JMD Technologies Inc. is seeking a Senior Project Manager to oversee complex, enterprise-level initiatives within the R&D Quality function. This role focuses on improving operational efficiency and ensuring effective collaboration across clinical, research, and quality teams in highly regulated biotech or pharmaceutical environments.
Responsibilities:
- Drive planning, execution, and delivery of high-impact, cross-functional RDQA programs
- Implement structured PM methodologies to improve consistency, transparency, and execution discipline
- Design and maintain governance models, reporting cadence, risk tracking, and escalation frameworks
- Collaborate with clinical, quality, compliance, and research stakeholders to ensure strategic alignment and regulatory adherence
- Provide executive-level updates and maintain clear communication across multiple workstreams
- Analyze workflows and operational data to identify inefficiencies and implement process improvements
- Support organizational maturity through scalable systems, controls, and best practices
Requirements:
- Bachelor's degree with 10+ years of project management experience
- At least 5 years of experience within biotech, pharmaceutical, or clinical research settings
- Strong command of traditional project management principles and lifecycle governance
- Demonstrated experience building or enhancing Quality Governance structures
- Solid understanding of clinical research operations and regulatory standards (GCP required; familiarity with GVP, GMP, GDP, CMC preferred)
- Strong stakeholder engagement, facilitation, and leadership skills
- PMP or related certification (PMI, Agile, Six Sigma)