job description - Associate Project Manager - Advisory
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.
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We are focused on leveraging software, deep therapeutic and scientific knowledge, and operational expertise to consistently capture, aggregate, and reveal quality evidence for clinical studies.