TEMP - Sr. Specialist, Medical Communications

Who We Are:

At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs.

What We Do:

Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis* and uterine fibroids,* as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X and Facebook. (*in collaboration with AbbVie)

About the Role:

Responsible for coordinating publications, building and managing library services and completing other medical affairs projects as assigned. The role may include, providing product information to health care professionals and patients. Responding to questions regarding products in a timely manner. Assist with the creation and maintenance of the product knowledge database used in responding to medical questions related to company products. Work interactively with Clinical Research, Sales and Marketing, Regulatory, and Research personnel to obtain necessary information and to inform other personnel of new issues which may arise. Assist with the receipt, processing, and dissemination of safety information and with the preparation of reports for governmental regulatory agencies.

_

Your Contributions (include, but are not limited to):

• Utilize therapeutic area (TA) expertise to develop and communicate scientific platforms through insightful contributions to the publication plan and other Medical Communication deliverables

• Research and respond to Level 2 Medical Information (MI) request escalations using various search and retrieval techniques to develop a medical/scientific response that is accurate, fair balanced, and delivered in a timely manner

• Serve as an expert Medical resource to the MI Call Center vendor and internal stakeholders

• Support the partnership with the publications agency in managing the tactical execution of the publication plan

• Help manage author/ key opinion leader (KOL) relationships and work with author teams to develop publications

• Plan and help build the infrastructure to support the literature requirements of a mid-size biopharmaceutical company including Regulatory filings, Research and Development summary documents, and Business Development due diligence

• Identify, procure and interpret the findings of emerging scientific literature relevant to the Co