Pharmaceutical Development Project Manager

We are PROMOMED Group of Companies, an innovative Russian pharmaceutical company engaged in the production and promotion of prescription and over–the-counter drugs in several therapeutic areas: endocrinology, infectious diseases, rheumatology, neurology, urology, cardiology, gynecology and others.

The main asset of the Promomed Group is its employees.
One of our values, cooperation and development, reflects the culture and atmosphere in the company.
We value openness to new things, support those who want to learn, and we sincerely believe in what we do.

We invite you to join our team as a Pharmaceutical Development Project Manager.

Responsibilities

• Preparation and updating of project roadmaps, monitoring the implementation of key project milestones
• Preparation and updating of project schedules, monitoring of tasks
• Participation in the organization of planning and monitoring of compliance with the project budget
• Interaction with cross-functional departments, building effective communication within the project team, solving problematic cases in the process of working on the project
• Informing the project team about the status of the project, critical project changes
• Organization of meetings, preparation of summaries of meetings on product projects
• Preparation of reporting presentations on projects for TOP management, as well as presentations on a given topic within the framework of expertise
• Ensuring interaction with contract organizations, discussing the terms of contracts with the project team
• Participation in the preparation, maintenance and management of project documentation, including the preparation and collection of registration dossier
• Participation in the development of quality management system documents related to project management (policies, etc.)
• Identification of project implementation risks and development of measures to minimize them
• Participation in the development of an information system for accounting and tracking the completion of tasks
• Participation in the organization of pharmaceutical development and the establishment of key project results with management
• Participation in the organization of the examination of product projects
• Mentoring the work of the junior staff of the project management service in the field of their functionality/expertise
• Leadership of transfer projects, examination of documentation of potential partners, coordination of transfer processes (internal and external)

Requirements

• The ability to effectively allocate resources, plan and monitor the completion of tasks, and meet deadlines
• The ability to communicate information clearly and clearly to colleagues and management
• The ability to implement new methods to improve processes
• The ability to assess risks and develop strategies to minimize them
• Ability to prepare reports, technical documentation and sections of the registration dossier
• Knowledge of regulatory requirements, including GMP, Decision No. 89 and other regulatory standards
• Result orientation
• Responsibility, stress tolerance, efficiency, initiative
• Required English level B1
• Proficiency in certain software: MS Project, 1C, Advanta, Excel, Power Point

Working conditions

• Official registration in the state, indefinite employment contract
• White salary (we will discuss your wishes by phone)
• Opening hours Mon-Fri, 9-18, office work
• Social package: VMI with a good selection of clinics and dentistry
• Mobile communication
• A guide with a Western approach and standards

If you want to become part of our team, send your resume indicating your salary expectations