Project Management Officer Pmo H/F - GI Life Sciences
- Saclay - 91
- CDI
- GI Life Sciences
Les missions du poste
We are recruiting in Saclay, a Project Management Officer (PMO) H/F, for the Regulatory Business Operations Division of a French pharmaceutical group, recognised for its expertise in the research, development and marketing of medicines and health products, with a strong emphasis on innovation.Project Management Officer (PMO) H/F
Gi Group Consulting, a subsidiary of GiGroup Holding, is a consulting firm specialising in Life Sciences. We dedicate our expertise to our clients: Pharmaceutical Groups, CROs, and Biotechnology companies.
Accountable for:
- Follow-up on boarding and training plan (visa, role, access, tools, trainings...),
- Organise meetings and follow actions within different work streams,
- Define the operational planning of the implementation of the new outsourcing model including (training, procedures, KPI, governance, projects hand over, other Work stream deliverables) in collaboration with the service provider,
- Review and analyse existing operational processes in the organisation to identify problems, inefficiencies, and opportunities for improvement,
- Support operational teams to understand process needs and constraints,
- Check and make improvement on current documentation related to processes, including workflows, roles & responsibilities and procedures,
- Support implementation of performance indicators to monitor process efficiency and identify opportunities for improvement,
- Collaborate with stakeholders to implement proposed changes and ensure their adoption.
Le profil recherché
Skills:
- Excellent ability to solve problems proactively,
- Strong communication and collaboration skills with different stakeholders,
- Ability to work independently and manage multiple projects simultaneously,
- Attention to detail and quality orientation,
- Knowledge of the regulatory affairs environment.
Profile / Experience:
Project Manager with a minimum of 3 years of experience.
Experience in project management and a background in regulatory affairs would be a plus.