System Design Analyst II, Clinical Systems (Medidata RAVE)

BioSpace; North Chicago (IL); On-site; USD 120,000 - 180,000; Full time

Job summary

AbbVie Data Science is seeking a senior data systems specialist to drive design and delivery of clinical data systems. You will establish standards, ensure compliance with GCP/ICH, and align study design with protocol requirements.

Join a team that collaborates across functions to optimize data flow, integrate systems (EDC/IRT/ePRO), mentor colleagues, and push innovation while maintaining regulatory vigilance.

Qualifications

• 5+ years hands-on technical study build in EDC required.
• Experience with Medidata RAVE is required; Veeva EDC experience a plus.
• Strong knowledge of CDASH; SDTM knowledge required.
• Proven ability to influence others and coach in a matrixed environment.
• Effective written and verbal communication and strong analytical skills.

Responsibilities

• Develop common data standards and ensure designs comply with standards and protocol.
• Design and benchmark clinical trial systems to optimize functionality and data flow.
• Ensure TA- and program-level consistency in design work.
• Deliver new clinical systems on time and manage inter-system integrations.
• Collaborate with CDO and cross-functional teams to align objectives.
• Adhere to GCP, ICH, SOPs and local regulations; mentor team members.
• Lead cross-functional innovation and process improvements.

Skills

EDC study build

Medidata RAVE

Veeva EDC

CDASH

SDTM

Influence others

Communication skills

Analytical skills

Education

Bachelor's degree in business, MIS, CS, life sciences or equivalent

Masters preferred

Tools

Medidata RAVE

Veeva EDC

Job description

AbbVie Data Science is seeking a senior data systems specialist to drive design and delivery of clinical data systems. You will establish standards, ensure compliance with GCP/ICH, and align study design with protocol requirements.

Join a team that collaborates across functions to optimize data flow, integrate systems (EDC/IRT/ePRO), mentor colleagues, and push innovation while maintaining regulatory vigilance.