Clinical Solutions Analyst

Piper Companies is seeking a Clinical Solutions Analyst who understands software and computerized systems in the clinical trial process. The Clinical Solutions Analyst will be remote, supporting a Raleigh, NC headquarters.  

Requirements for the Clinical Solutions Analyst include:

-       Collaborate with relevant business users (clinical project managers, clinical research associates, data managers, etc) to understand solution requirements, develop and document business processes, and provide ongoing support for the solutions.

-       Work closely with IT counterparts who are primarily responsible for the technical aspects of the implemented clinical solutions.

-       Support and enhance best practices within the Clinical Solutions team to ensure the successful management of clinical trial technology solutions.

-       Engage with geographically diverse stakeholder groups.

Qualifications for the Clinical Solutions Analyst include:

-       7+ years of experience at a pharmaceutical/biotechnology company or CRO

-       5+ years of relevant experience

-       Must be Veeva certified

-       Understands solutions such as Electronic Data Capture (EDC) and Clinical Trial Management System (CTMS)

-       Experience with Metadata Repository (MDR), electronic Trial Master File (eTMF), and electronic Patient Reported Outcomes (ePRO)

-       Conducted GxP-aligned validation activities

-       Managed and supported various clinical trial technologies.

-       Proficient with BI reporting/dashboards

-       Bachelors degree in a related field

Compensation for the Clinical Solutions Analyst includes:

-       Hourly rate: $50-$65

-       Comprehensive benefit package: Medical, Dental, Vision, 401k match plus PTO, Sick leave as required by law, and Paid Holidays

Keywords: Clinical solutions analyst, solutions analyst, electronic trial master files, eTMF, clinical trial management system, CTMS, electronic data management, EDC, electronic patient report outcomes, ePRO, clinical trial operational reporting, reporting, data management, data, clinical trial managers, clinical research associate, CRA, information technology, IT, engagement plans, develop, performance qualification, PQ, validation documents, training, audits, audit, pharmaceutical, biotechnology, CRO, metadata repository, MDR, GxP aligned validation, Power Bi, SQL, drug development, dashboards, standard operating procedures, SOP, system development life cycle, SDLC, process data owner, PDO, clinical research organization

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This job opens for applications on 5/11/2025. Applications for this job will be accepted for at least 30 days from the posting date.