5+ years of experience in building RTSM and/or DHT clinical trial systems and developing user requirement with detailed understanding of requirements gathering, configuration, design, and user acceptance testing.
Excellent technical and data standard experience.
Proven awareness and experience in the use of data standards within a clinical trial environment; knowledge of industry standards such as CDISC SDTM is preferred.
Ability to create and explain business process and train others on that process.
Strong analytical and problem-solving skills.
Ability to resolve issues independently with good judgement to escalate appropriately.
Client focused and demonstrating an ability to create and maintain trust with the client.
Knowledgeable in ICH and GCP regulations in relevant geographies.
Personal leadership, prioritization and management of own workload.
Ability to conduct root cause analysis in business problem solving and process improvement development.
Excellent interpersonal, verbal, and written communication skills.
Knowledge in clinical research industry, including expert understanding of clinical technology, RTSM design, and system requirements.
eCOA, ePRO experience is a plus.
