Two Chicks With A Side Hustle

Our Company

Cerebral is a one-stop-shop for high-quality mental health care.

Since launching in January 2020, we have gone from 5 people in an off-brand WeWork to over 2,000 team members across the United States working hand in hand to transform access to high-quality mental health care at scale. Our team will not stop building, growing, and iterating until everyone, everywhere can access high-quality mental health care without the high cost, wait times, and stigma.

We recently became the fastest mental health company ever to unicorn status, having raised over $162 million and achieved a valuation above $1.2 billion. Cerebral’s investors include Silver Lake, Access Industries, Bill Ackman, Chris Burch, WestCap, and Oak HC/FT.

It is just the beginning for Cerebral, and we need your help as we transform access to high-quality mental health care in the United States and beyond.


Finding the right antidepressant medication can often be a difficult and frustrating process of trial and error. As part of our mission to improve access to high-quality, long-term mental health care, Cerebral is working to expand to provide clients access to the newest, cutting-edge antidepressant treatments through clinical trials.

We are looking for a clinical research coordinator to help clients navigate cutting-edge clinical trials. We need highly organized and responsible individuals to help us closely monitor study participants and schedule both clinical study visits. Attention to detail and adaptability is a must. This role would be an opportunity for a high-performing and motivated individual to kick-start their career at Cerebral via a clinical trial that will be high visibility to Cerebral leadership and external partners.

Please note: This will be a ~six-month, salaried FTE position. Opportunities would exist to extend employment following the successful completion of the clinical trial.

Job Duties:

  • Follow clearly defined research protocol consisting of remote visits over the course of 6-months
  • Participate in training with our sponsor to learn specific procedures, assessments, and devices used in the study
  • Schedule study visit appointments with participants
  • Data collection and entry
  • Serve as point of contact for participant questions and triage appropriately according to the study protocol
  • Complete study-specific training and responsibilities


  • You are a strong verbal and written communicator
  • You enjoy fast-paced and ever-changing work environments
  • You are highly organized and detail-oriented
  • You love working hard, and enjoy having a multi-dimensional role
  • You bring empathy, patience, and grit to all of your interpersonal interactions.
  • You are proficient in using a computer and have the ability to learn how to use new computer programs quickly