Onsite Clinical Data Associate — DM & UAT Specialist

Smart IMS Inc; Bridgewater Township (NJ); On-site; USD 48,000 - 76,000; Full time

Job summary

Smart IMS Inc is seeking a Clinical Data Associate in Bridgewater, NJ (onsite) for a 12-month contract. You will support DM study leads, edit DM documents, and perform data reviews and reconciliation in a compliant, timely manner.

Responsibilities include updating DM plans, performing UAT, and ensuring high-quality data management through cross-functional collaboration. A2+ years in CDM and Medidata Rave experience are desired.

Qualifications

• Minimally 2 years of clinical data management experience in biotech, pharma, or CRO environments.
• Hands-on experience with EDC systems, Medidata Rave preferred.
• Excellent written and verbal communication skills.
• Experience working in cross-functional teams.
• Strong organizational skills and attention to detail.

Responsibilities

• Edit and update DM documents and study plans under DM lead guidance.
• Conduct UAT testing, data review, and discrepancy management.
• Reconcile external data to the clinical study database and perform SAE reconciliation.
• Track issues, generate data listings, and file DM documents in trial master files.
• Ensure DM procedures are followed consistently and provide high-quality services.

Skills

Clinical data management

Excellent communication

Cross-functional teamwork

Organizational skills

EDC experience

Education

Associate's degree or higher

Tools

Medidata Rave

Job description

Smart IMS Inc is seeking a Clinical Data Associate in Bridgewater, NJ (onsite) for a 12-month contract. You will support DM study leads, edit DM documents, and perform data reviews and reconciliation in a compliant, timely manner.

Responsibilities include updating DM plans, performing UAT, and ensuring high-quality data management through cross-functional collaboration. A2+ years in CDM and Medidata Rave experience are desired.