[Hiring] Clinical Trial Planner @Syneos Health

Role Description

Clinical Trial Planner in Spain or Poland. FSP.

• Develop comprehensive Clinical Sub Team / study timelines from protocol concept through database lock and closeout, ensuring connectivity with the Asset Level Plan.
• Coordinate across a range of stakeholders inclusive of the Clinical Project Manager and the Asset Operations Lead / Asset Planner.
• Identify critical path activities and schedule dependencies.
• Build and maintain scenario-based plans.
• Forecast milestone delivery dates using data-driven assumptions.
• Assess impacts of changes and recommend mitigation strategies.
• Support IPSEN in building / refining templated Clinical Sub-Team Plans / Study Plans.
• Establish Clinical Sub Team planning governance and tracking mechanisms ensuring fit with overall Asset Level Planning processes.
• Support the CPM to manage risks, issues, assumptions, and dependencies.
• Monitor progress against baseline plans.
• Support resource and capacity planning activities.
• Work with the CPM to drive accountability for milestone achievement.
• Present schedules and forecasts in executive-friendly formats.
• Develop clear planning dashboards.
• Communicate risks and recovery plans effectively.
• Tailor messaging for operational and leadership audiences.
• Deep expertise in use of planning tools - OnePlan preferred but Plannisware or similar is acceptable.
• Good understanding of the overall Clinical Trial planning eco-system e.g. CTMS/OnePlan etc.
• Capture lessons learned.
• Standardize planning methodologies.
• Improve forecasting accuracy.
• Drive operational excellence initiatives.
• Champion best practices and innovation.
• Own study-plan quality and completeness (e.g., quality reviews).
• Prepare and conduct training to CDO colleagues to support adoption of study-level OnePlan standards and tools, as needed.
• Act as CDO SME on planning template and process.

Company Description

• Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
• No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.