In our passionate pursuit to radically improve health outcomes, we serve humanity when we:

Lead with Science, Anchor in Pragmatism

: We pioneer life-changing science by ensuring quality, transparency, and rigor at all times. We explore thoughtfully, experiment smartly, and deliver impact with conviction.

Build With & For All

: We embrace diverse backgrounds to innovate and achieve together. We are not just building a product - we aim to disrupt the path of cancer for all - no matter geography or socioeconomic class 

Put We over I

: We are a home for high-performing people. Through teamwork, we build collective intelligence. Each of us wins when those we serve and those who serve with us--win. We show up with empathy, humility, and integrity at every step of the journey.

**DELFI has 1-2 designated in-office working days each week for employees who live within within 50 miles of Palo Alto CA or Baltimore MD offices

In the Medical Director/Senior Medical Director (Clinical Development & Medical Affairs) role you will work collaboratively with DELFI clinical development, medical statistics, medical affairs, reimbursement and market access, and externally with clinical experts, guideline organizations, patient advocacy groups, and key opinion leaders to establish understanding of DELFI clinical research and technology. You will also support the generation of product related evidence through review and support of external investigator led studies, and on developing and implementing Real World Evidence generating registries of DELFI technologies in clinical use, focused on enriching the ability of clinicians, payers, and regulatory authorities in the US and abroad. You will play key leadership and participatory roles in DELFI’s own clinical development program including interacting with study sites and collaborating on protocols.

*Medical degree (MD, DO or equivalent) with 5+ years of clinical practice is required for this role*

What you’ll do

• Serve as expert clinical contributor within the company regarding clinical use and enhancements of current and potential DELFI technologies
• Contribute to the protocol, monitoring plan, and CRF development for DELFI clinical trials by working collaboratively with Clinical Operations, Clinical Data Management, Statistical Science, Medical Communications, and Regulatory groups at DELFI. Regularly engage expert advisors on matters of study design and endpoints
• Ensure execution of clinical trials in support of DELFI’s clinical evidence strategy.
• Provide project team training on disease and/or therapeutic areas

What you’ll have accomplished 12 months from now

• Executed on DELFI clinical studies, acting as medical monitor, facilitating execution and data interpretation

• Lead the preparation of clinical study reports for on-going studies, provide medical input for publications and support Regulatory strategy, including submissions

• Provide internal education and clinical insight to help refine DELFI product use applications

• Closely monitored and ensured clinical compliance and high scientific standards in ongoing trials

• Fostered relationships with KOLs in US and internationally for the assessment of DELFI technology, evidence evaluation and clinical guidelines, including relevant clinically focused advocacy organizations

• Supported the launch of at least one investigator initiated study

• Presented at several relevant scientific conferences and medical meetings

• Provided evidentiary structure and helped design and prepare registry of DELFI technology in real world use

• Provided registry guidance for new products

• Required

• Medical degree (MD, DO or equivalent) with 5+ years of clinical practice

• Prior clinical trial implementation experience in Pharma or Medical Devices

• Thorough understanding of medical practice and diagnosis related to pulmonology, cancer care or screening

• Knowledge  of regulatory and GCP elements of clinical trials

• Excellent organization, communication, presentation, critical thinking, and interpersonal skills

• Ability to influence and build and  foster relationships horizontally and vertically across the organization

• Ability to communicate with senior leadership, clinicians, and regulatory authorities.

• Excellent writing and presentation skills required

• Availability for up to 25% business travel

• Preferred

• Prior experience in vitro diagnostic diagnostics development

• An advanced degree in public policy or public health

• Molecular diagnostics, genetics, or related scientific field background

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

This position is not eligible for agency partnership. Resumes and outreach from staffing representatives will be declined.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Total Compensation at DELFI is a combination of salary, bonus, equity, and benefits. Actual compensation packages are based on a wide array of factors unique to each candidate, including but not limited to skillset, years & depth of experience, certifications & relevant education, geography.****