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International Remote Biomedical Jobs (NOW HIRING)

Lead Quality Engineer

Redwood City, CA · On-site +1

$120K - $165K/yr

... such as Biomedical, Bioengineering or Chemical Engineering * Experience with applicable FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Lead Quality Engineer

New York, NY · On-site +1

$120K - $165K/yr

... such as Biomedical, Bioengineering or Chemical Engineering * Experience with applicable FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Lead Quality Engineer

Chicago, IL · On-site +1

$120K - $165K/yr

... such as Biomedical, Bioengineering or Chemical Engineering * Experience with applicable FDA ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Sr. Program Manager

Irvine, CA · On-site +1

$124K - $125K/yr

Willingness to travel 10-20% (domestic and international) * Proficiency in Excel, financial ... Remote or field-based positions will have different workplace arrangements which will be indicated ...

This may include electronic/electrical, electro-mechanical or biomedical engineering or medical ... BSI offers a competitive total reward package, an independent and varied job in an international ...

This may include electronic/electrical, electro-mechanical or biomedical engineering or medical ... BSI offers a competitive total reward package, an independent and varied job in an international ...

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Showing results 1-20

International Remote Biomedical information

See salary details

$15

$28

$38

How much do international remote biomedical jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for international remote biomedical in the United States is $28.53, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $32.21 per hour, depending on experience, location, and employer.

What is the difference between International Remote Biomedical vs International Remote Medical Laboratory Technician?

AspectInternational Remote BiomedicalInternational Remote Medical Laboratory Technician
Required CredentialsBachelor's in Biomedical Science or related field, certifications varyAssociate's or Bachelor's in Medical Laboratory Technology, relevant certifications
Work EnvironmentRemote, research-focused, data analysisRemote, laboratory data processing, sample management
Employer & Industry UsageResearch institutions, biotech companies, healthcareHospitals, diagnostic labs, healthcare providers
Common Search & ComparisonYesNo

International Remote Biomedical roles typically involve research, data analysis, and development in biotech or healthcare sectors, requiring a biomedical background. In contrast, International Remote Medical Laboratory Technicians focus on lab data management and sample processing, often needing specific laboratory technology certifications. Both roles are remote and industry-related but differ in daily tasks and credential requirements.

What is an International Remote Biomedical professional?

An International Remote Biomedical professional is someone who works in the biomedical field, such as biomedical engineering or research, while operating remotely from a location different from where the healthcare or research facility is based. These professionals may collaborate with global teams to develop, test, or maintain medical devices, analyze biomedical data, or support healthcare technology projects across borders. Their work often involves using digital tools and communication platforms to bridge geographical gaps, ensuring effective contribution to international biomedical projects.

What are the key skills and qualifications needed to thrive as an International Remote Biomedical Specialist, and why are they important?

To thrive as an International Remote Biomedical Specialist, you typically need a degree in biomedical engineering or a related field, along with strong analytical and problem-solving skills. Familiarity with medical device software, remote diagnostic tools, and international regulatory standards is highly valuable. Excellent communication, cultural sensitivity, and self-motivation are crucial soft skills for collaborating across global teams and supporting clients remotely. These competencies ensure effective technical support, regulatory compliance, and seamless operations in diverse, international healthcare environments.

What are some common challenges faced by International Remote Biomedical professionals, and how can they be addressed?

International Remote Biomedical professionals often face challenges such as coordinating across different time zones, navigating diverse regulatory requirements, and ensuring effective communication with global teams. To address these, it's important to utilize robust digital collaboration tools, stay updated on international compliance standards, and develop strong cross-cultural communication skills. Regular virtual meetings, clear documentation, and a proactive approach to problem-solving can further help maintain project momentum and foster successful international collaborations.
More about International Remote Biomedical jobs
What cities are hiring for International Remote Biomedical jobs? Cities with the most International Remote Biomedical job openings:
What states have the most International Remote Biomedical jobs? States with the most job openings for International Remote Biomedical jobs include:
Infographic showing various International Remote Biomedical job openings in the United States as of May 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 21% Full Time, and 77% Part Time. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $59,333 per year, or $28.5 per hour.

Regional Clinical Trial Manager - East Coast, US

Prilenia

Remote

Full-time

Posted 29 days ago


Job description

About Prilenia
Prilenia, a private biopharmaceutical company with a highly committed and talented global team, is seeking a Regional Clinical Trial Manager located in the US.
Prilenia has a simple but urgent mission - to bring transformative medicines to people affected by devastating neurodegenerative diseases. Unwavering in our commitment to scientific excellence, Prilenia is developing pridopidine, a unique, oral, sigma-1 receptor (S1R) agonist investigational neuroprotective therapy for ALS and Huntington's disease (HD). Partnered with Ferrer for the commercialization and co-development of pridopidine, we plan to start two key late-stage trials to support potential approval globally in ALS and in HD in the first half of 2026.
To learn more about our story and company culture, visit us at https://Prilenia.com
About the role
We are seeking a dynamic Regional Clinical Trial Manager to join our team and to oversee and manage regional operational activities of global pivotal trial/s in neurodegeneration. The ideal candidate will bring deep clinical research experience with extensive experience in clinical project management and a proven track record in managing global pivotal clinical trials for biotech sponsors and support clinical operations leadership to innovate and continuously improve operational standards. Experience in rare diseases required, HD and/or ALS preferred. This is a critical individual contributor role in a growing biotech company, suitable for a candidate who is equally comfortable working independently across multiple projects and while collaborating in a matrix global team environment. The position will report to the SVP, Head of Clinical Operations.
Roles and Responsibilities:
  • Responsible for the oversight and management of operational activities in given regional area. Including but not limited to: multi studies regional supervision from Phase I-III, multi centers visits Ad Hoc.
  • Develop and oversee procedures for dealing with troubleshooting and problem solving.
  • Establish and monitor programs/protocols/procedures. Including but not limited to: supervision of full protocol procedures on site, joining Trainings and Visits on a routine base.
  • Support the evaluation of suitability of site personnel and facility for initial and ongoing conduct of clinical trial
  • Maintain appropriate and effective communication with vendors and other internal departments to ensure successful project completion
  • Build and sustain strong cross-functional relationships across diverse global teams; foster a culture of mutual accountability, collaboration, and innovation.
  • Communicate progress, risks, and strategic insights to executive leadership and governance committees, supporting data-driven decision-making and program advancement.

Qualifications and Skills:
  • Bachelor's degree required, preferably in science, nursing, other life sciences, biomedical discipline, or equivalent. Advanced degree preferred.
  • Minimum 7-10 years clinical research experience as a CRA or equivalent, such as research coordinator with of 3 years of clinical project management experience or Operations management or equivalent.
  • Demonstrated Clinical Monitoring and/or Data Management experience required.
  • Recent experience in leading the conduct of global phase 3 studies from start to completion required.
  • Experience with rare diseases required Experience with ALS or HD highly preferred Excellent understanding and demonstrated application of FDA guidelines, Good Clinical Practices (GCP), ICH and applicable Standard Operating Procedures.
  • Strong project management skills, stakeholder management and communication skills, including influencing executive leadership, cross-functional partners, and external collaborators.
  • Displays exceptional situational awareness in communication-adapts tone, content, and level of detail to suit the audience, from executives to technical teams. Demonstrates sound judgement in deciding what details to share or escalate.
  • Excellent problem-solving and decision-making skills.
  • Demonstrated Budget management skills required.
  • Ability to work independently, prioritize and work within a matrix team environment is essential. Ability to work across multiple projects with demonstrated ability to manage CROs (and other vendors) to meet or exceed KPIs tied to corporate goals and hold them accountable if they fall behind.
  • Proficiency with clinical research technologies and platforms (EDC, eTMF, IWRS, CTMS, etc.), plus strong skills in Microsoft Office and data analysis tools.
  • Willingness and ability to travel (domestic & international) and operate flexibly in virtual teams and global time zones. Travel up to 50% (regional).

Location/Time Zones:
  • This is a full-time, remote position in the US.
  • Expected domestic/regional travel up to 50% with some international travel.
  • Flexible schedule with interactions across North America, Europe and Israel time zones.

Prilenia operates across the United States, Canada, Europe and Israel, is incorporated in the Netherlands and backed by leading life sciences investors. We are a highly flexible organization that is mostly remote and encourages team members to work in the ways that make them most effective, with a focus on our common goals and getting the job done.
Prilenia is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. We are dedicated to fostering a diverse, inclusive, and welcoming workplace for all.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.