Full-Time Scientific Affairs Manager
Guardant Health is hiring a remote Full-Time Scientific Affairs Manager. The career level for this job opening is Manager and is accepting Worldwide based applicants remotely. Read complete job description before applying.
Guardant Health
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Scientific Affairs Manager (SAM)
The Scientific Affairs Manager is responsible for informing, engaging, and influencing key stakeholders at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health products. The SAM will pursue clinical data development, elevate Guardant's scientific relevance, and increase adoption of Guardant products. This includes influencing scientific presentations and publications, and translating complex genomic data for both biopharma and internal stakeholders.
Essential Duties and Responsibilities:
- Establish and maintain relationships with key stakeholders to elevate Guardant's reputation and foster potential collaborations.
- Engage with pharma stakeholders in scientific exchange to understand their oncology biomarker needs and educate them on data supporting Guardant products.
- Leverage expertise to influence pharma on oncology biomarker implementation and interpretation of Guardant data.
- Provide strategic review and edits for pharma partner materials (abstracts, posters, presentations, manuscripts).
- Identify and pursue collaboration opportunities with pharma and biotech companies aligned with Guardant's clinical data development strategy.
- Assess biopharma pipelines for Guardant engagement and research collaboration opportunities.
- Advocate for scientifically sound applications of ctDNA.
- Become a subject matter expert on Guardant products and data, oncology, and clinical trials.
- Stay current with scientific literature, conferences, and relevant fields.
- Develop marketing messages and collateral for external and internal stakeholders.
Qualifications:
- Typically 8+ years of related experience, or 6 years + Master's degree, or 3 years + PhD, or PharmD/MD.
- Clinical expertise in oncology or genomics is highly desirable.
- Experience working with experts in academic medical centers and/or biopharma is desirable.
- Experience in clinical research, design, or publication is desirable.
- Expertise in genomic biomarker testing (IHC, DNA/RNA, FISH, NGS, digital PCR).
- Advanced knowledge of biotechnology, diagnostics, and pharmaceutical industry.
- Proficiency in Microsoft Office software (PowerPoint, Excel, Word).
- Ability to work independently, remotely, and collaboratively.
- Strong problem-solving, time management, oral presentation, and writing skills.
- Knowledge of genomic LDT, CLIA-88, CAP, Sunshine Act, and FDA regulated diagnostic tests.
- Excellent interpersonal and communication skills.