Clinical Lead: Site Activation & Delivery

Premier Research Group; États-Unis; Sur place; USD 104 000 - 128 000; Plein temps

Avantages offerts par ce poste

Health insurance

Retirement plans

Paid time off

Résumé du poste

Premier Research seeks a Clinical Lead - Senior Site Activation Lead to join our Clinical Management team in the United States. The role focuses on delivering timely site activations for biotech, medtech, and specialty pharma programs while upholding ICH/GCP standards.

You will collaborate with functional leads to drive quality, manage budgets, and lead kickoff meetings to align objectives, timelines, and study start-up strategies.

Qualifications

• Undergraduate degree in clinical, science, or health-related field
• 5 years professional experience in CL, RSM, PM, or SSUA or equivalent
• Demonstrated leadership of a team across study start-up and other functions
• Understanding of project budgets and timelines
• Excellent interpersonal and communication skills
• Strong knowledge of ICH/GCP regulations

Responsabilités

• Coordinate with functional leads to deliver site activation and ensure quality delivery per contract
• Lead Site ID Kick Off Meetings and align objectives, timelines and strategy
• Oversee SSU and clinical activation deliveries in line with project timeline and update projections
• Collaborate with cross-functional teams to finalize country mix and site selection
• Escalate risks to PM and Sponsor and propose mitigation strategies
• Oversee CTMS data entry through activation and justify delays with contingency plans
• Monitor activation status and provide updates to team and client weekly

Connaissances

Leadership

Team leadership

Project management

Budget awareness

Stakeholder management

Communication

Formation

Bachelor's degree in clinical/science/health

Outils

CTMS

Description du poste

Premier Research seeks a Clinical Lead - Senior Site Activation Lead to join our Clinical Management team in the United States. The role focuses on delivering timely site activations for biotech, medtech, and specialty pharma programs while upholding ICH/GCP standards.

You will collaborate with functional leads to drive quality, manage budgets, and lead kickoff meetings to align objectives, timelines, and study start-up strategies.