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Job Description:
Planning/Controlling (Scheduling and Resource Management) • Responsible for coordinating, monitoring and reporting project schedule and resource management information to enable alignment of PRD and partner line schedules and FTE/dollar resources. These schedules include: • Clinical study plans (Protocol Development to Final Clinical Study Report) and Clinical Operation Submission activities to support Module 1 and 5 of the submission plan. • Identifies and raises schedule conflicts, risks, and resource peaks/troughs appropriately for resolution. • Directly participates in and contributes to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates. • Monitors progress of project activities towards next project milestone, anticipates and highlights potential variances, supports line/team in critical path analyses and understanding the impact. • Performs scenario planning of project timelines within and across protocols and across disease area/portfolio to enable optimum use of local, general, and outsourced resources to ensure efficient delivery of project milestones. • Project Execution and Delivery • Partners with key team members (e.g., PM, Medicinal Sciences, CS&O;, DSRD, Commercial) to manage the project and achieve key milestones according to the endorsed timeline, cost, and quality parameters. • Contributes to risk management through the identification of operational and project/program risks for discussion with appropriate team leadership.



Participates in team discussions to de-risk projects and develop new options to resolve moderately complex issues. • Provides the Portfolio Management group with project schedule information to enable effective portfolio management activities. Analysis and Reporting • Produces what-if scenario analyses (base, optimistic and pessimistic development) based on context obtained from project team members (e.g. PM, Medicinal Sciences, CS&O;, DSRD, Commercial). Decisions taken by the team based on these analyses may impact project delivery, costs, and resource requirements. • Reviews own work regarding quality of schedule and resource metadata through utilization of quality reports and monitoring/management of such data with the team/line members. • Provides timely reporting to the PM, Portfolio Management, and project teams, alerting them to the possibility of endangered/missed or conflicting milestones and critical path activities. • Ensures regular information updates and analysis and interpretation of planning and forecasting data to project teams, Portfolio Management, platform lines, and management teams. • Utilizes available reporting and visualization tools to support governance and team reporting needs (e.g. OnePager, Business Objects, Spotfire).



• Provides context to local customers of reports generated globally and consolidates customer feedback to enable improvement of existing reports and generation of new reports. Process • Partners with project team members (e.g. PM, Medicinal Sciences, CS&O;, DSRD, Commercial) to identify opportunities and potential solutions to realize efficiency in the development process. • Contributes to continuous improvement of project plans, plan generation, plan utilization, and/or report creation/development processes. Qualification: Education • Bachelors level degree. • B.S. with 2+ years' experience or M.S. with 1-2 years' experience. Experience • At least 1 year experience in project planning and project management. • At least 2 years’ experience in pharmaceutical industry or related/similar industry. • Beneficial Relevant Capabilities • Project Management Professional (PMP) certification preferred but not required. • Experienced in end-game/regulatory submission planning and/or product launch planning. • Experienced with planning and resource forecasting tools (e.g., MS Project, Planisware, OnePager). • Experienced user of reporting and office software (e.g., MS Office, Business Objects, Spotfire). • Trained/experienced in negotiation, facilitation and managing cross-functional team dynamics. Key Skills: Portfolio Management; Pharma R&D; Drug Development; Project Management Professional (PMP) ; ‌PCC(Preclinical Candidate Compound); ‌IND (Investigational New Drug) ;‌NDA‌(New Drug Application)

📌 Insourced Project Planner (Perú)
🏢 Caidya
📍 Perú