Pharmaceutical Development Project Manager at PROMED Pharmaceutical Company
PROMED pharmaceutical company is looking for a Pharmaceutical Development Project Manager
Responsibilities:
- Preparation and updating of project roadmaps, monitoring the execution of key project stages
- Preparation and updating of project schedules, task execution monitoring
- Participation in the organization of planning and monitoring of project budget compliance
- Interaction with cross-functional departments, building effective communication within the project team, resolving problem cases during project work
- Informing the project team about the project status, critical project changes
- Organizing meetings, preparing meeting summaries for product projects
- Preparation of project reporting presentations for TOP management, as well as presentations on specific topics within the scope of expertise
- Ensuring interaction with contract organizations, discussing contract terms with the project team
- Participation in the preparation, maintenance, and management of project documentation, including the preparation and collection of the registration dossier
- Participation in the development of quality management system documents regarding project management (policies, etc.)
- Identification of project implementation risks and development of measures for their minimization
- Participation in the development of an information system for recording and tracking task completion
- Participation in the organization of pharmaceutical development and establishment of key project results with management
- Participation in the organization of product project expertise
- Mentoring junior staff of the project management department in their area of responsibility/expertise
- Leading transfer projects, conducting expertise of potential partners' documentation, coordinating transfer processes (internal and external)
Requirements:
- Ability to effectively allocate resources, plan and monitor task execution, meet deadlines
- Ability to clearly and understandably communicate information to colleagues and management
- Ability to implement new methods to improve processes
- Ability to assess risks and develop strategies for their minimization
- Ability to prepare reports, technical documentation, and sections of the registration dossier
- Knowledge of regulatory requirements, including GMP, Resolution No. 89, and other regulatory standards
- Results-oriented
- Responsibility, stress resistance, efficiency, initiative
- Required English level B1
- Proficiency in specific software: MS Project, 1C, Advanta, Excel, Power Point
Working Conditions:
- Official employment, indefinite employment contract
- Transparent salary (discuss your expectations by phone)
- Working hours Mon-Fri, 9 AM - 6 PM, office-based work
- Social package: Voluntary Medical Insurance (DMS) with a good selection of clinics and dentistry
- Mobile communication
- Management with a Western approach and standards
