Senior Clinical Program Manager - Trials & Strategy

Planet Pharma; Redwood City (CA); On-site; USD 130,000 - 170,000; Full time

Job summary

Planet Pharma is seeking a Clinical Program Manager (CPM) in Redwood City, CA to drive operational strategy across clinical programs and trials. You will govern timelines, budgets, and cross-functional decision-making while mentoring CTMs and coordinating with CROs and vendors.

The role requires 8+ years in pharma/biotech clinical operations or research, strong FDA/EMA knowledge, and the ability to manage multiple trials and budgets with a strategic, data-driven approach.

Qualifications

• BS, BA, or RN in a relevant scientific discipline.
• 8+ years of relevant experience in pharma/biotech,Clinical Ops or Clinical Research.
• Expert knowledge of FDA/EMA Regulations, ICH Guidelines, GCP.
• High-level cross-functional collaboration and program-level planning.
• Ability to analyze operational data and drive decisions.
• Travel up to ~25%.

Responsibilities

• Provide expert leadership on complex assignments and drive trial execution strategy across programs.
• Lead the Clinical Study Execution Team (CSET) meetings to ensure timelines are met.
• Develop trial execution strategies and timelines across studies.
• Oversee CROs/vendors to ensure study delivery and budget considerations.
• Mentor CTMs, CTMAs, and CTAs in clinical operations.
• Maintain audit/inspection readiness and TMF compliance.
• Collaborate on protocol and study document drafting with cross-functional partners.
• Participate in CRO/vendor RFP development and selection.

Skills

Cross-functional collaboration

Strategic planning

Risk management

FDA/EMA knowledge

Study budgeting

Vendor management

Leadership

Travel readiness

Education

BS/BA or RN in relevant discipline

Job description

Planet Pharma is seeking a Clinical Program Manager (CPM) in Redwood City, CA to drive operational strategy across clinical programs and trials. You will govern timelines, budgets, and cross-functional decision-making while mentoring CTMs and coordinating with CROs and vendors.

The role requires 8+ years in pharma/biotech clinical operations or research, strong FDA/EMA knowledge, and the ability to manage multiple trials and budgets with a strategic, data-driven approach.