ABOUT UNLEARN

Recent progress in artificial intelligence coupled with a growing resource of longitudinal patient data from historical clinical trials and real world sources provides an unprecedented opportunity to transform clinical trials and speed the development of new medicines.  

Unlearn is a science-first company that has invented the first machine learning platform for creating Digital Twins of patients in clinical trials — comprehensive simulations that answer “what would likely happen to this patient if he/she were randomized to the control group?”.

Using information from Digital Twins to estimate treatment effects reduces required sample sizes, increase statistical power, and provides patient-level treatment response information. 

It's about increasing confidence in trial results. 

It's about bringing new medicines to patients faster.

It's about time.

YOUR ROLE AT UNLEARN:

Unlearn is looking for an experienced, strategic Clinical Affairs professional to join the team. She/he shares the excitement about our transformative solution. She/he is an innovative clinician helping to design and execute clinical studies to demonstrate the value of Digital Twins,  and to enable their widespread use to bring medicines to patients faster. She/he will partner with internal and external experts to shape Unlearn's offering through collaborations with leading pharma scientists and drug developers. The role reports directly to CCO. 

Day-to-day work will include:

• Contribute clinical insights and subject matter expertise into the product development process including clinical trial design, analysis, and interpretation.
• Generate a scientific publication strategy to communicate the clinical evidence that supports the use of the digital twins and ICAs and educate various audiences.
• Develop relationships with key clinicians/institutions and lead research collaborations.
• Provide scientific and clinical input into customer communications, marketing/sales materials.
• Collaborate with the Commercial organization on customer interactions and scientific presentations. 
• Work with Regulatory to develop submission materials for filings and participate in interactions with regulatory bodies.

Qualifications/Requirements:

• PhD or MD degree 
• 6+ years of relevant experience within pharma/biotech or medicine.
• Experience in neurologic diseases preferred but not required
• Drug development expertise including clinical trial design and knowledge of statistical methods. 
• Experience in establishing strong, collaborative working relationships with internal stakeholder functions and external customers 
• Ability to learn quickly, communicate effectively, and present complex new ideas with clarity and simplicity
• Strong initiative, creativity, sense of urgency, and time management skills

COMPENSATION/BENEFITS

Unlearn offers compensation commensurate with experience as well as a competitive benefits package, including:

• Generous equity participation.
• Unlimited PTO plus company holidays.
• Annual company-wide shutdown between Christmas and New Years holidays.
• Professional development budget to attend conferences or other events.
• 401k plan with generous matching.
• Company-subsidized medical, dental, & vision insurance plans.
• Commuter benefits plan.
• Paid Parental Leave

Unlearn is not currently offering visa sponsorships for any position. Please only apply if authorized to work in the U.S.