Clinical Research Project Manager (Hybrid Work)

Utah; Salt Lake City (UT); Hybride; USD 47 000 - 77 000; Plein temps

Avantages offerts par ce poste

Healthcare coverage

14.2% retirement contributions

Paid leave time

11 paid holidays

Tuition reduction for employees

Flex spending accounts

Life insurance

Transit benefits

Professional development

Résumé du poste

University of Utah in Salt Lake City seeks a Clinical Research Project Manager to organize and oversee division clinical research activities, supporting both technical and administrative needs under the PEM division. You will assist the PI, develop study documents, and ensure compliance with university and regulatory requirements.

The role involves coordinating multi-site activities, maintaining IRB/FDA compliance, and communicating with sponsors and investigators.

Qualifications

• Requires strong project management skills and ability to coordinate clinical studies from initiation through delivery.
• Knowledge of regulatory requirements (FDA/HIPAA/IRB) and good clinical practices.
• Experience collaborating with sponsors, PIs, and research staff to meet study objectives.

Responsabilités

• Coordinate all aspects of clinical studies from initiation through delivery.
• Maintain records, ensure compliance with protocols and regulations.
• Manage budgets, timelines, and study milestones with cross-functional teams.
• Prepare regulatory submissions and track adverse events and study deviations.

Connaissances

Project management

Regulatory knowledge

IRB familiarity

Clinical research coordination

Formation

Bachelor's degree in related field

Outils

IRB systems

EDC databases

Description du poste

University of Utah in Salt Lake City seeks a Clinical Research Project Manager to organize and oversee division clinical research activities, supporting both technical and administrative needs under the PEM division. You will assist the PI, develop study documents, and ensure compliance with university and regulatory requirements.

The role involves coordinating multi-site activities, maintaining IRB/FDA compliance, and communicating with sponsors and investigators.