Application Implementation Specialist

🕒 July 7

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Advarra

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 1983

☁️ SaaS

💊 Pharmaceuticals

SaaS • Pharmaceuticals

Advarra is a provider of integrated regulatory oversight and clinical trial technology, combining independent IRB review and compliance services with enterprise SaaS platforms (including Braid, OnCore, Clinical Conductor, eReg, and eSource). The company delivers operational intelligence, AI-powered protocol design and automation, site collaboration, study startup and enrollment tools, and strategic enablement services to sponsors, CROs, research sites, and institutions to improve efficiency, compliance, and patient safety across the clinical trial lifecycle.

📋 Description

• Master complex software applications, integrations and reports • Work with new customers to fully understand their current business processes and workflows • Map current state workflows into new, future state application workflows using process flow charting • Develop and utilize use cases to analyze, define and document business requirements and application scenarios • Provide guidance to internal stakeholders on customer enhancement requests • Coordinate with other internal teams to develop Statements of Work (SOWs) • Assist in the completion of technical RFP questions for prospective customers • Build a strong relationship with the customer project team • Provide guidance to customers on best practices for integrating Advarra technology solutions into their research operations environment • Work closely with the implementation project manager to ensure on-time delivery of all milestones • Perform other job-related duties as assigned.

🎯 Requirements

• Bachelor’s Degree or relevant experience • 5-8 years’ experience in healthcare technology (clinical research experience preferred) • Strong analytical thinking skills • Strong client communication skills • Strong oral presentation skills • Familiarity with EDC, EMR/EHR and other clinical trial information systems • Deep familiarity with Clinical Trial Management Systems (CTMSs) • Subject Matter Expert in eClinical solutions such as eRegulatory, eSource and eConsent preferred • Understanding and experience with integrating a CTMS to other common systems (e.g. EMR, EDC, EMPI) • Understanding and experience with operational and regulatory reporting that services clinical research • Understanding of clinical research finances

🏖️ Benefits

• health coverage • paid holidays • variable bonus