What are the responsibilities and job description for the Specialist 3 - Resource Planning position at jnj?
Johnson & Johnson Family of Companies
Title: Resource Planning Specialist
Location: Titusville, NJ
Duration: 1 year
Pay Rate: $ 74.73
Benefits on offer for this contract position: Health Insurance, Life insurance, 401K and Voluntary Benefits
Please note that this is a contract role providing services to the Johnson & Johnson Family of Companies through external staffing partners of Kelly OCG. If you are selected for this role, you will be employed by a contract staffing supplier and will not be a member of the Johnson & Johnson Family of Companies.
Summary:
Develops and implements integrated preclinical programs and activities to support clinical plans from early development through product registration.
Responsibilities:
- Performs integrated preclinical programs and activities to support clinical plans from early development through registration.
- Serves as a function planner to support/track preclinical planning process. Identifies appropriate suppliers, coordinating system utilization, contract development, negotiation, and project and relationship management.
- Plans scheduling information for update of project/study plans.
- Provides management, finance and relevant groups with resource and capacity estimation of programs.
- Supports study tracking and planning procedures for preclinical by reviewing and updating study specific information in collaboration with project leaders, management and other planning team associates.
- Ensures standard processes are utilized in procedures.
- Supports business planning scenarios and provides information to leadership on metrics assessment.
- Provides metrics and analysis in support of best-in-class practice.
- Represents preclinical at compound team meetings and various committee meetings.
- Coordinates the allocation of resources and schedule with the preclinical group.
- Develops reports and data analysis to plan the workflow through clinical research.
- Assists in regulatory submissions and participation in clinical safety reviews.
- Assists in training new planners and key study and management personnel.
Qualifications:
- Develops and implements integrated preclinical programs and activities to support clinical plans from early development through product registration.
- Requires 4-6 Years Work Experience Education Required: University/Bachelor's Degree or Equivalent
- Must have experience with Planisware, MS Office, Tableau.
Salary : $75
