Guardant Health

Medical Affairs Research Manager

Guardant Health$164K — $226K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 8 years of experience, 6 years with a Master's, or 3 years with a PhD/PharmD/MD in relevant field.
  • Experience in oncology and/or genomics is a plus.
  • Experience collaborating with experts at academic medical centers and biopharma companies is highly desirable.
  • Proven track record in designing, conducting, and publishing clinical research is required.
  • Strong background in developing clinical data with key opinion leaders (KOLs) is preferred.
  • Advanced knowledge of genomic biomarker testing technologies, including NGS and liquid biopsy, is essential.

Responsibilities

  • Establish relationships with KOLs to enhance scientific exchange and collaboration.
  • Identify collaboration opportunities with KOLs to support strategic clinical data needs.
  • Address research requests from Field Medical partners to improve understanding of research practices.
  • Identify unmet clinical needs and execute studies to support product development and launch.
  • Influence KOLs on biomarker implementation for clinical trials using expert knowledge.
  • Conduct research using Guardant datasets and support scientific writing for peer-reviewed submissions.
  • Review and propose edits for collaborative research publications.

Benefits

  • Home-based office environment with modern technology support.
  • Moderate travel (up to 40%) for KOL meetings and conferences is required.
  • Hybrid work model promoting work-life balance with designated in-office days for collaboration.
  • Opportunities for professional development through collaboration with top KOLs and industry experts.
  • Focus on innovative research in the oncology field with a reputable organization.
Full Job Description

Position Summary:
The Medical Research Manager will engage with top Key Opinion Leaders (KOLs) to inform research strategy, foster research collaboration, and promote scientific excellence. They will manage research proposals from the national Field Medical Team to support data generation and research activities for key applications and/or cancer types aligned with company initiatives across academic and community clinicians.

The Medical Research Manager will partner with multiple internal cross-functional stakeholders (Product, Technology Development and Bioinformatics, Clinical Development, Biostatistics, Managed Care and Reimbursement, Commercial) as well as external collaborators, advisors, and KOLs to identify clinical unmet need and evidence gaps to then lead the execution, and publication of clinical feasibility and validation studies, including those focused on clinical feasibility, clinical validity, and clinical utility. Additionally, the Medical Evidence Manager will perform direct research and develop scientific content for internal and external audiences.

Essential Duties and Responsibilities

  • Establish and maintain relationships with top key opinion leaders for scientific exchange, elevating Guardant’s reputation and laying foundation for potential collaborations.
  • Identify and pursue opportunities for collaboration, with input and oversight by leadership, with top key opinion leaders and their institutions that support Guardant Health strategic clinical data development needs.
  • Collaborate with area lead to address inbound research requests from Field Medical partners to promote deeper understanding of Guardant research practices and strategies
  • Identify clinical unmet needs, evidence gaps and execute evidence-generating studies to support development, commercial launch, reimbursement, and guideline adoption of the Guardant 360 Liquid and Tissue products
  • 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.
  • Conduct 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 internal and external advocate for scientifically and clinically sound applications of ctDNA for clinical trials, oncology research and future clinical care
  • Generates 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
  • Maintains awareness of related publications across platforms and generates up-to-date scientific and medical content for applications/cancer type/s accountable for


Qualifications:

  • 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 designing, conducting, and/or publishing clinical research required
  • Proven experience developing and generating data for novel clinical products with KOLs strongly desired

Technical Skills Required:

  • 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.

Work Environment:

  • Moderate travel required, approximately 3-5 trips per quarter to meet with KOLs/PIs, attend conferences, including specialty society scientific meetings (will require some weekend work), and trips to headquarters. Travel is estimated to be up to 40%.
  • Must be physically able to handle travel in vehicle, plane, or other modes of public transport.
  • Office may be home-based, and involves extensive use of computer and keyboard while in home office.
  • Requires the ability to focus on multiple tasks simultaneously, work in high-paced, high-energy environment and the ability to work independently and remotely while maintaining a strong teamwork ethic.

AI & Digital Fluency

  • Demonstrate curiosity, sound judgment, and the ability to critically evaluate and responsibly leverage AI-enabled tools in accordance with company policies, ethical standards, and regulatory requirements to improve the efficiency, effectiveness, and quality of work.


Hybrid Work Model:This section is applicable to onsite employees who are eligible for hybrid work location as specified by management and related policies.  Guardant has defined days for in-person/onsite collaboration and work-from-home days for individual-focused time. All U.S. employees who live within 50 miles of a Guardant facility will be required to be onsite on Mondays, Tuesdays, and Thursdays. We have found aligning our scheduled in-office days allows our teams to do the best work and creates the focused thinking time our innovative work requires. At Guardant, our work model has created flexibility for better work-life balance while keeping teams connected to advance our science for our patients.

The annualized base salary ranges for the primary location and any additional locations are listed below. This range does not include benefits or, if applicable, bonus, commission, or equity. Each candidate’s compensation offer will be based on multiple factors including, but not limited to, geography, experience, education, job-related skills, job duties, and business need. Primary Location: Remote - Open Position (USA) Primary Location Base Pay Range: $164,900 - $226,750 Other US Location(s) Base Pay Range: $164,900 - $226,750 If the role is performed in Colorado, the pay range for this job is: $164,900 - $226,750


Employee may be required to lift routine office supplies and use office equipment. Majority of the work is performed in a desk/office environment; however, there may be exposure to high noise levels, fumes, and biohazard material in the laboratory environment. Ability to sit for extended periods of time.

About Guardant Health

Guardant Health, Inc. is a precision oncology company that develops and commercializes blood tests for early cancer detection and treatment. The company's flagship product, Guardant360, is a liquid biopsy test that analyzes cancer-related genes in the blood to help doctors make more informed treatment decisions. Guardant Health was founded in 2012 and is headquartered in Redwood City, California. The company has partnerships with several pharmaceutical companies and has received FDA approval for several of its products.
Learn more about Guardant Health
Size
1,373 employees
Market Cap
$2.8 billion
Industry
Net Income
-$253.7 million
Founded
2012
5 Year Trend
+71.4%
Revenue
$286.7 million
NASDAQ

Similar Jobs

More Jobs at Guardant Health

More Pharmaceuticals & Biotech Jobs

Find similar Medical Affairs Research Manager jobs: