Associate Director, Real World Evidence – Pharma Co Experience Required

🕒 vor 1 Monat

🌵 Arizona, District of Columbia, +3 weitere Bundesländer – Remote

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

💵 $114.000 - $210.900 / Jahr

⏰ Vollzeit

🟠 Senior

👔 Direktor

🦅 H1B-Visum-Sponsor

Dieses Unternehmen hat in der Vergangenheit H1B-Visa gesponsert.

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Syneos Health

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10.000+ Mitarbeiter

🧬 Biotechnologie

💊 Pharmazie

⚕️ Krankenversicherung

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health ist eine führende, vollständig integrierte biopharmazeutische Lösungsorganisation, die darauf ausgelegt ist, den Erfolg ihrer Kunden zu beschleunigen. Sie übersetzen einzigartige klinische, medizinische und kommerzielle Erkenntnisse in Ergebnisse, um den Anforderungen des modernen Marktes gerecht zu werden. Durch die Nutzung fortschrittlicher Technologien und Erkenntnisse arbeitet Syneos Health mit Kunden zusammen, um die Bereitstellung wichtiger Therapien für Patienten weltweit zu beschleunigen, und bietet Dienstleistungen, die das gesamte Spektrum von der klinischen Entwicklung bis zur Kommerzialisierung abdecken.

Beschreibung

• 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

🎯 Anforderungen

• 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

🏖️ Vorteile

• 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