The Associate Director, Clinical Operations plays a key role in the execution of clinical trials, ensuring operational excellence and successful delivery. This position involves overseeing the day-to-day management of clinical trials and collaborating with cross-functional teams. The role ensures adherence to the highest standards of quality and compliance, contributing to advancing innovative mental health therapies.

As a Prescription Navigator, you will play a crucial role in ensuring members receive the medications they need through our proprietary savings programs. Responsibilities include answering incoming calls to assist members and third parties with medication and insurance plan inquiries, making outbound calls to resolve medication-related issues, and assisting members in navigating cost savings programs.

Syndax Pharmaceuticals is searching for a Director, Health Economics and Outcomes Research and Real-World Evidence (HEOR &RWE). The Director, HEOR & RWE will be responsible for the execution of HEOR & RWE strategy and evidence generation to support Syndax products. Collaborates with stakeholders across the company.

Oversee medical safety activities and processes for assigned products, ensuring continuous assessment of safety profiles and benefit-risk of investigational and marketed compounds. Provide patient-focused leadership for medical safety, support asset strategies, and strengthen medical and scientific innovation. Timely escalation of safety issues to the Takeda Safety Board Chair is required.

In this contracted role, the Virtual Access & Reimbursement Manager supports access for providers and patients by educating healthcare providers and office staff on access services and reimbursement solutions, executing strategic plans through partnerships with stakeholders, and resolving patient-level reimbursement issues in a compliant manner.

The Specialty Care Field Medical, Director is responsible for providing therapeutic area/product expertise for the designated therapeutic area across a broad range of external medical stakeholders in an assigned territory. Identify and seek medical scientific engagement from priority external medical stakeholder segments in assigned Therapeutic Area. This position requires permanent work authorization in the United States.

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.

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.

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.