Remote Clinical Trial Master Scheduler (PMI-SP Certified)

Pharmica Consulting - Tarrytown, NY

We are looking for an individual to work closely with multiple stakeholder groups to plan, develop, update, and control schedules for clinical studies using Microsoft Project in a MS-Project Server environment.

On a typical day you might:

• Obtain activity status from stakeholders to update and maintain an accurate schedule.

• Develop new schedules using a template to identify what is to be done, when will it occur, and plan the sequence of work to be performed for a clinical study.

• Create a schedule baseline.

• Analyze variance between planned and actual performance. Propose options to take corrective actions to avoid delays and optimize the schedule.

• Communicate issues that could impact adherence to the baselines, to elevate awareness to relevant stakeholders.

• Perform “what-if” analysis to optimize a schedule.

• Improve and evolve the scheduling templates.

• Develop new templates and implement logic from those templates into schedules.

• Apply scheduling standards.

To be considered for this opportunity you must meet the three requirements identified below:

1. Bachelor’s degree. Master’s preferred.

2. Minimum of 5 years’ experience developing, updating, monitoring, and controlling schedules using MS-Project and MS-Project Server in a drug development or clinical development environment for 40+ clinical studies.

3. Project Management Institute (PMI) Scheduling Professional (PMI-SP) certification is required. PMI Project Management Professional (PMP) is optional.

Posted On: Friday, October 2, 2020

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