Oncology Clinical Project Leader – Global Trials

Precision Medicine Group; United States; Remoto; USD 110.000 - 165.000; Tempo pieno

Descrizione del lavoro

Precision for Medicine seeks a Clinical Project Manager / Senior Clinical Project Manager with oncology expertise to oversee full‑service global and regional Ph I–IV trials in a CRO setting. You will manage delivery, timelines, budgets, and cross‑functional teams across regions, ensuring quality and strategic trial execution.

You will lead studies from proposal through delivery, liaise with sponsors and senior management, ensure GCP/ICH compliance, and travel domestically and internationally as

Competenze

• Degree or related life science qualification and experience.
• Previous full-service/global PM role in CRO essential.
• Experience managing oncology studies and overseeing CRO trial delivery.
• Familiar with GCP/ICH guidelines and clinical development processes.

Mansioni

• Lead clinical projects within budget and scope; may run international trials.
• Serve as primary client liaison; participate in proposals and presentations.
• Coordinate with sponsor and Precision teams, including senior management.
• Manage all aspects of a clinical trial; include data, safety, and statistics.
• Prepare status updates and define deliverables and success metrics.
• Act as a core Project Team member to ensure efficient execution.
• Prepare and review protocols, project plans, consents, site contracts, and budgets.

Conoscenze

Oncology clinical trials

CRO project management

English proficiency

Travel willingness

Stakeholder management

Cross-functional collaboration

Formazione

Degree in life sciences

Strumenti

MS Office

MS Project

PowerPoint

CTMS

eTMF

EDC

IXRS

Descrizione del lavoro

Precision for Medicine seeks a Clinical Project Manager / Senior Clinical Project Manager with oncology expertise to oversee full‑service global and regional Ph I–IV trials in a CRO setting. You will manage delivery, timelines, budgets, and cross‑functional teams across regions, ensuring quality and strategic trial execution.

You will lead studies from proposal through delivery, liaise with sponsors and senior management, ensure GCP/ICH compliance, and travel domestically and internationally as