Program Manager / Prof

Program Manager / Prof
  • Competitive
  • Temporary
  • Woodcliff Lake NJ, US Woodcliff Lake Bergen County US 07677
Job Ref: JO000117244
Sector: Administrative / Clerical
Sub-sector: Professional Service
Date Added: 28 September 2021

    Director, Clinical Development Project Management

    At SRG, we create meaningful connections that empower individuals and businesses to shape tomorrow’s world.

    Working as part of the SRG team, you will work with our client which are Pharmaceutical or Bio-Pharmaceutical companies to ensure work quality and accuracy for our client in the Bio Pharmaceutical Industry. The Director, Clinical Development Project Management will oversee and manage clinical development programs from a Project Management perspective. Serves as a liaison between project management and planning, project team, and line management. Reviews status of projects and budgets, manages schedules, and prepares status reports. Assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction goals and objectives. Develops mechanisms for monitoring project progress and for intervention and problem solving with project managers, line managers, clients and other stakeholders.

    Summary of Key Responsibilities

    The qualified candidate will manage assigned project (s), including program’s strategic direction, integrated project plan, alliance management, cross-functional deliverables as required by the International Project Team. This role requires interaction with, and management of, internal cross-functional team members, business partners, and contractors.
    Essential Functions

    • Oversees the development of compounds from candidate selection to NDA/MAA filing for the assigned project (s) in the Neurology Business Group, in accordance with agreed to development plans and corporate objectives.
    • Advanced understanding of clinical research and the clinical drug development process
    • Advanced understanding of the Neurology therapeutic area
    • Advanced understanding of the drug development plans, preclinical toxicology, toxicology, CMC, regulatory and other development requirements as they relate to efficient execution of the development plans.
    • Advanced understanding of clinical trial management, including general understanding of all specialized support functions.
    • Budget management
    • Ability to effectively prioritize work and engage in creative problem solving to manage global projects.
    • Pro-actively identify, analyze and resolve project issues to ensure project milestones are met and projects are completed, with quality, on time and within budget.
    • Ability to work independently, with strong organizational, communication and interpersonal skills (works well with all levels of staff in a professional manner)History of working in complex team environments with numerous and diverse key stakeholders in multiple regions


    • Bachelor’s degree is required. An advanced degree is desirable (MS or PhD).
    • PMP is desirable.
    • Minimum of 12+ years’ experience in clinical project management; deploying project management methods; influencing work processes that span across departments and geographic boundaries.
    • Effective leadership and participation in global initiatives.

    SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

      30/10/2021 12:00:00
      USD 0.00 0.00 Hour
      Contact Consultant:
      Brian Houston

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