The Project Coordinator within FSP Solutions will be responsible for providing operational support to Project Managers and scientific program leaders from the cross-functional translational research and OTR teams for one of our sponsors.
This is a hybrid role requiring a minimum of 3 days onsite in Spring House, PA or in Titusville, NJ, as well as 1-2 days per month travel between sites.
Essential Duties and Responsibilities
- Support the operational management of multiple teams/stakeholders in a fast-paced, cross functional environment for low complexity projects
- Coordinate agenda, track key actions/decisions, support stakeholders in task completion, collaboration and communication within translational research (TR) teams
- Support cross-functional planning, budgeting, and resourcing activities while managing Key event maps (KEM) - timeline of costs and events
- Provides support for strategic biomarker plans for trials (ensure creation and regular updates)
- Assist with identifying and developing process improvement initiatives
- Supports the delivery of TR status updates
- Escalation of risks and proactive risk management
- Align timelines across drug development path for a project
- Understand decisions' flow in TR
- Support TR teams and Project Managers during strategic budget review meetings where 'early budget read' is created
- Partner with Project Managers, Biomarker and Translational Leaders to oversee budgets, create budget line items and ensure accurate projection to alleviate risks and drive continuous improvement.
- Use technology solutions to support cross-functional translational research/OTR and Biomarker teams.
- MS Teams (ex. Planner, enable team calendar), PPT, One Note, SharePoint, MS Project
- Portfolio Dashboard (ex. Project view, team membership, milestones, trial timelines, upcoming project/work, budget, etc.)
- Building capabilities within Planisware, Tableau VizCafe
- Enable Key Performance Indicators (KPIs) and metrics (Tableau)
Education and Experience
- B.A./B.S. in Physical Sciences/Life Sciences or related scientific field required
- Entry level with some relevant industry experience (>2 years)
- Some experience managing projects, timelines, budgeting and forecasting preferred
- Understanding of drug development and clinical trial processes preferred
- Some sample management, analysis or sample tracking knowledge preferred
- Proficient with computer literacy; MS Office, MS Project, Smartsheet and SharePoint
- Demonstrated time management skills and organizational skills with the ability to plan, prioritize, and execute project tasks
- Excellent interpersonal skills
- Strong verbal and written communication skills
Supervisory Responsibilities
None
Physical Demands
- Prolonged periods of sitting at a desk and working on a computer.
- Prolonged use of computer and headphones for conference calls.
- Communicate effectively via phone, video, and email.
- Use hands and fingers to operate a computer and other office equipment.
Other Considerations
- Hybrid role, requiring up to 3 days per week on site in Spring House, PA or in Titusville, NJ. Other days are remote.
- Ability to work and/or be available for meetings during the East Coast core working hours of 9am-5pm, with flexibility to accommodate global time zones for meetings.