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Medium — niche clinical-systems engineering requirement and seniority reduce density despite known CRO brand.
High — clinical trials and regulatory systems expertise is industry-specific and less transferable across sectors.
High — requires senior clinical-trials domain expertise, regulatory knowledge, and mandatory technical development skills.
Lead the design, development, and implementation of clinical systems ensuring compliance with functional and regulatory requirements.
Coordinate with cross-functional teams to define system needs and deliver solutions enhancing clinical trial management and data analysis.
Manage vendor and stakeholder relationships to deliver system updates and support while providing strategic system guidance and troubleshooting.
Degree in computer science, software engineering, or related field.
Extensive experience leading development and implementation of clinical systems with deep understanding of clinical trial processes and regulatory requirements.
Strong leadership skills with the ability to manage cross-functional teams and projects.
Willingness to travel approximately 15%.
Experienced in scientific operations and capable of managing competing priorities alongside team development.
Proficient in programming languages, system integration, and data management relevant to clinical systems.
Able to collaborate effectively with diverse teams and external partners to align technology with clinical research objectives.