Medical Affairs Specialist (Pathology Support, EU)

TN France; France; Sur place; EUR 60 000 - 100 000; Plein temps

Résumé du poste

An established industry player is seeking a Medical Affairs Specialist to join their dynamic team in the field of Precision Medicine. This role involves engaging with pathologists and healthcare providers to highlight the clinical value of innovative products. The ideal candidate will possess extensive experience in oncology diagnostics and demonstrate strong interpersonal and presentation skills. This position offers the opportunity to contribute to groundbreaking advancements in healthcare while collaborating with cross-functional teams. If you're passionate about making a difference in patient outcomes, this role is perfect for you.

Qualifications

• 5+ years in medical affairs with pharma or diagnostics.
• Strong background in diagnostics and oncology biomarkers.

Responsabilités

• Engage with KOLs to develop professional relationships.
• Provide scientific support for product development and marketing.
• Conduct presentations and training for teams and collaborators.

Connaissances

Medical Affairs

Oncology-based Biomarkers

In Vitro Diagnostics

Presentation Skills

Interpersonal Skills

Data Analysis

Formation

Degree in Life Sciences

Degree in Pharmacology

Description du poste

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Medical Affairs Specialist (Pathology Support, EU), France

Client: Agilent

Location: France

Job Category: Customer Service

EU work permit required: Yes

Job Reference: fd12f6dd4fd0

Job Views: 2

Posted: 03.05.2025

Expiry Date: 17.06.2025

Job Description:

Description

Become a part of a growing and dedicated team that does truly inspiring work in the field of Precision Medicine. Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Information about Agilent is available at .

We are searching for an experienced Medical Affairs Specialist to work within the exciting field of Biomarkers testing, molecular diagnostics and digital pathology. As a Medical Affairs Specialist, you will proactively engage with practicing pathologists and other healthcare providers to establish the clinical value of Agilent’s products, identify evidence gaps and implement remediation activities. To be successful, you will have a strong background in diagnostics and experience working with oncology-based biomarkers or in vitro diagnostics. Additional responsibilities include support of external quality assessment organizations/programs (such as CAP, UK NEQAS, NordiQC, and QuiP).

Responsibilities:

• Engage with key opinion leaders (KOLs) to develop strong professional relationships
• Provide scientific and clinical support for product development and marketing strategies
• Conduct presentations and training for internal teams and external collaborators
• Act as a scientific resource for healthcare professionals and answer medical inquiries
• Support clinical trial activities and data dissemination
• Collaborate with cross-functional teams including marketing, sales, and regulatory affairs
• Supervise and report on competitive intelligence in the scientific community
• Develop and implement RWE generation strategic plans to address scientific gaps and opportunities
• Participate in medical and scientific conferences to represent the company
• Ensure compliance with regulatory and ethical guidelines in all scientific communications
• Write, review, and present medical communications documents (abstracts, posters, slide decks, whitepapers)
• Analyze and interpret data from EQA programs to influence clinical practices, patient outcomes, and regulatory compliance.

Qualifications

Required Qualifications:

• Degree or equivalent in Life Sciences, Pharmacology, or related fields
• 5+ years of professional experience in medical affairs working with pharma, diagnostics, or companion diagnostics in oncology, pathology, or NGS liquid biopsy
• In-depth skills acquired through training, study, and experience in diagnostics
• Proficiency in English (written and spoken)
• Strong presentation and interpersonal skills
• Experience in investigator-initiated studies or RWE generation
• Willingness to travel globally (approx. 25-35%)
• Ability to work independently and manage multiple projects

Preferred Qualifications:

• Experience in a Life Science diagnostic company, in Patient Safety, Medical Affairs, Clinical Research, or Medical Science Liaison roles (preferred but not required)
• Previous scientific publications (preferred but not required)
• Understanding of industry standards, laws, and regulations (preferred but not required)
• Experience with EQA organizations or participation in EQA programs (highly desired)
• Knowledge of EU regulations and guidelines for IVD and companion diagnostics (preferred)

Preferred location is Europe (Germany, Spain, France, Italy, Switzerland), but other locations and remote work are considered for well-qualified candidates.