Hello! I’mm the VP for San Francisco and am responsible for the growth of our West Coast offering. As Meet’s longest serving hire I have been part of this journey since 2011. Having built and led successful permanent and contract recruiting teams in our London HQ, I launched our San Francisco business in 2016. From a standing start, we are now successfully partnered with an exciting client base that covers San Francisco, Los Angeles, San Diego and Seattle for both permanent and contract recruiting.
Reporting to the Head of Clinical Supply Chain the Manager, Clinical Supply Chain will ensure that all clinical trials, including multiple global Ph III studies, have timely and adequate supply for administration to patients. The Clinical Supply Chain group is involved in a clinical trial from the early stages of inception to study closure. This role includes demand forecasting, determination of an appropriate presentation to the clinical site and subject, setting production schedules, inventory management at depots and sites, order management and proof of delivery, return or destruction and global distribution logistics including import and export management
Salary $100000 - 120000
Location South San Francisco
My client, a leader in the development of medicines for high unmet medical needs, is seeking a Quality Assurance Manager who will be an integral part of the Compliance group at the South City site. Reporting to the Director of Post-Marketing QA, this position will be assist on promoting a quality mindset at the site, supporting vendor audit oversight and inspection readiness.
Location South San Francisco
Come join a dynamic late-stage small pharmaceutical company in the Bay Area who are looking to expand the Quality group with the addition of a Clinical Quality Associate Director/Director. Based in either the San Bruno office, or Canada, my client is looking for a GCP compliance expert to join a tight- knit team oriented group to oversee all activities related to development and direction of the Global Clinical Quality strategy, objectives, policies and programs pertaining to development and marketing of drug products for a molecule. This company has multiple assets across Ps I- III and their lead product is due to start up Ph III in 2018.
Location San Bruno
A biopharmaceutical startup company focused on delivering innovative women’s health and prostate cancer solutions is looking for a Senior Director of Regulatory Affairs to join their team! In this position, you will have the exciting opportunity to provide leadership for their global regulatory activities. You will be in charge of nonclinical, clinical and CMC regulatory filings and provide strategic as well as operational leadership for the project teams. This is a fantastic opportunity for an established Regulatory Affairs leader looking to make the change to a growing startup company!
Location South San Francisco, CA