MAC Reference Librarian

ABOUT AMGEN

Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today.

ABOUT THE ROLE

The MAC Reference Librarian will be responsible for managing the digital Reference Library and Match Text Library within the Veeva Global PromoMats system, while adhering to internal guidelines, SOPs (Standard Operating Procedures), policies and industry regulations.

Roles & Responsibilities:

• Manage Reference and Match Text Libraries for multiple US MAC Teams
• Adding new Match Text records and adjusting existing records.
• Manage Amgen Label Reference documents in Veeva
• Organize annual reviews
• Supports Global Initiative/Other MAC related projects.
• Expert in MAC Reference Requirements and Veeva Reference & Annotation (R&A) technology.
• Performs Quality Check on all References uploaded into the Reference Library to ensure aligned to R&A requirements
• Builds & maintains strong relationships with project Sponsors (owners), Reviewers, agencies, and other MAC Cross functional partners while also providing training on Reference Library and Linking requirements & identify Reference QC issues
• Collaborates with Material Compliance Managers (MCM) to understand BU/Product business priorities and elevate process issues that arise
• Collaborates with MCA to identify and correct Reference QC issues
• Partners with SciComm to update Links to Reference Anchors in MAC materials
• Manage the MAC Reference Library email Inbox.
• Create and manage associated work instructions.
• Facilitate weekly Reference Library Office Hours
• Reports to the Director of Material Compliance in Regulatory Affairs

Required Knowledge and Skills:

• Ability to foster collaboration, work effectively on cross-functional teams, and consistently deliver on-time.
• Strong oral and written communication skills; strong interpersonal skills; demonstrated time management and decision-making skills.
• Critical thinking and problem-solving skills
• Quick learner, proactive, takes initiative.
• Distinguishes proper balance between strategic and tactical thinking.
• Strong experience with Project Management tools, methodologies, and practices
• Proven ability to manage in a highly fluid, interactive, matrix environment.
• Authoritative command of complexity and ambiguity, ability to see the big picture, ability to collect, digest and assemble information to enable relevant business analysis and influence decision-making.
• Identify continuous process and system improvements to save time and cost to Amgen.

Preferred Knowledge and Skills:

• An understanding of the pharmaceutical commercialization process and knowledge of the legal and regulatory guidelines affecting promotion of prescription products
• Project management experience in the Pharmaceutical, Biotechnology or other Healthcare-related field, or other regulated industries
• Experience with Microsoft Office 365 (e. g. Word, Excel, Outlook, and PowerPoint), Adobe products (e. g. Adobe Photoshop, Illustrator, and Acrobat Pro), and Veeva PromoMats
• Experience managing medical reference support for marketing materials that are produced at high volumes.
• Experience managing digital library and medical references.

Basic Education and Experience:

Bachelor s degree and 6 years of related experience

OR

Associate s degree and 10 years of related experience

Preferred Education and Experience:

• Bachelor s degree and 6 years of related experience
• Experience working in a Global Regulatory Affairs organization

AIN working hours for this position:

This position supports the Regulatory Promotion and Material Compliance activities serving Amgen s US Business Operations and thus the AIN working hours will need to be flexible with occasional overnight work time when needed to support product launches and new indications.

EQUAL OPPORTUNITY STATEMENT