The Senior Medical Science Liaison I is a field based scientific expert that strategically supports the research and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory. The Senior Medical Science Liaison I is the primary communicator of Abbvie science within a specific geography with healthcare professionals.

Receive and respond to prescription refill requests through various communication channels, including phone, email, fax, and Telephone Encounter. Verify the validity and accuracy of prescription refill requests received, ensuring compliance with regulatory guidelines. Prepare and dispense prescription refills accurately and efficiently, following established organizational protocols and procedures.

As a Quality Assurance Specialist at Dynavax, you will support activities related to Quality Systems including Document Control, Training, Quality Records Management, Supplier Management, Audits, and Quality Event Management (Deviation, CAPA, Change). This position will support the upgrade implementations and maintenance of the electronic Quality Management System (eQMS) used company-wide.

Veeva is seeking system implementation experts to join the Professional Services team and support implementations of our Vault Safety solution. As a key member of our Professional Services team, you will work side-by-side with customers and our senior consultants to implement Vault Safety. You will define and drive business processes and guide our customers throughout the implementation programs.

The Medical Science Liaison is a field based scientific expert who strategically supports the scientific and business objectives of a designated therapeutic area across the product life cycle for a specific geography/territory. The Medical Science Liaison is the primary communicators of AbbVie science within a specific geography with healthcare professionals.

The Clinical Operations Program Director is responsible to connect science and operations to bring clinical studies to life through the execution of one or more clinical research programs. The Clinical Operations Program Director serves as a strategic advocate for pipeline assets and provides operational reality to our scientific experiments via scientific expertise, strategic thinking, a global mindset and innovative solutions to address risks and challenges.

This role is integral to RayzeBio’s mission to be recognized as a trusted partner. The Senior MSL serves as the primary medical resource for the external community, facilitating peer-to-peer discussions and translating science into patient care. They identify disease and product-related medical needs, develop relationships with KOLs and HCPs, and ensure patients have access to clinical trial compounds and marketed products.

Oversee Quality Assurance for on-market products from commercialization through end of life, ensuring compliance with all relevant standards and regulations. Maintain Good Documentation Practices (GDP), including product specifications, formula approvals, and audit documentation. Manage Third-Party Testing, coordinating all ongoing testing activities, ensuring appropriate record retention of results, Certificates of Analysis, and other relevant documentation.

The Sr. Manager, CMC Analytics will help oversee analytical method development for API and drug products and oversee testing from product development through commercialization. This role requires extensive experience with method development for small molecule drug product and API testing, particularly with new chemical entities. The ideal candidate should have experience overseeing development as a group leader or managing outside labs and be able to critically review data for potential trends or issues.

As a Manager, Aggregate Reports Scientist, you will spearhead the end to end management of all aggregate reports, including PSURs, DSURs, PADERs, and local reports. Your expertise will establish you as a subject matter expert within the Pharmacovigilance (PV) Scientist team and across Biogen. Your role is pivotal in driving initiatives for process refinement and ensuring compliance with global PV regulations, enhancing patient safety and product stewardship.