Senior Clinical Data Manager — Lead CDM & Data Quality (Hybrid)

Ctifacts; United States, Northern America, Americas; Hybrid; USD 85.000 - 115.000; Vollzeit

Benefits dieser Stelle

Health benefits

Hybrid work opportunities

Paid parental leave

Vacation package

Zusammenfassung

CTI Clinical Trial and Consulting Services is seeking a CDM lead to supervise and mentor a global CDM team, ensuring study deliverables meet quality standards and timelines. The role requires strong regulatory understanding and data integrity oversight across projects and sponsors.

Responsibilities include maintaining study documentation, budgets, and GSOP adherence, plus coordinating data from labs, ECGs and adverse events. Hybrid work options are available.

Qualifikationen

• Bachelor's degree in nursing or life science or equivalent
• Minimum 5 years of Clinical Data Manager experience in pharma/CRO
• 2 years of relational database experience
• Experience with Medidata Rave or OmniComm, TrialMaster

Aufgaben

• Direct activity of CDM team members to complete project deliverables on schedule
• Serve as CTI CDM representative on project teams
• Maintain CDM study files and budget
• Monitor data quality and GSOP compliance
• Provide project training and mentorship to CDM team
• Coordinate data receipt from external sources and reconciliation

Kenntnisse

Clinical Data Management

Regulatory knowledge

Communication skills

Process improvement

Ausbildung

Bachelor's degree in nursing or life science

Tools

Medidata Rave

OmniComm

TrialMaster

Jobbeschreibung

CTI Clinical Trial and Consulting Services is seeking a CDM lead to supervise and mentor a global CDM team, ensuring study deliverables meet quality standards and timelines. The role requires strong regulatory understanding and data integrity oversight across projects and sponsors.

Responsibilities include maintaining study documentation, budgets, and GSOP adherence, plus coordinating data from labs, ECGs and adverse events. Hybrid work options are available.