Hybrid CTL Manager-Site & Enrollment Lead

Recordati; Bridgewater Township (NJ); Vor Ort; USD 110.000 - 165.000; Vollzeit

Benefits dieser Stelle

401(k) plan with company match

Medical, dental, and vision insurance

Paid time off

Winter shutdown

Life and AD&D insurance

Zusammenfassung

Recordati Rare Diseases, North America is seeking a Clinical Trial Liaison Manager (CTLM) to oversee site trial delivery, recruitment, and data quality from our North American operations. The role is hybrid with regular travel, based in North America and reports to the Director, Clinical Operations NA.

The CTLM will lead site relationships, monitor adherence to GCP/SOPs, and provide project management support across the clinical organization while ensuring regulatory compliance and effective

Qualifikationen

• Bachelor's degree in life/physical sciences.
• Minimum five years of clinical development experience in oncology.
• Experience with audits, regulatory inspections, and CAPAs.
• Experience with Phase 1-4 clinical development studies.
• Strong knowledge of GCP, CFR, and ICH guidelines.

Aufgaben

• Manage site/investigator relationships and sponsor-oversight activities.
• Oversee patient recruitment and enrollment efforts.
• Ensure data quality and regulatory compliance across trials (remote/on-site).
• Collaborate with CRAs, vendors, and local sites to share best practices.

Kenntnisse

English communication

Conflict resolution

Relationship management

Negotiation

Project management

Ausbildung

Bachelor's degree (life/physical sciences)

Tools

Microsoft Office

Clinical trial management systems

Jobbeschreibung

Recordati Rare Diseases, North America is seeking a Clinical Trial Liaison Manager (CTLM) to oversee site trial delivery, recruitment, and data quality from our North American operations. The role is hybrid with regular travel, based in North America and reports to the Director, Clinical Operations NA.

The CTLM will lead site relationships, monitor adherence to GCP/SOPs, and provide project management support across the clinical organization while ensuring regulatory compliance and effective