Bilingual Pharmacist (Project Manager)

Thermo Fisher Scientific · São Paulo, Brazil

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Standing for full shift

Job Description

Join our world-class team at Thermo Fisher Scientific Inc. as a Clinical Trials Project Manager II in the State of São Paulo! This is an outstanding opportunity to contribute to groundbreaking clinical research and ensure flawless execution of projects.

Key Responsibilities

  • Advise clients on clinical investigation logistics, providing the best solutions tailored to their needs.

  • Understand and communicate logistic service capacities to clients, ensuring up-to-date knowledge of services.

  • Develop and assess project budgets, grasp project scopes, and aid in contract preparation.

  • Support client proposals through phone conferences and meetings.

  • Manage logistic projects of low to medium complexity, strategizing and problem-solving with supervisor support.

  • Act as primary liaison with clients to ensure efficient communication and compliance with project requirements.

  • Identify project needs, implement client requirements, and manage daily activities.

  • Prepare and review project documentation, ensuring tools and documents are standardized as needed.

  • Develop project startup instructions and maintain system setups.

  • Ensure accurate invoicing for services budgeted and hired in each project.

  • Contribute to financial and logistic predictions for active and new projects, providing metrics analysis.

  • Collaborate with local and foreign clients to review study requirements, discuss logistics, and support regulatory compliance.

  • Monitor and control client services, ensuring the provision of necessary reports and metrics.

  • Train project teams and operations staff according to project needs.

  • Serve as the system Subject Matter Expert (SME).

Attributes

  • Proactive problem solver with flexibility and resilience

  • Organized, committed, and attentive to client requirements

  • Strong teamwork, leadership, and interpersonal skills

  • Excellent communication and decision-making abilities

Minimum Requirements / Qualifications

  • Pharmaceutical Degree-Required
  • Experience in Clinical Trials (2-3 years)- Preferred
  • Advanced English proficiency - Required
  • Project Management experience with multiple projects (1-3 years)
  • Strong organizational and time management skills.
  • Knowledge of GMP rules, bio-security, local regulations, and SOPs
  • Skills to handle and manage multiple tasks and times with multidisciplinary teams.
  • Proactive approach to problem-solving and decision-making.
  • Strong understanding of data integrity principles and practices.

Apply now to be part of our ambitious team and help us achieve outstanding results!

Apply →