Truvian is looking for a Director/Sr
Director, Clinical Studies, as we enter our next evolution phase
In this role, you will develop the strategic plan for clinical development studies and clinical
trials to achieve specific study objectives in alignment with business goals
This is also a hands-on position where you will oversee all stages of clinical study execution,
from initial planning to study completion, in compliance with applicable regulatory standards
and Good Clinical Practice (GCP)
You will work with an interdisciplinary team of internal and external stakeholders, including
regulatory, product development, marketing, and scientific affairs, to ensure the studies are
designed appropriately and will deliver high-quality data to support evidence-based product
claims
This role will report to the Sr
Director of Clinical Development and Scientific Affairs (CDSA).
HERE‘S WHY YOU‘LL LOVE THIS JOB:
* You will be setting the strategy and managing clinical studies execution to generate data
that substantiate the performance of Truvian‘s breakthrough blood testing technology
* You‘ll work with a rock-star team of people who are passionate about the work they do
and our ability to disrupt healthcare with our innovative products
* You‘ll be a key player on a team responsible for the company‘s growth and product
launch
* You‘ll thrive in a fast-paced and dynamic environment where you can implement fresh
ideas new processes and make things happen quickly without a bunch of red tape
* You‘ll have great perks such as Generous Benefits (Medical/Dental/Vision/EAP/Paid Life
Insurance/LTD/401K), paid parental leave, flexible PTO, Kombucha and cold brew on tap, craft
coffee, a variety of healthy snacks, on-site gym and virtual classes, and a farm to table
onsite restaurant including a 30% discount
WHAT YOU WILL DO:
Broadly, this role is responsible for delivering Truvian‘s diagnostic products to
diverse, global end markets. |