Lenox Executive Search is seeking to fill a contractual role with one of our global pharmaceutical clients for a Senior Manager, Regulatory Affairs Global SubmissionManagement. This is a one year contract with possible extension.

The Senior Manager, Regulatory Affairs Global Submission Management is responsible for the planning, managing and tracking of the regulatory portfolio of submissions for an assigned program. This role will be responsible for developing comprehensive plans and reports that would include all major milestones and other key dates related to the filings. The plans would beused within regulatory to plan submission activities and resources. In addition, the plans will need to be integrated cross-functionally to ensure project team alignment on major milestones. This role will be responsible for identifying timeline risk mitigation and contingency planning within plan. This role will collaborate with key functions to collect the latest dates, understand the change drivers, update the plan and run and distribute reports to the various stakeholders.

Key Duties and Responsibilities Senior Manager, Regulatory Affairs Global Submission Management:

• Leads complex project plans from project initiation to closeout.

• Facilitates the definition of the project milestones, tasks, deliverables,key dependencies and resource requirements.

• Develops complex project plans, status reports, issue logs, andother project-related artifacts.

• Identifies facilitating strategies for risk mitigation and contingency planningwithin plan.

• Identifies and resolves complex project plan issues and takes a newperspective on existing solutions.

• Communicates project status, difficult or sensitive issues, scheduleand accomplishments to various management and stakeholder groups, as needed, and works to build alignment

• Prepares necessary reports to drive data-driven resource, budget andtrade-off discussions across GRA function

Knowledge and Skills Senior Manager, Regulatory Affairs Global Submission Management:

• Experience in regulatory filing project management

• Expertise in project management tools

• In-depth conceptual knowledge of types of Global HA submissionsand requirements and guidelines

• Ability to work with firm deadlines and adapt quickly to changing requirementsand priorities

• Excellent organization, written/verbal communication, andattention to detail to explain difficult information and works to build alignment

• Stakeholder management skills

• Ability to balance multiple tasks to meet priorities and timelines

Education and Experience Senior Manager, Regulatory Affairs Global Submission Management:

• Bachelor’s degree in life sciences or technology area

• Typically requires 6 years of project management experience inregulatory/clinical project management or project management experience in a life sciences company, or the equivalent combination of education and experience

Job Type: Contract

Pay: $60.00 - $70.00 per hour

Schedule:

• Monday to Friday

Education:

• Bachelor's (Required)

Experience:

• Clinical/ Regulatory Project management: 6 years (Preferred)
• global HA submissions: 6 years (Preferred)

Work Location: One location

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