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Manager, Rare Disease RWE Scientist
Company: Pfizer
Location: New York City, NY
Employment Type: Full Time
Date Posted: 04/10/2021
Expire Date: 06/07/2021
Job Categories: Biotechnology and Pharmaceutical, Computers, Software, Consulting Services, Finance/Economics, Government and Policy, Healthcare, Other, Healthcare, Practitioner and Technician, Information Technology, Legal, Manufacturing and Production, Science, Executive Management, Franchising, Research & Development, Medical
Job Description
Manager, Rare Disease RWE Scientist

The Real World Evidence (RWE) Center of Excellence (CoE) is a rapidly expanding group that provides integrated, end-to-end RWE optimization, education, communication, and maximization of data partnerships' value within therapeutic areas (TAs) to meet both core and innovative Development, Regulatory and Commercial needs to support breakthroughs to change patients' lives.

The Rare Disease TA is responsible for creating and commercializing therapies for rare disorders. Cross-functional pipeline and asset teams create and deliver biologic medicines, small molecules and exploratory gene therapies.

Within the Global RWE CoE, a dedicated team of RWE Scientists reporting to the Rare Disease RWE Lead will support the TA. Leveraging their understanding of how RWE can support the entire lifecycle, the Rare Disease RWE Scientist Manager will deliver timely real world insights (RWI) and RWE in collaboration with cross-functional teams, provide guidance on appropriate sources of real world data and methods, and will create easy-to-understand summary reports. Where external data sources or services are required, they will help oversee / consult for any external RWE studies. For both approaches, the RWE Scientist Manager will ensure the development and application of consistent business rules and standards, versioning rules as care pathways evolve.

The Rare Disease RWE Scientist Manager will play a key role in delivering RWE projects and support the development of RD RWE strategy to keep up with the evolving regulatory and payer environment.


+ Create real-world insights for feasibility assessments, go/no-go decisions, co-design and create dashboards to inform cross-functional teams' hypothesis generation, generate timely and detailed insights

+ Coordinates cross-functional teams to create high quality RWE from rigorously designed protocols

+ Partner with and coordinate the Rare Disease and Strategic Partnerships and Operations RWE Leads, other RWE Scientists, RWE Biostatistics, Digital RWD and other colleagues as needed to collaboratively develop high quality methods, approaches, protocols and designs

+ Generate RWE through collaborations with the pipeline / asset teams (eg, Early Clinical Development pipeline teams, Global Product Development franchise / asset teams, BU Medical affairs, HEOR, Commercial), RWE Biostatistics and other functions

+ Proactively identify opportunities to automate and create efficiencies, harmonize rules with other analysis teams

+ Lead vendor due diligence for potential partnerships or new sources of data / technology as directed

+ Document all requests and track progress toward project completion, other metrics and business goals


+ 2+ (with a master's degree) to 3+ (Bachelor's degree) years' experience in the pharmaceutical industry/consulting

+ Proven successful track record of scientific analysis of real- world data for scientific, business, quality or other purposes

+ Knowledge of Electronic Health Records, medical and pharmacy claims, patient registries, patient participating research networks and other real-world data sources

+ Ability to critically evaluate analytic results against the literature, subject matter expert feedback or other reliable sources to ensure biological and medical credibility in alignment with cross-functional team strategy / priorities

+ Two or more years of experience in communicating in verbal and written form with all levels of personnel with diverse backgrounds, and able to create and deliver clear presentations to teams

+ Ability to work under pressure with a high level of autonomy and internal motivation and adapting rapidly within evolving digital environment

+ Experience with protocol development and execution for non-interventional studies using a variety of analytical techniques applied to various databases

+ Two or more years of hands-on experience of query and analytic languages and technologies (eg, SQL, R, SAS, IHD, Aetion) and of relevant biological and medical data standards (eg, HGNC / Entrez, ICD, CPT)

+ Ability to rapidly learn new domains to understand the latest scientific or medical findings and incorporate them into projects as appropriate; to interpret data dictionaries and other technical documentation


+ The ideal candidate will have a Master's degree with 3+ years/PhD with 1+ years in RWE analytics, Economics, Bioinformatics, Epidemiology, Biostatistics, Other Biological Science fields with a substantial quantitative and computational component, other related fields or commensurate professional experience

+ 2+ years of experience working in real world data analytics in healthcare, clinical research, life science or other related organizations

+ Experience with Hemophilia, Duchenne's Muscular Dystrophy, growth hormone deficiency, rare cardiac conditions, or other Rare Disease priority areas highly desired

+ Two or more years of experience in two or more of the following:

+ Experience in clinical registry, patient generated health data, unstructured clinical data and other health data sources

+ Understanding global regulatory guidance for appropriate use and submission of RWE

+ Artificial Intelligence (AI) / Machine Learning (ML): ability and experience in creating advanced models to generate real world insights

+ Data Visualization: passion for and experience in generating easy-to-use, interactive data visualization capabilities (e.g., Tableau, PowerBI, Qlik, Spotfire, Looker)

+ Knowledge of efficient programming practices and the software development life cycle

+ Clinicogenomics: understand the clinical application of genomic, transcriptomic and other biomarker tests and result reports as they pertain to clinical care or research

+ Experience integrating real world evidence in early clinical development.

**Other Job Details:**

Last Date to Apply for Job: May 12th, 2021

Additional Location Information: New York, NY; Collegeville, PA; US - Remote


**Sunshine Act**

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

**EEO & Employment Eligibility**

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer.

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