Salary
💰 $110,000 - $130,000 per year
About the role
- Develop comprehensive project plans including timelines, resource allocation, and budget management; Facilitate collaboration among cross-functional teams including R&D, Clinical Operations (CERP), Regulatory Affairs, Quality, Marketing, Manufacturing and others; Track project milestones and deliverables, identifying and mitigating risks proactively; Prepare and present project status reports to senior management and stakeholders; Ensure compliance with relevant regulatory standards; Manage external partnerships and vendor relationships critical to product development; Support the preparation of regulatory submissions and interactions with health authorities; Assist in Business Case Development of new products.
Requirements
- Bachelor's degree in Business Management, Project Management Life Science or related field; PMP certification or equivalent project management credentials desired; 2+ years of project management experience; Thorough knowledge of FDA, EMA, and related industry regulations; Experience with project management software and methodologies; Excellent communication, leadership, and stakeholder management skills; Strong problem-solving abilities and attention to detail; Experience in the Pharma industry is a plus.