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Job #02673

About our client Our client is a human health care company seeking innovative solutions in disease prevention, cure and care for the health and well being of people worldwide. Position Location Associate Director/Project Manager (Oncology) New Jersey Salary Highly competitive package, commensurate with experience Responsibilities 1) Assist in the global development of oncology compounds 2) Interface with the Oncology TA, IPTLs and Global Team members in clinical operations, regulatory affairs, data management, statistics, finance and medical writing 3) Plan, direct and coordinate activities of designated oncology projects to ensure that the objectives of these projects are accomplished within the prescribed time frame and funding parameters 4) Ensure that all projects in assigned areas proceed in agreement with RDMC (timelines and priorities) 5) Monitor the progress of every project against defined milestones and timelines 6) Liaise with operating groups to inform the status 7) Help in advancing projects through the working knowledge of related disciplines 8) Facilitate resolution of project conflicts across therapeutic and operational areas by working with project teams 9) Develop innovative solutions resulting in timely execution of plans 10) Manage and develop a team of Direct Reports using appropriate formal and informal processes 11) Mentor individuals and ensure efficient allocation of resources within the team 12) Provide leadership both within and outside functional area, for global development initiatives such as taskforces and committees working to improve quality, efficiency and timeliness of work processes 13) Lead problem-solving with an enterprise-wide perspective 14) Facilitate identification of issues by teams and propose solutions for the timely and efficient execution of project plans 15) Work closely with the IPTLs to ensure that teams have the information required to achieve the business and project objectives 16) Guide and assist teams in preparing and reviewing documents, including IBs, contracts, development plans, protocols and study reports 17) Develop and implement procedures for monitoring projects 18) Oversee work outside area of direct accountability and across the company's geographic boundaries Requirements 1) Bachelor's degree in an associated functional discipline 2) 8+ years of experience of working in a project management capacity within the pharmaceutical industry 3) Experience in project management 4) Demonstrated experience in leading cross-functional and cross-national teams 5) Experience of working in complex team environments with numerous/diverse stakeholders 6) Superb understanding of the clinical development process 7) In-depth understanding of drug development plans, clinical development process, pre-clinical toxicology, CMC, statistics and regulatory requirements related to drug development 8) Ability to work independently with strong organizational, prioritization and analytical skills 9) Ability to manage multiple projects simultaneously 10) Excellent verbal, written and interpersonal skills