Global Study Planning Manager
hace 4 semanas
ICON has an exciting new opportunity for a Global Project Manager to join a growing and successful team. This is a home-based and permanent role.
Key Responsibilities:
Responsible for:
- Lead the development of realistic study timelines, from design through final study reporting
Maintaining accuracy of clinical study timeline information in data control systems (e.g.,
Planisware (PPM)
- Tracking, documenting and ensuring key stakeholder involvement and timely delivery of clinical
study deliverables
- Communicating information on clinical trial status, changes, and issues to stakeholders
- Increasing the efficiency of trial operations through the sharing of cross-program knowledge and
identification of best practices leading to standardization across the organization
- Contributing to development of high performing study teams
- Participating in (or leading) special projects as assigned
- Adhering to all policies, clinical development processes, SOPs, and clinical project
management processes
- Represent CSP group in applicable forums and lead functional specific communication
Knowledge
- Drug development knowledge with understanding of other functions, including Pre-Clinical, Clinical, Development Operations, and Regulatory
- Project management tools and processes (e.g., MS Project, PPM, PowerPoint, Excel)
EDUCATION REQUIREMENTS
Basic Qualifications
- Doctorate degree
OR
- Master’s degree & 3 years of directly related experience
OR
- Bachelor’s degree & 5 years of directly related experience
OR
- Associate’s degree & 10 years of directly related experience
OR
- High school diploma / ED & 12 years of directly related experience
Preferred Qualifications
- BA/BS/BSc in the sciences or RN
- 5 years’ work experience in life sciences or medically related field, including 4 years of
biopharmaceutical clinical product development (clinical research or clinical operations
experience obtained at a biotech, pharmaceutical or CRO company)
- PMP Certification
-
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