Medical Affairs Research Manager

🕒 il y a 1 mois

🏄 California – Distant

info

💵 $164 900 - $226 750 / an

⏰ Temps Plein

🟠 Senior

🔴 Expert

👔 Manager

🦅 Parrain de Visa H1B

info

🗣️🇺🇸🇬🇧 Anglais requis

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Logo of Guardant Health

Guardant Health

1001 - 5000 employés

Fondée en 2012

🧬 Biotechnologie

⚕️ Assurance santé

💊 Pharmaceutique

Biotechnology • Healthcare Insurance • Pharmaceuticals

Guardant Health est une entreprise de cancérologie de précision spécialisée dans l'utilisation de tests sanguins pour révolutionner le traitement du cancer. Leurs tests innovants fournissent des informations essentielles qui aident à informer les décisions thérapeutiques pour les patients à tous les stades du cancer. En tirant parti de la technologie avancée et des données, Guardant Health vise à améliorer les résultats cliniques et à renforcer l'expérience globale des patients dans la lutte contre le cancer.

Description

• Establish and maintain relationships with top research and clinical experts to identify and pursue opportunities for research collaboration to address unmet medical needs with GH products. • Collaborate with MSL team to address inbound research requests from Field Medical partners to promote deeper understanding of Guardant research practices and strategies. • Consult with Clinical Development to identify clinical unmet needs, evidence gaps and advance evidence-generating studies to support development, commercial launch, reimbursement, and guideline adoption of the Guardant Oncology products. • Champion ISTs through protocol review committee and discussions with research collaborators to advance the research proposals. • Leverage scientific, clinical, and/or technical expertise to influence top key opinion leaders biomarker implementation for their clinical trials and interpretation of Guardant Research Use Only (RUO) and Investigative Use Only (IUO) data returned. • Advance research with Guardant datasets alongside collaborators and champion effective scientific writing for effective data submissions to peer-reviewed. • Provide strategic review and proposed edits for collaborative abstracts, posters, presentations and manuscripts when applicable. • Serve as advocate for scientifically and clinically sound applications of precision oncology assays for clinical trials, oncology research and future clinical care, in alignment with medical strategic plans. • Serve as GH research manager for key academic institutions championing research engagements across the institutions and collaborating with other field teams to support research strategy and engagements. • Review and/or provide input on accurate and up-to-date scientific and medical content, including late-stage treatment landscapes for application/cancer type/s accountable for, for internal and external audiences. • Identify and gather areas of unmet medical need and act as a champion for clinical and research experts, internally elevating feedback and voice of customers. • Maintain awareness of related publications across platforms and generates up-to-date scientific and medical content for applications/cancer type/s accountable for in collaboration with Clinical Development, Medical Enablement and/or Oncology Marketing. • Maintain understanding of competitive landscape and trends in oncology precision medicine. • Lead and/or collaborate with regional cross-functional field team to align on account research priorities and strategy. • Inform and liaise to cross-functional efforts within US Medical Affairs and/or across Guardant teams.

🎯 Exigences

• Typically requires a university degree and typically 8 years of related experience; 6 years and a Master’s degree; 3 years and a PhD; or PharmD/MD. • Clinical expertise or related experience in oncology and/or genomics is highly desirable. • Experience working with experts at academic medical centers and/or biopharma companies to build consensus around new products and/or services highly desirable. • Experience conducting and/or publishing clinical research highly desirable. • Proven experience generating data from a Clinical Development or Research Plan for novel clinical products with KOLs strongly desired. • Expertise in genomic biomarker testing technologies, including IHC, DNA/RNA, FISH, NGS (particularly plasma NGS/liquid biopsy), and digital PCR. • Applies advanced knowledge of the biotechnology, diagnostics and pharmaceutical industry. • Ability to apply advanced knowledge of company product specifications. • Intermediate-to-advanced knowledge of the following computer software programs: Microsoft Office: PowerPoint, Excel, and Word. • Ability to work independently and remotely while maintaining a strong teamwork ethic.

🏖️ Avantages

• Guardant Health is committed to providing reasonable accommodations in our hiring processes for candidates with disabilities, long-term conditions, mental health conditions, or sincerely held religious beliefs.

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