Clinical Research Coordinator, Cerebral Care

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.

Opportunity

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

Requirements

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

APPLY HERE