visits, ensuring protocol adherence and accurate source documentation.

  • Enter data into Electronic Data Capture (EDC) systems and maintain study binders.

  • Maintain regulatory files, site logs, and documentation readiness for audits or monitoring visits.

  • Communicate with sponsors, CROs, monitors, and physicians regarding study progress and data queries.

  • Ensure subject confidentiality and compliance with HIPAA.

  • Assist in IRB submissions, amendments, and ongoing study correspondence.

  • Traveling required from Kyvexa headquarters to clinics around the Las Vegas Valley and vice versa


Qualifications:

  • Minimum of 1–2 years of clinical or research experience preferred (medical office or lab experience acceptable).

  • Knowledge of GCP, FDA, and ICH guidelines.

  • Strong organizational, multitasking, and time-management skills.

  • Excellent interpersonal and communication skills (bilingual English/Spanish preferred).

  • Computer proficiency with Microsoft Office and EDC systems.

  • Current CPR, Medical Assistant, and Phlebotomist certifications.


About Company

Kyvexa partners with sponsors and investigators to deliver reliable, patient-centered clinical trial site management for medical device research — combining regulatory rigor, operational excellence, and compassionate care to help bring safe, effective devices to market faster. At Kyvexa, we exist to make medical device clinical trials safer and more human — supporting patients, physicians, and sponsors with the highest standards of care, compliance, and integrity.