Associate Director, Real World Evidence – Pharma Co Experience Required

🕒 Maio 9

🌵 Arizona, District of Columbia, +3 estados a mais – Remoto

🌵 Arizona – Remote 🏛️ District of Columbia – Remote 🦞 Maine – Remote 🏈 Ohio – Remote ⚓ Rhode Island – Remote

💵 $114.000 - $210.900 / ano

⏰ Tempo Integral

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👔 Diretor

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Syneos Health

SiteLinkedInTodas as Vagas

10.000+ funcionários

🧬 Biotecnologia

💊 Farmacêutico

⚕️ Seguro de Saúde

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health é uma organização líder, totalmente integrada, de soluções biofarmacêuticas, criada para acelerar o sucesso dos clientes. A empresa transforma insights exclusivos clínicos, de Assuntos Médicos (Medical Affairs) e comerciais em resultados para responder às realidades modernas do mercado. Ao utilizar tecnologias avançadas e insights, a Syneos Health colabora com os clientes para acelerar a entrega de terapias importantes a pacientes no mundo todo, oferecendo serviços que abrangem todo o espectro do clínico ao comercial.

Descrição

• This role is open to US employees with no sponsorship needs • Collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals • Act with a drug development mindset, applying years of experience and deep expertise to understand customer needs • Construct cohorts using RWD sources and evaluate key variables • Conduct analyses for descriptive and comparative research using RWD • Coauthor abstracts and manuscripts for external dissemination of results

🎯 Requisitos

• PharmaCo experience required • Developed and executed under Scientific Oversight study protocols, analysis plans, and study reports to answer research questions of priority to RWE • Designed and managed epidemiological, biomarker and/or data science projects • Planned, designed, and conducted analyses for internal and external decision making (e.g., responses to regulatory authorities, rapid analyses of safety queries) • Supported the identification of fit-for-purpose data for the timely execution of the RWE strategy • Constructed cohorts using RWD sources (e.g., claims, EHR) and evaluate key variables, including diagnosis and procedures codes, and plan validation studies as needed • Conducted analyses for descriptive and comparative research using RWD (examples include claims, EHR, PRO/COA, registry data) for methodologic research questions • Contributed to the communication of observational research results and methods, including development of pertinent sections of regulatory documents, reports, publications, white papers • Supported the effective communication of study/analysis results to support internal and external decisions • Coauthored abstracts and manuscripts for external dissemination of methodologic study results • Contributed to the development of processes and training aimed at increasing the efficiency, quality, and impact of functional activities • Technical Expertise o Observational research methods (both Primary and Secondary Data Collection), deep knowledge of biostatistics and analysis methods, understanding of regulatory processes • Project Implementation o Protocol writing, SAP, manuscript and abstract writing

🏖️ Benefícios

• company car or car allowance • Health benefits to include Medical, Dental and Vision • Company match 401k • eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • flexible paid time off (PTO) and sick time