The Clinical Project Manager will be responsible for the management of clinical studies and the driver of the client relationship. The CPM will have significant influence on project success and maintain executive level relationship with sponsor clients. Overall responsibility of project deliverables.

Provide technical expertise for critical starting materials, drug substance, and/or drug product manufacturing over the life cycle of the products in the Ultragenyx biologics portfolio from development through commercialization. Serve as external manufacturing relationship manager at the respective contract manufacturing organizations (CMOs) and represent manufacturing as part of cross-functional Ultragenyx CMC teams.

The Director/Senior Director of Commercial Learning and Development provides strategic leadership to the Commercial Training function to ensure maximum effectiveness, responsible for the overall creation and delivery of customized training solutions across our entire commercial organization.

Support drug safety and risk management activities across Orca Bio's clinical programs including signal detection, evaluation and management. Assist in the development of risk management strategy and activities for programs, including providing content for RMPs and preparing responses for regulatory authority safety requests. Support safety in clinical trials with review of protocols. Lead the planning, writing and review of periodic safety reports.

Lead, motivate, and support the pharmacy team to dispense prescriptions in a mail-order pharmacy environment to patients, overseeing the pharmacist team (including Pharmacists and Pharmacists Techs), including hiring, scheduling, and day-to-day operational task oversight to promote a safe, efficient, and impactful pharmacy team.

Recursion is seeking a contract Clinical Scientist to oversee all clinical aspects of a Phase I clinical trial, including planning and authoring clinical deliverables, routine medical monitoring, site interaction, and presentations. You will play a role ensuring study protocols are executed appropriately and that the study data is both appropriate and pristine, interacting cross-functionally with multiple disciplines supporting the Study Team.

Leads and drives program oversight in conjunction with Clinical Development and Project Management (PM) and across other functional areas for an indication’s life cycle. Partners with Clinical Development to define overall strategy toward achieving/exceeding program specific corporate targets, identifying and mitigating potential issues, and ensuring budget and timeline compliance. Serves as an escalation point and resolution resource for operational issues.

The MSL/Sr MSL role will represent the real time voice of KOL/HCP input related product development opportunities and scientific exchange on pipeline and commercial products. The candidate will leverage scientific acumen to educate on scientifically complex concepts and products and will have a strategic and innovative style combined with a flexible, hands-on nature that works with a high sense of urgency.

ultra focused – Work together to fearlessly uncover new possibilities. We are seeking a highly motivated and experienced individual to lead formulation and process development for Ultragenyx's small molecule and antisense oligonucleotide drug products. This position will report to the Senior Director of Process Development, and represent drug product development function in CMC development teams to enable successful regulatory filings of new products.