Medical Affairs Research Manager
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.
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.
- 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).
- 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.
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%.
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.
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.
This role is open to remote positions in the USA.