• Location: Lawrenceville, NJ (hybrid - will be on-site weekly in Lawrenceville, NJ)
• Duration: 6 months with potential to extend/convert
• Benefits : Medical, dental, vision insurance, 401K match, etc
• Pay Rate: $68.50 to $88.50 / hour based on experience

The candidate must be able to work 50% onsite at Lawrenceville, NJ so local candidates only please.

Must Haves:

• Experience working with operational clinical trial data / clinical trial performance metrics
• Ability to summarize complex data
• Ability to identify trends, risk and issues in data
• Highly effective written and verbal communication and interpersonal skills
• Ability to effectively communicate with functional Sr. Leadership
• Strong presentation and facilitation skills

Position Summary :

Position is accountable for supporting with the Executive Director, Global Development Operations (GDO) and team to support management of operations portfolio governance and other business operations related directives and tasks.

Position Responsibilities:

The position may include, but not be limited to the following activities:

• Collaborate across Global Development Operations functional leadership to prepare and facilitate Portfolio Review Meetings and Operational Deep Dive Sessions
• Ensure proactive identification and triage of risk and issues to enable the delivery of the operational portfolio.
• Assess trends to develop recommendations for improvement of future clinical trial delivery.
• Liaison with R&D enterprise governance teams
• Lead or support Global Development Operations Book of Work maintenance
• Lead or support standard and ad hoc Global Development Operations strategic reporting requests
• Partner with R&D BIA team on evolution of Global Development Operations analytical needs
• Assist Executive Director, Sr. Director or Director Business Operations team members to drive successful delivery of key initiatives.
• Support other key business operations tasks, analyses and deliverables as required.

Degree Requirements: Bachelor’s Degree

Experience Requirements : 5 years

Key Competency Requirements :

• Experience working with operational clinical trial data.
• Robust understanding of biopharmaceutical industry, clinical trial conduct, regulatory and safety processes, and the external and internal Business Environment
• Knowledge of GCP/ICH guidelines and regulations
• Ability to work both independently and collaboratively within a matrixed environment.
• Highly effective written and verbal communication and interpersonal skills
• Strong presentation and facilitation skills
• Strong business acumen
• Capable of innovative thinking and bringing new ideas to improve current state.