Please share what your role is at PicnicHealth.
As the head of patient affairs and advocacy, my role is to guide and empower cross functional stakeholders to effectively integrate the patient perspective and voice into the studies, features, and products that we deliver.
Can you share your background prior to PicnicHealth?
I started my career 20 years ago as a HIV test counselor and college health educator, developing health education and prevention programs for students and community members. It was a great introduction to the dynamics of public health, community engagement, and the political nuances of resourcing a chronically undervalued service. Since then, I’ve had the privilege of serving communities through various roles, from health program consulting for large government contracts to, most recently, a decade in rare disease patient advocacy.
What does your day-to-day at PicnicHealth look like?
On any given day, I’m connecting with patients and advocacy organization leaders about what is happening in their communities and bringing those insights back to our team to enhance our platform and inform research with our partners. I also work with our partners to understand their challenges answering key research questions for new treatments and therapies and problem solve solutions for them. When I’m not on a call, I’m researching the feasibility of engaging new communities or specific patient populations for studies on the PicnicHealth platform, and collaborating with our incredible recruitment and enrollment team to understand the impact we’re having on patients as we roll out new campaigns.
Fun fact: Fun fact about me – I was a choir and musical theater kid from birth and still love to sing as loud as possible (but mostly in my car now, much to the dismay of my seven and nine year old children).