Certified Case Manager (CCM), Certified Alcohol and Drug Counselor (CADC), or Mental Health First Aid. Resource Referral and Coordination : Connect clients with essential resources, such as emergency shelter, food, healthcare, mental health services, substance abuse treatment, and employment support.

The Senior Scientist I, Pilot Lab Operations will be responsible for leading the pilot lab operations including GLP biologics drug substance manufacturing, process transfer, pilot lab facility and equipment readiness, manufacturing operation scheduling, planning, preparation and execution.

Ph. D. in Immunology or Neuroscience with over 20 years in academia or in the biotech/pharmaceutical industry, including 10+ years in drug discovery. Set strategy for our research areas and maintain strategic focus across multiple complex drug discovery programs, prioritize resource allocation, and drive decisions consistent with company goals.

Our 2022 Annual Security Report also outlines various campus safety and security policies, such as those concerning crime reporting, prevention and response to sexual and gender violence, alcohol and drug use, crime prevention, emergency response and evacuation procedures, and other matters.

Requires a minimal of 5+ years in genomics, synthetic biology, or drug development. Expertise in the application and use of NGS and/or synthetic biology will be highly valued. This individual will be responsible for driving product and application-based messaging across Twist’s business units, including core initiatives toward cancer research, drug discovery, and human genetics.

Contribute to or lead the design and interpretation of tissue-based studies investigatingaspects such as target biology, drug MOA, target pathway activation, pharmacodynamiceffects, biomarker prevalence, or drug distribution.

This well known and well established agency provides psychiatry, medication management, outpatient substance use treatment, case management, supportive housing, LGBTQ youth and youth care.

The VP of Drug Safety & Pharmacovigilance will interface with vendors, external experts, business partners, investigators, and government agencies. The VP of Drug Safety and Pharmacovigilance will provide the leadership and management for the infrastructure of the Drug Safety and Pharmacovigilance department across both clinical development and commercial products for the company.

Williams Lea is a drug-free workplace and performs pre-employment substance abuse testing. Skilled in the use of mail, phone, email, digital reprographics and mail equipment. Use equipment and supplies in a cost-efficient manner.

The Associate Director of Drug Safety Operations reports to the Head of Drug Safety Operations and will work collaboratively within the Drug Safety department, cross-functionally with other departments, and with partner companies to achieve department and company goals.

Understanding of standard drug development process, defining in vivo pharmacology, assessing PKPD and deriving margins to provide clinical starting doses. Conceptualize and design strategies for drug discovery using insitro's platforms from hit to lead using industry standard preclinical pharmacology models and standard drug development models by applying insights exposed by insitro's unique target discovery credentialization.

The successful candidate also will have the opportunity to help investigate new technologies related to drug delivery, pharmaceutics, and other areas relevant to Merck’s drug discovery/development programs.

Lead Drug Substance process development teams responsible for early and late-stage manufacturing processes. This individual will be responsible for leading multiple teams developing early and late-stage CAR-T drug substance processes across Allogene’s pipeline.

We are seeking a Senior/Principal Scientist - Computational Chemist to drive drug design with state-of-the-art machine learning and physics based methods in a fast-based and early-stage, future-looking company that is championing an in silico -driven drug discovery process.

Completes drug safety monitoring and tracking in a timely, thorough and accurate manner in accordance with pharmacovigilance (PV) and related standards, regulations and Genentech/Roche Standard Operating Procedures(SOPs.