Chief Medical Officer – Fertility

This is a fully remote position, open to applicants in New York.

📋 Description

• Take ownership of Evvy’s clinical role in the realm of fertility.

• Guide the design and uphold the scientific integrity of clinical trials.

• Formulate prospective interventional studies, encompassing endpoints, inclusion and exclusion criteria, randomization, power calculations, and comprehensive protocols.

• Maximize the evidence generated within an established budget and timeline.

• Sequence and prioritize the study pipeline effectively.

• Utilize the Fertility Advisory Board and external clinical experts in the study design process.

• Direct the IRB submission strategy and ensure that study designs can withstand medical and research scrutiny.

• Collaborate with the internal data science team and the study execution lead on enrollment, site selection, and operational aspects.

• Serve as Evvy’s senior clinical representative in the fertility and IVF sectors.

• Represent Evvy at significant conferences and interact with key opinion leaders in reproductive medicine.

• Act as an internal co-Principal Investigator alongside an independent external PI.

• Present study findings to the field.

• Develop relationships with IVF clinics, REI doctors, and fertility societies.

• Influence the clinical credibility strategy across providers, payors, professional societies, and guidelines.

• Identify opportunities to enhance patient outcomes through stratifications, treatment protocols, intake flows, and educational initiatives.

• Act as a fertility subject matter expert within Product, Growth, and R&D teams.

• Convert clinical and operational insights into scalable product enhancements.

• Function as a clinical thought partner to the founders and board.

⛳️ Requirements

• Board certification in reproductive endocrinology with a recognized standing in reproductive medicine.

• A current academic appointment or equivalent research status.

• A significant record of peer-reviewed publications.

• Direct experience in designing and conducting clinical studies.

• Experience with prospective and randomized studies is highly preferred.

• Active involvement in pertinent professional organizations such as ASRM.

• Proven ability to design studies that adhere to budgetary and timeline constraints.

• Capacity to prioritize endpoint selection, cohort size, and trial duration while balancing scientific and business perspectives.

• Interest in utilizing the vaginal microbiome to enhance fertility outcomes.

• Capability to operate independently as a credible external voice while collaborating with Evvy.

• Willingness to have Evvy as your sole senior position within a private company.

• Expertise in the vaginal microbiome or innovative diagnostics is advantageous but not mandatory.

• Experience in navigating a diagnostic through payor coverage or into clinical guidelines is beneficial but not required.

🏝️ Benefits

• Competitive salary and equity package.

• Flexible PTO.

• $1K budget for learning and development.

• Health, dental, and vision insurance, along with HSA plans.

• 401(k) plan (both Roth and traditional options).

• Monthly team events.

• Complimentary Evvy membership.

• Paid parental leave.