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 (SAM) is responsible for informing, engaging, and influencing key stakeholders (KSH) at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health products and services.
Essential Duties and Responsibilities
- Establish and maintain relationships with key stakeholders at BioPharma, elevating Guardant Health’s reputation and laying foundation for potential collaborations.
- Engage with pharma key stakeholders in scientific exchange to understand current and future oncology biomarker needs.
- Leverage expertise to influence pharma in oncology biomarker implementation.
- Provide strategic review and proposed edits for pharma partner materials (abstracts, posters, presentations, manuscripts).
- Identify and pursue collaboration opportunities with pharma and biotech companies.
- Assess biopharma pipelines for Guardant engagement and potential research collaboration.
- Serve as internal and external advocate for scientifically sound ctDNA applications.
- Establish expertise on Guardant Health products, data, and oncology settings.
- Stay current in clinical oncology, drug development, genomics, and biomarkers.
- Contribute to the development of accurate marketing messages/collateral.
Qualifications
Typically requires a university degree and 8+ years of related experience. Clinical expertise or related experience in oncology and/or genomics is highly desirable. Experience working with experts, designing/conducting/publishing clinical research, and using various genomic biomarker testing technologies is also highly desirable. Requires advanced knowledge of the biotechnology industry and computer software. Excellent communication, writing, and presentation skills are essential. Working knowledge of genomic LDTs and familiarity with CLIA-88, CAP, Sunshine Act, and FDA-regulated diagnostic tests are desirable.
Compensation
Salary range: $157,800 - $213,030 (US dollars).
Work Environment
- Up to 50% travel is possible.
- Home-based office with extensive computer use.
- Ability to work on multiple tasks and in a fast-paced environment.