Project Manager Ii In Early Phase - Sponsor Dedicated - Based In Spain/bulgaria/romania/portugal/hungary/poland/south Africa

Syneos Health

Spain
**
Gcp, sops, and regulatory compliance
Timely study launch, conduct, and closeout
Quality, timelines, and budget management
** Syneos Health is seeking a Project Manager II for early phase clinical research, with locations in several European countries and South Africa. The role involves overseeing clinical studies, ensuring compliance, managing project timelines and budgets, and fostering client relationships. **

Job Summary

  • Manages interdisciplinary clinical research studies, ensuring compliance with GCP, SOPs, and regulatory requirements, acting as the primary liaison between the Company and the Customer.
  • Leads project teams to ensure quality, timelines, and budget management, with accountability for financial performance and proactive issue management.
  • Responsible for TMF quality, maintenance of study information, inspection readiness, and development of contingency and risk mitigation strategies.

Matching Summary

Match Score: 75

** Syneos Health is seeking a Project Manager II for early phase clinical research, with locations in several European countries and South Africa. The role involves overseeing clinical studies, ensuring compliance, managing project timelines and budgets, and fostering client relationships. **

Skills & Requirements

Must-have

  • GCP, SOPs, and regulatory compliance
  • Timely study launch, conduct, and closeout
  • Quality, timelines, and budget management
  • Financial performance accountability
  • Study conduct partner coordination
  • TMF quality and completeness
  • Inspection readiness
  • Project plan development and implementation

Nice-to-have

  • Agile and driven to deliver
  • Passionate problem solvers
  • Develop strong client relationships
  • Embrace new technologies

Key Requirements

  • Bachelor’s Degree (or equivalent) in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
  • Clinical research organization (CRO) and relevant therapeutic experience preferred
  • Strong knowledge of Good Clinical Practice/ICH guidelines
  • Ability to travel as necessary (approximately 25%)

Work Rights

Not specified

Tailored Resume

Cover Letter