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Project Manager

2 meses atrás

Porto Velho, Rondônia, Brasil Signant Health Tempo inteiro
About the Role

We are seeking a highly skilled Project Manager to join our team at Signant Health. As a Project Manager, you will be responsible for the planning, execution, and completion of projects within the clinical trials and pharmaceutical industry.

Key Responsibilities
  • Manage and lead project delivery tasks, including software development lifecycle (SDLC) of Simple to Medium complexity studies.
  • Ensure project systems are built and released in accordance with client expectations, including leading the project system change control process.
  • Support the implementation of complex, multi-product projects as needed.
  • Manage projects in accordance with established timelines, budget, quality standards, and/or contractual requirements.
  • Review, approve, and maintain project and corporate systems and documentation.
  • Handle client escalations independently and work with internal and client teams to resolve.
  • Take responsibility for the quality of communication with clients, including cadence, content, and audience.
  • Account for the financial health of assigned projects, including vendor services, licensing, payments, invoicing, devices, resource assignments, and vendor management activities.
  • Collaborate with other functional areas for project delivery to ensure timelines and client expectations are met within budget.
  • Responsible for identifying and documenting Incident Reports with the Quality Management group, including client notification and closure.
  • Responsible for reporting project status updates.
Requirements
  • Bachelor's degree or equivalent or relevant experience.
  • Understanding of the software development life cycle and the specification and configuration of software products.
  • Ability to multi-task and work with multiple team members.
  • Excellent time management, communication (oral and written), and organizational skills.
  • Attention to detail and first-time quality delivery orientation.
  • Solid MS Office Suite experience, including Word, Excel, MS Project, and PowerPoint.
  • Ability and experience in direct project activities and ensuring customer satisfaction while understanding and adhering to the study budget.
  • Ability to communicate and engage effectively with all levels of the organization and have excellent written and spoken English skills.
  • Experience in a Project Management role or equivalent.
  • Initiative and ability to work independently as needed.
Preferred Qualifications
  • Background in Pharmaceutical, Medical education, and/or CRO.
  • Experience in the clinical trials/pharmaceutical industry/life sciences.
  • Ability to travel for business trips (overnight business trips could be expected quarterly).
  • Experience/understanding of the clinical research environment and GCP principles.
  • PMP or equivalent certificate.
About Signant Health

Signant Health is a high-growth, dynamic company in the clinical trials industry. We are committed to creating a culture of process improvement, streamlining our processes to add value to our business and meet client needs.

We are looking for individuals who are excited by the potential to make a difference in the world. You don't need to have a clinical background to thrive at Signant. You need to be decisive, open to celebrating mistakes, able to communicate transparently and inclusively, and someone your team can count on.