Job Listings

Qpex Biopharma is seeking a highly motivated Clinical Trial Manager or Senior Clinical Trial Manager to oversee the execution of Phase I-III clinical studies from start-up through close-out. This individual will be a key member of our Clinical Operations team, working closely with internal teams, CROs, and vendors to ensure studies are delivered on time, within budget, and in compliance with GCP and regulatory requirements.

Qpex Biopharma is seeking a highly capable and self-motivated Administrative Assistant or Office Coordinator to join our innovative team in San Diego, California. This on-site role is essential in supporting daily operations, streamlining processes, and fostering teamwork across the organization. The ideal candidate is independent, detail-oriented, and skilled at making sound decisions with minimal supervision. They must also possess excellent communication, written, and multitasking skills, providing critical support to leadership and multiple departments to ensure smooth and efficient office operations.

Qpex Biopharma is seeking an experienced, resourceful, hands-on individual to join our Pharmacology team in the role of Bioanalytical Research Associate/Research Scientist. The position will conduct bioanalytical methods using chromatographic assays of small molecule therapeutics for discovery through clinical stages of R&D. This position will be involved in internal and external nonclinical and clinical bioanalytical projects and ensure high quality bioanalytical data/reports are delivered in accordance with project timelines. This position will report to the Principal Scientist, Bioanalytical and will interact with other team members across the company.

Qpex Biopharma is seeking a Medical Director, Clinical Development to join our dynamic antibiotic development team. In this role, you will play a pivotal part in advancing our efforts to develop novel antibiotics to address antibiotic resistance. The Medical Director is responsible for providing medical direction, management and review of clinical trials and product development. Specific tasks may include design of clinical development program plans, as well as clinical protocol development, medical monitoring of clinical trials, and analysis of study data and preparation of trial reports and related regulatory documents. This individual will have a solid understanding...