Philips

6 days ago

Clinical Development Scientist, Ultrasound &EI

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 11 hours agoStatus: Live

Job Summary

Execute evidence generation and clinical development activities for New Product Introduction (NPI) projects and post-market work in Greater China. Assess clinical trial protocols, refine study designs, and develop clinical documentation including CERs, CSRs, and regulatory submission sections. Collaborate with stakeholders across marketing/BU claims, health economics, market access, and post-market surveillance, while maintaining data integrity and performing scientific literature reviews to support strategic decision-making.

Location: Shanghai

Workplace: Onsite

Employment Type: Full time

Job Function: Research & Scientific (R&D)

Seniority: Mid level

Key Responsibilities

•Assess clinical trial protocols and studies, ensuring alignment with regulatory standards and business objectives, and contribute to study design refinement under direct supervision.
•Execute clinical development and market access strategies for assigned NPI projects and post-market activities, integrating stakeholder inputs.
•Draft comprehensive and compliant Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and clinical sections of regulatory submissions.
•Troubleshoot clinical data collection, analysis, and reporting issues to ensure data integrity and accuracy and maintain study outcomes.
•Conduct rigorous literature searches and critical reviews to support evidence-generation processes and strategic decision-making.

Pay and Benefits

Perks:Health InsuranceWellness Stipend

Key Requirements

•Master or PhD in medical science, clinical medicine, Biomedical, or equivalent.
•Minimum 2 years of relevant industry experience (e.g., Med. Device field).
•Minimum 2 years of experience in clinical evaluation or clinical research.
•Excellent English speaking and writing.
•Strong knowledge of regulatory requirements, regulation compliance, and clinical evaluation methodologies with data analysis and interpretation.

Experience:2+ yearsMedical devicesClinical researchRegulatory submissions

Education:PhD / Doctorate in medical science or clinical medicine or Biomedical

Skills:English communicationRegulation complianceData analysisScientific literature reviewsAttention to detail

Languages:English

Tech Stack:NPIPLMPMS

Company Brief

Philips

Global health technology company focusing on diagnostic imaging, patient monitoring, and consumer health products. Philips develops medical devices, healthcare informatics, and solutions to improve patient care and personal well-being.

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Amsterdam, Netherlands

Founded: 1891

Glassdoor: 3.8

Website LinkedIn

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Philips

6 days ago

Clinical Development Scientist, Ultrasound &EI

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 11 hours agoStatus: Live

Job Summary

Location: Shanghai

Workplace: Onsite

Employment Type: Full time

Job Function: Research & Scientific (R&D)

Seniority: Mid level

Key Responsibilities

•Assess clinical trial protocols and studies, ensuring alignment with regulatory standards and business objectives, and contribute to study design refinement under direct supervision.
•Execute clinical development and market access strategies for assigned NPI projects and post-market activities, integrating stakeholder inputs.
•Draft comprehensive and compliant Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and clinical sections of regulatory submissions.
•Troubleshoot clinical data collection, analysis, and reporting issues to ensure data integrity and accuracy and maintain study outcomes.
•Conduct rigorous literature searches and critical reviews to support evidence-generation processes and strategic decision-making.

Pay and Benefits

Perks:Health InsuranceWellness Stipend

Key Requirements

•Master or PhD in medical science, clinical medicine, Biomedical, or equivalent.
•Minimum 2 years of relevant industry experience (e.g., Med. Device field).
•Minimum 2 years of experience in clinical evaluation or clinical research.
•Excellent English speaking and writing.
•Strong knowledge of regulatory requirements, regulation compliance, and clinical evaluation methodologies with data analysis and interpretation.

Experience:2+ yearsMedical devicesClinical researchRegulatory submissions

Education:PhD / Doctorate in medical science or clinical medicine or Biomedical

Skills:English communicationRegulation complianceData analysisScientific literature reviewsAttention to detail

Languages:English

Tech Stack:NPIPLMPMS

Company Brief

Philips

Industry: HealthTech

Company Size: Enterprise (1,001+ employees)

Revenue: USD 1B+

Growth: Public Company

Valuation: Public Company (Market Cap in USD)

Funding: IPO / Publicly Listed

Headquarters: Amsterdam, Netherlands

Founded: 1891

Glassdoor: 3.8

Website LinkedIn