Associate Project Manager - Advisory at Signant Health

As part of our team, your primary responsibilities will be: 

• Manage all phases of projects, including planning and client deliverables.
• Handle multiple projects, maintaining schedules and quality in a dynamic environment.
• Coordinate with Global Project Management and Technical Delivery teams.
• Oversee the development and approval of study materials, ensuring compliance with Quality Management governance.
• Facilitate Change Orders and maintain strong client relationships through consistent communication.

Key Accountabilities:

• As a staff member, the employee is expected to embrace and contribute to our culture of process improvement, focusing on streamlining our processes, adding value to our business, and meeting client needs.
• Responsible for compliance with Company Procedures in support of client deliverables
• Recognize, exemplify, and adhere to the company values, which center around our commitment to People, Clients, and performance

Decision-Making and Influence:

• Demonstrated ability to lead projects through influence.
• Capable of risks and making decisions that align with Signant values and strategy.
• Facilitate customer escalations effectively, with follow-up and closure.

You’ll need to bring: 

• Three to five years of professional experience.
• Skills in project management, including budgeting, resource allocation, and deliverable management.
• A degree or equivalent experience.
• Analytical, organizational, and problem-solving skills.
• Strong client and vendor relationship management.
• Proficiency in Microsoft Office and fluency in English.
• Willingness to travel for business.

We’d be thrilled to hear that you also have:

• One to two years of project management experience
• Background in Pharmaceutical, Medical Education, and CRO
• Experience in clinical trials/pharmaceutical industry/life sciences
• Ability to travel for business trips (overnight business trips could be expected quarterly)
• Experience/understanding of the clinical research environment and GCP principles is preferred.