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Biomedical Scientist In Japan Jobs in Delaware (NOW HIRING)

Clinical Affairs Scientist

Wilmington, DE · On-site +1

$105K - $197K/yr

D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred. * 4+ years of experience in IVD product development, clinical research, medical writing, and/or ...

Posted today

$56K - $65K/yr

Associate's in the following programs or related programs - Computer Science, Electrical Engineering, Biomedical Electronics, System Administration, Computer Programming, Computer Networking ...

Bachelor's Degree in Chemistry, Biology, Biochemistry, Chemical/Bioengineering, Biomedical Engineering, Materials Science, or related field with 3-5 years of experience, OR * Associate's Degree with ...

About Fujifilm Celebrating our 90th anniversary in 2024, Japan's pioneering photographic film maker ... science, technology and industry, as well as improved health and environmental protection in ...

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About Fujifilm Celebrating our 90th anniversary in 2024, Japan's pioneering photographic film maker ... science, technology and industry, as well as improved health and environmental protection in ...

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About Fujifilm Celebrating our 90th anniversary in 2024, Japan's pioneering photographic film maker ... science, technology and industry, as well as improved health and environmental protection in ...

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About FujifilmCelebrating our 90th anniversary in 2024, Japan's pioneering photographic film maker ... science, technology and industry, as well as improved health and environmental protection in ...

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Biomedical Scientist In Japan information

What is a biomedical scientist in Japan?

Biomedical Scientists in Japan are professionals who conduct research and perform laboratory tests to help diagnose, treat, and prevent diseases. They work in hospitals, research institutes, and universities, focusing on areas such as pathology, genetics, microbiology, and clinical chemistry. Their work supports medical practitioners by providing critical data for patient care and advancing scientific knowledge in healthcare. In Japan, becoming a biomedical scientist typically requires a relevant degree and, in many cases, specialized training or certification. The profession is integral to the Japanese healthcare system and medical research community.

What are the key skills and qualifications needed to thrive as a biomedical scientist in Japan?

To thrive as a Biomedical Scientist in Japan, you need a strong background in biology, chemistry, and laboratory science, typically supported by a relevant degree and national certification. Familiarity with advanced laboratory equipment, diagnostic software, and adherence to Japanese clinical laboratory standards is crucial. Attention to detail, analytical thinking, and effective communication are valuable soft skills for ensuring accurate results and collaborating with healthcare teams. These competencies are essential for maintaining high-quality diagnostic services and supporting patient care in Japan's healthcare system.

What are the typical collaboration opportunities for a biomedical scientist working in Japan?

Biomedical Scientists in Japan often collaborate closely with multidisciplinary teams, including medical doctors, engineers, and pharmaceutical researchers. These collaborations commonly occur in hospital laboratories, research institutes, and universities, where joint projects aim to advance diagnostic techniques or develop new medical devices. Effective communication and teamwork are essential, as many projects require integrating clinical perspectives with laboratory findings. Additionally, there are opportunities to participate in international research collaborations, given Japan’s strong emphasis on global scientific exchange.

What is the difference between Biomedical Scientist In Japan vs Medical Laboratory Technician In Japan?

AspectBiomedical Scientist In JapanMedical Laboratory Technician In Japan
Required CredentialsBachelor's degree in biomedical sciences, certification/licenseDiploma or associate degree, certification/license
Work EnvironmentResearch labs, hospitals, diagnostic labsHospital labs, clinics, diagnostic centers
Employer & Industry UsageResearch institutions, hospitals, biotech companiesHospitals, diagnostic labs, clinics
Common Search & ComparisonOften compared for roles in diagnostics and researchOften compared for technical lab work

In Japan, Biomedical Scientists typically hold higher qualifications and work in research or advanced diagnostic settings, while Medical Laboratory Technicians focus on routine testing in clinical labs. Both roles are essential but differ in scope and responsibilities.

How much do biomedical scientists make in Japan?

Biomedical scientists in Japan typically earn between 4 million and 6 million yen annually, depending on experience, qualifications, and location. Entry-level positions may start lower, while experienced professionals with specialized skills can earn higher salaries, often supplemented by benefits and research opportunities.

What are popular job titles related to Biomedical Scientist In Japan jobs in Delaware?

For Biomedical Scientist In Japan jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Biomedical Scientist In Japan jobs in Delaware look for?

The top searched job categories for Biomedical Scientist In Japan jobs in Delaware are:

What cities in Delaware are hiring for Biomedical Scientist In Japan jobs?

Cities in Delaware with the most Biomedical Scientist In Japan job openings:

Clinical Affairs Scientist

Agilent

Wilmington, DE • On-site, Remote

$105K - $197K/yr

Full-time

Posted 22 hours ago

Posted today


Agilent Technologies rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

48th of 543 rated manufacturers


Job description

Job Description

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports.
Responsibilities include but are not limited to:

  • Provide thought leadership on key relevant clinical topics to support strategy development and execution.

  • Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies.

  • Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

  • Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials.

  • Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data.

  • Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).

  • Provide clinical and scientific oversight of local marketing and commercial materials.

  • Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies.

  • Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies.

  • Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations.

  • Support audits and inspections as a clinical subject matter expert.

Qualifications
  • Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred.

  • 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry.

  • Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice preferred.

  • Ability to interpret regulatory standards, guidance, and laws.

  • Strong scientific, medical writing, and presentation skills

  • Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

  • Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

  • Experience working with external partners and/or regulatory bodies including the FDA.

  • Knowledge in oncology, immunology, and/or pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Medical/Clinical

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