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Mar 31, 2026

Subject Matter Expert - Essex Management

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Overview: Subject Matter Expert - Essex Management    This is a Part-Time role.   US Remote   This position supports "Essex, an Emmes Company". Essex is a biomedical informatics and health information technology-focused consultancy founded in 2009 and headquartered in Rockville, MD. The Essex team comprises experts with extensive experience in strategically developing and managing complex health and biomedical information programs for clients in the Federal Government, research academia, and private sectors.    Emmes Group: Building a better future for us all.   Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.   We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!   Primary Purpose   The Subject Matter Expert (SME) demonstrates advanced knowledge and technical capabilities in the design and implementation of Health Information Technology (HIT) systems, clinical database architectures, semantic infrastructures, and/or data standards associated with healthcare or clinical data.  Responsibilities: - Advising project teams on adoption of architectures or data standards  - Assess customer needs and advise on solutions based on requirements  - Provide services to develop scalable and regulatory compliant data architectures and systems  - Lead tasks as required in order to fulfill project objectives  Qualifications: - Bachelor’s Degree in relevant field and 20+ years of experience required; or master’s degree and 10+ years of experience required; or Ph.D. / MD (preferred) - Certifications in relevant technical disciplines highly preferred - Deep knowledge of clinical and health information technology standards relevant to client project – such as HL7, CDISC, DICOM, RM-ODP, 21 CFR Part 11, etc.  - Deep knowledge of relational databases pertinent to the delivery of regulatory compliant technology solutions  - Leadership role in professional organizations and/or standards bodies highly preferred   CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes   The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.   #LI-Remote