Medical Evidence
vor 5 Monaten
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, but few options.
What We Do:
Neurocrine Biosciences is a neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, endocrine and psychiatric disorders. The company’s diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson’s disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. _*in collaboration with AbbVie_
About the Role:
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Your Contributions (include, but are not limited to):
- Leads the design, development and implementation of multiple projects to using disease(s) or product(s) specific evidence to contribute to clinical strategy, medical evidence publications, value assessment and market access- Conducting observational research, generally using local datasets or large healthcare databases to generate a better understanding of disease and real-world outcomes- Developing and/or reviewing protocols and statistical analysis plans for studies assessing the epidemiology, natural history of disease, burden of illness, treatment patterns, healthcare resource utilization/costs, and (comparative) effectiveness of treatments- Critically reviewing literature and querying real-world data to estimate the incidence and prevalence of disease- Supporting the authoring epidemiology sections of regulatory documents- Collaborating with Medical Affairs and HEOR colleagues and other internal partners to disseminate RWE in compliance with company, industry, and regulatory requirements- Maintaining an up-to-date awareness of guidance documents and communications that may impact RWE strategies and RWE generation- Contributing to the advancement of the field of medical evidence generation, RWE/epidemiology and being recognized as an expert by publishing high-quality research in leading journals, presenting at scientific conferences- Collect and analyze data using targeted and systematic large data methods, including developing data collection criteria, collection tools, performing literature searches, and abstracting relevant data- Develop written materials (reports, manuscripts, presentations) for presenting project results- Participate and effectively communicate in internal cross functional team discussions and in meetings with external stakeholders and clients- Work closely within EAME and global product planning cross functional teams to be responsible for population prevalence and incidence content- Collaborates with internal business partners to meet the evidence needs of external consumers (e.g. Health Technology Assessment bodies (HTA))- Lead on the recruiting of RWE experts for meetings, advisory groups, or panels; contributing to or reviewing proposals; assisting with problem-solving; researching potential solutions, manage vendors- Contributes to the creation of EAME Medical Affairs and global HEOR functional vision and goals- Other duties as assigned
**Requirements**:
- Degree and Master's degree in public health or life sciences and 10+ years of similar experience shown above OR- PhD in Public Health or life sciences and 7+ years of similar experience shown above OR- Excellent presentation and highly proficient computer skills (e.g., Word, Excel, PowerPoint,)- Effective interpersonal skills including the ability to build successful relationships with internal experts/teams and other stakeholders- Strong written communication skills- Expert data analytic skills- Sees broader picture, impact on multiple programs/projects, teams and/or departments- Show leadership skills and lead/mentoring lower level employee and / or indirect teams- Excellent project management skills- Job Specific Knowledge & Qualifications:
- Have used large commercial claims and publicly accessible data sets as the foundation of research- Epidemiology experience- Expert statistical modeling including using tools and programs such as R, SAS, STATA or similar statistical programming- Expert knowledge of Excel- Strong publication/medical writing experience is required- Ability to synthesize, analyze and summarize data, think critically, manage projects, influence others- Ability to work in a team environment, across multiple departments- Ability to synthesize complex clinical and no
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