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Medical Device Research Jobs in Georgia (NOW HIRING)

Artivion

R&D Intern (Part-Time)

Kennesaw, GA · On-site

$13.75 - $18.50/hr

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on ... To provide current college students the opportunity to gain hands-on research and development ...

CryoLife

R&D Intern (Part-Time)

Kennesaw, GA · On-site

$13.75 - $18.50/hr

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on ... To provide current college students the opportunity to gain hands-on research and development ...

BSI Prof Serv EHS West

EMEA/UK- Homebased BSI is seeking R&D Scientists and Production Scientists to join our IVD Devices ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

BSI Group

EMEA/UK- Homebased BSI is seeking R&D Scientists and Production Scientists to join our IVD Devices ... Provide Medical Device QMS assessment and device expertise leadership and mentoring in areas of ...

Avanos Medical

R&D Engineer III

Alpharetta, GA · On-site

Avanos is a medical device company focused on delivering clinically superior breakthrough solutions ... Avanos is seeking an R&D Engineer III to support the design, development, testing, documentation ...

BSI Prof Serv EHS West

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

BSI Group

If you have hands-on experience in the research, design, manufacture or testing of active devices we'd love to hear from you. As a Technical Reviewer, you will work with medical device manufacturers ...

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... The ideal candidate will have cardiovascular medical device monitoring experience- however, complex ...

Centricity Research

Clinical Screening Coordinator

Rincon, GA · On-site

$22 - $29.25/hr

... medical device trials. About the Role We're looking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in ...

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Medical Device Research information

What is medical device research?

Medical device research involves the development, testing, and evaluation of medical devices to ensure their safety, effectiveness, and regulatory compliance before they reach the market. This research covers a range of activities, including preclinical studies, clinical trials, and post-market surveillance. Professionals in this field work closely with engineers, healthcare providers, and regulatory bodies to develop innovations that improve patient care.

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

To excel in Medical Device Research, a strong background in biomedical engineering, life sciences, or a related field is essential, often accompanied by advanced degrees. Familiarity with regulatory standards (such as FDA or ISO), clinical trial management systems, and data analysis tools is highly valuable. Exceptional problem-solving, teamwork, and attention to detail help professionals innovate and navigate complex project requirements. These skills are crucial for ensuring rigorous research, regulatory compliance, and the successful development of safe and effective medical devices.

What are some typical challenges faced by professionals working in medical device research?

Professionals in Medical Device Research often encounter challenges such as navigating complex regulatory requirements, ensuring patient safety during clinical trials, and meeting strict documentation standards. Balancing innovation with compliance can be demanding, as teams must integrate new technologies while adhering to FDA or international regulations. Effective collaboration with cross-functional teams—including engineers, clinicians, and regulatory specialists—is essential to address these challenges and drive projects toward successful approval and market release.
Medical Device Research jobs near you
Infographic showing various Medical Device Research job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 15% Part Time, 11% Contract, and 3% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Clinical Research Associate (CRA) -Cardiovascular Medical Device

Mirus LLC

Marietta, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 14 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%