The Senior Bid Coordinator will have budget oversight of small bids and may lead other bid coordinators. Job Summary: Senior Bid Coordinators perform tasks that marshal bid and proposal activities through stages and ensure that administratively they comply with all requirements of the Capture, Bid, and Proposal process.

Prometheus Biosciences, Inc. (Nasdaq: RXDX), is a clinical-stage biotechnology company pioneering a precision medicine approach for the discovery, development and commercialization of novel therapeutic and companion diagnostic products for the treatment of immune-mediated diseases.

The USC Keck School of Medicine - Alzheimer Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic institute comprised of an expert panel of scientific collaborators, committed to advancing the development of new treatments for Alzheimer’s Disease (AD) through innovative clinical trials.

10+ years with pharmaceutical/life science companies with strong understanding of preclinical, clinical, regulatory, drug safety, quality assurance, and FDA requirements. Experience supporting scientific teams for their IT infrastructure, including with Benchling cloud-based biotechnology R&D platform or similar software.

Our team has a proven track record of drug discovery and development, having played pivotal roles in the discovery of multiple clinical-stage compounds as well as approved drug for the treatment of cancer and immune-mediated inflammatory diseases.

This position will also interface closely with the Clinical, Research, and Business Development functions as well as Executive Management to support corporate objectives, including aspects of clinical trial design and execution, management of clinical advisory board meetings, scientific disclosure planning, development and review of educational materials, and assessment of potential new indications and in-licensing opportunities to advance and expand the Company's pipeline.

Senior Clinical Research Associate I, FSPUSA - West Coast OnoclogyOncologyAs a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries.

Acadia is seeking an accomplished neuroscience research and development expert with leadership experience in translational medicine and early-stage clinical drug development strategy and tactics.

Certification is required in some areasPrefer 3-4 years of experience in the medical device, biotechnology, and tissue segments of the healthcare industryPrevious experience in high-growth organizations and developing relationships that fueled the organization's growthSKILLS/COMPETENCIES:Excellent oral, written, and interpersonal communication skillsProficient in the Microsoft Office suite (i.e. Excel, PowerPoints, etc.

5+ years of industry experience in small molecule drug discovery with a clear understanding of program strategy, therapeutic hypothesis, assay relevance and clinical translation, and the importance of physical-chemical properties as it relates to enabling late-stage in vivo studies and clinical dosing.

To advance the FALCON platform toward and into clinical development, DTx has raised more than $100M in combined investment from several of the worlds leading healthcare investors including RA Capital Management and Access Biotechnology, pharmaceutical companies such as Eli Lilly and Company, the National Institute of Health (NIH), and research foundations such as the CMT Research Foundation (CMTRF.

Media sales research software and data experience (Nielsen, Scarborough, CMR, Wide Orbit)•Self-starter with the ability to work under pressure, complete multiple tasks, meet deadlines, and adapt to changing priorities.

Collaborate with cross-functional teams, including clinical development, regulatory affairs, statistics, data management, and clinical operations, to ensure the timely and accurate delivery of documents.

This is a unique opportunity to work with a proven and well-funded drug discovery and development team in a small company environment in the heart of San Diego's biotechnology community.

3 - 6 years of pharmaceutical industry experience – prefer knowledge of cell and gene therapy and / or biotechnology / biologics products, including multi-disciplinary experience, 2-4+ years of CMC regulatory strategy (cell therapy experience preferred.