EHR Analyst – Real-World Evidence (RWE)



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EHR Analyst – Real-World Evidence (RWE)


Long term contract


We are seeking a highly skilled EHR Analyst to join our team in advancing our Real-World Evidence (RWE) capabilities within the pharmaceutical industry. This role will be instrumental in leveraging electronic health records (EHRs) and clinical data to drive insights that inform decision-making across various stages of drug development and commercialization.

Key Responsibilities:

  1. System Optimization: Collaborate with cross-functional teams to optimize EHR systems to efficiently capture, standardize, and integrate clinical data for RWE generation.
  2. Data Management: Design and implement data management strategies to ensure the quality, integrity, and security of clinical data collected from healthcare providers and clinics.
  3. RWE Analytics: Utilize advanced analytical techniques to analyze large-scale clinical data sets and derive meaningful insights that contribute to evidence generation for regulatory submissions, market access, and post-market surveillance.
  4. Protocol Development: Assist in the development of study protocols and analytical plans for RWE studies, ensuring alignment with regulatory requirements and industry best practices.
  5. Collaboration: Foster strong partnerships with healthcare providers, clinics, and research organizations to facilitate data sharing agreements and streamline data acquisition processes.
  6. Regulatory Compliance: Stay abreast of evolving regulatory guidance and industry standards related to RWE generation, ensuring compliance with relevant regulations such as GDPR, HIPAA, and 21 CFR Part 11.
  7. Cross-Functional Support: Provide technical expertise and support to cross-functional teams, including Medical Affairs, Market Access, Clinical Development, and Commercial teams, to incorporate RWE insights into strategic decision-making.


  • Bachelor's degree in Computer Science, Information Systems, Life Sciences, or related field; advanced degree (MS, PhD) preferred.
  • Proven experience (3+ years) working with NextGen, e-Clinical Works, or similar electronic health record (EHR) systems in a pharmaceutical or healthcare setting.
  • Strong proficiency in data manipulation, analysis, and visualization using tools such as SQL, Python, R, or SAS.
  • Familiarity with RWE methodologies, including retrospective cohort studies, observational research, and comparative effectiveness analyses.
  • Excellent communication and interpersonal skills, with the ability to effectively collaborate with diverse stakeholders and translate technical concepts to non-technical audiences.
  • Experience with regulatory submissions and compliance in a pharmaceutical or healthcare environment is desirable.
  • Demonstrated ability to thrive in a fast-paced, dynamic environment and manage multiple priorities effectively.

Medasource provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, national origin, age, sex, citizenship, disability, genetic information, gender, sexual orientation, gender identity, marital status, amnesty or status as a covered veteran in accordance with applicable federal, state, and local laws.


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