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Job Description
Structured overview of role & requirementsAbout This Role
Lead technical development and study setup for Electronic Data Capture (eDC) solutions across multiple clinical studies, ensuring quality and timely delivery.
Oversee vendor and data acquisition activities, provide input on study design and planning, and manage risk and quality control for study-related deliverables.
Drive process improvements, training, and quality assessments in Data Acquisition; perform after-action reviews to share learnings and propose enhancements.
Minimum Requirements
Minimum 5+ years of experience in data acquisition or related roles in Clinical Research, Information Systems, or relevant scientific fields.
Proficient with eDC solutions such as Inform, Rave, Veeva CDMS Vault and ePro solutions.
Knowledge of multiple programming languages including PL/SQL, SAS, Python, C#.
Extensive working knowledge of GxP, ICH guidelines, and regulatory requirements governing drug development.
Ideal Candidate Profile
Experienced in managing complex clinical study data acquisition with measurable impact on study delivery and quality.
Technical proficiency in developing eDC applications and coordinating vendor deliverables within regulated clinical research environments.
Able to translate regulatory and operational requirements into effective data management solutions and process improvements.