Associate Director, Project Management

Posted 5 days ago

This is a fully remote position, open to applicants in United States.

πŸ“‹ Description

β€’ Oversee one or more early-stage global Orexin development initiatives through project management.

β€’ Collaborate with the Global Team Leader to coordinate cross-functional matrix development teams and selected sub-teams.

β€’ Lead and continuously update comprehensive, cross-functionally integrated program Gantt charts, complete with dependencies and tailored summary views.

β€’ Identify and manage interdependencies, critical paths, and activities that may be at risk for effective scenario planning and risk management.

β€’ Create and maintain dashboards to communicate project status and monitor progress.

β€’ Facilitate cross-functional team meetings, including scheduling, agenda preparation, presentation materials, minutes, and follow-up on action items.

β€’ Develop and manage issue logs and risk registers to ensure timely resolution of issues and appropriate risk mitigation strategies.

β€’ Collaborate with cross-functional teams and Finance to create and update budgets while managing program expenditures within approved limits.

β€’ Oversee selected external vendors, managing timelines, budgets, MSA/SOW documents, and the integration of deliverables.

β€’ Assist in the preparation of Governance and Executive presentations.

β€’ Support the planning and creation of documents that meet quality standards for Regulatory/Health Authority submissions.

β€’ Contribute to the development and enhancement of best practices, processes, and procedures.


⛳️ Requirements

β€’ Bachelor's degree with 8+ years of experience in a pharmaceutical/biotech R&D setting, or a Master's/MBA with 6+ years in a similar environment, including 4+ years as a Project Manager or in a comparable role.

β€’ Experience in managing project teams through IND-enabling activities, pre-IND meetings, IND submissions, and Phase 1 development processes.

β€’ Demonstrated expertise in drug development and registration, encompassing early- and late-stage clinical, nonclinical, CMC development, as well as global regulatory interactions, submissions, and reviews.

β€’ Highly motivated, proactive, detail-oriented, and organized self-starter.

β€’ Strong communication, collaboration, interpersonal, and influencing abilities to achieve outcomes without formal authority and ensure optimal team performance.

β€’ Excellent analytical skills with experience in facilitating team decision-making.

β€’ Proficient in applying decision analysis methodologies and related tools.

β€’ In-depth knowledge of project management principles and practices.

β€’ Ability to excel in a fast-paced, dynamic environment.

β€’ PMP certification is highly preferred.

β€’ Advanced proficiency in project management software, such as Smartsheet.


🏝️ Benefits

β€’ Company bonus based partially on both company and individual performance.

β€’ Company-sponsored 401(k) plan.

β€’ Pension plan.

β€’ Vacation benefits.

β€’ Medical, dental, vision, and prescription drug coverage.

β€’ Flexible benefits, including healthcare and/or dependent daycare flexible spending accounts.

β€’ Life insurance and death benefits.

β€’ Time off and leave of absence benefits.

β€’ Well-being benefits, including an employee assistance program, fitness perks, and opportunities for employee clubs and activities.

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