When our values align, there's no limit to what we can achieve. We are currently looking for a Senior Regulatory Affairs Consultant (Project Lead)! As a Senior Consultant you will be responsible for leading internal projects on behalf of Parexel Clients.
A Senior Consultant provides a broad range of consulting services and works within project guidelines to identify, refine, and address client issues and to achieve project objectives.
We are looking for an experienced candidate with strong organizational skills, the ability to prioritise and influence internal teams, as well as developing client relationships.
You will provide guidance to project team members on technical/process issues.
In this role you will have solid EU regulatory experience (predominantly for post approval submissions for mature products portfolios).
The role can be home or office based in various European locations.
Job Responsibilities: Project Initiation Management: Own the client relationship and responsibility for client communication ensuring high client satisfaction Cooperates with the Finance Business Partner to ensure that any systems and system interfaces are functioning Work with RAL Regulatory Affairs Lead and /or TL Technical Lead to provide initial schedule and resource plan to Global Resourcing Team GRTPro-active approach to providing solution set for clients Project Execution Management: Lead client kick off meeting and discussions with client, establishing client expectations for project delivery, communication, and client specific metrics.
Ensure the scope of the project is well understood by the project team and set the team expectations Project Implementation, Control & Evaluation: Manage the project such that it is completed within budget, schedule and according to contract specifications Ensure the project is progressing according to quality standards, SOPs, and to fulfil local regulations Proactively take action where required to maintain project deliverables, to effectively manage the project’s critical path, resourcing, metrics compliance, the budget and third party vendors Manage the project budget with the Finance Business Partner including the completion of monthly revenue recognition, forecasting and cost management Project Closure Management: Oversee all administrative closeout procedures are completed, according to Project Closeout Checklist Review the project contract exhibit and ensure relevant team members have received it Manage the set-up of the project team, oversee request for resources, review proposed team members for suitability and manage any project team changes throughout the duration of the project.
Review initial budget request with SC/CXD Program Director for any project specific adaptations Participate in or manage the team kick-off meeting Skills and Experience required for the role: University Degree in a Scientific or Technical Discipline, Advanced Degree Preferred PMP or equivalent - nice to have Extensive years of Regulatory Affairs experience in an industry-related environment CRO experience Experience in MAA & Lifecycle maintenance activities preparation and submissions Project management knowledge and experience Financial management skills Excellent interpersonal and intercultural communication skills, both written and verbal Fluent in English
reklama
Regulatory Affairs Project Lead (maas), Prague
Free
Regulatory Affairs Project Lead (maas), Prague
Czech Republic, Prague, Prague,
Publikováno November 29, 2024
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PAREXEL International is a leading global biopharmaceutical services provider, which continues to be a premier, trusted partner to clients who rely on the Company for expertise and flexibility, as well as the efficiencies of a worldwide infrastructure, to help them more quickly achieve their development and commercialization goals. For 30 years, PAREXEL has complemented client organizations with strategic insight, deep scientific knowledge, tactical expertise, and a wealth of experience throughout the development process. The Company's offerings include worldwide regulatory expertise, Phase I-IV clinical research services, eClinical technologies that accelerate development, and integrated commercialization services. PAREXEL is focused on providing tailored solutions that match a client's specific needs by applying the right blend of resources and capabilities, as well as the right guidance and high level of quality needed to help them bring safe and effective treatments to patients sooner.
Headquartered near Boston, Massachusetts, PAREXEL operates in over 70 locations throughout more than 50 countries, and has over 11,000 employees worldwide.
Visit www.PAREXEL.com for more information.
Specialties
Regulatory and product development consulting,
early phase clinical research,
phase II-III clinical research,
late phase clinical research,
eClinical solutions,
patient and site recruitment,
clinical logistics,
flexible outsourcing models,
strategic partnering