We are a VC-funded, SF-based (East Bay)
started by an MIT professor. We are post-revenue and poised to enter phase 3 clinical trials for treating neurodegenerative disorders, such as Alzheimer’s Disease, based on our positive phase 2 trial results.
We are looking for a Clinical Scientist
to work closely with the Director of Scientific Operations and the Chief Scientific Officer. The primary focus immediately will be in participating in the setup and execution of several human clinical studies and writing reports for regulatory agencies.
The position provides a phenomenal opportunity for a talented individual who seeks exposure and participation across all dimensions of a very well-positioned pharmaceutical company’s growth.
Provide Scientific Support for the setup and execution of single and multi-site human clinical in neurological and psychological disorders.
Protocol design and writing
Clinical trial regulatory document writing
Provide scientific support to sites and Clin Ops Team - screening and outcome measure training, database review of
for data and query review.
Participate in Clinical Trial Data analysis
Write regulatory documents such as INDs, study reports, and FDA correspondences
Other roles as may be relevant to support the Company’s strategy
PhD in Biomedical Field, preferably in Neuroscience or Clinical Psychology
2-5 years of pharmaceutical industry experience
Experience in neurology clinical trial design, setup, and closeout
Experience with clinical trials in neurodegenerative disease such as Alzheimer’s Disease preferred
Familiar with cognitive and neuropsychiatric clinical trial outcome measures
Clinical Trial statistical principles and data analysis
Familiar with SPSS or similar statistical package program for analyzing human clinical trial data preferred
Experience writing regulatory documents such as IND preferred
Working Hours, Start Date and Location-
This position is full-time with an immediate start date, and will be located in Walnut Creek, CA.
Compensation commensurate on experience and qualifications.
Your CV should contain a list of clinical and regulatory experience and list of scientific publications.
Job Type: Full-time
Clinical Research: 2 years