As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small.
In return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. Plus, as member of Parexel Consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. Join our team, and you will design solutions for the complexities of an ever-changing global marketplace.
- Full Time
- Level: Mid
- Travel: Yes
- Glassdoor Reviews and Company Rating
Success Profile
Check out the top traits we're looking for and see if you have the right mix.
- Detail-Oriented
- Proactive
- Problem-Solver
- Results-Driven
- Organized
- Multi-Tasker
Rewards
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Global Impact
We are one truly global team working together to propel each client´s journey ahead faster.
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Balance
We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
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Collaboration
Work with industry leaders and subject matter experts.
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Freedom
The ability to innovate, ask “what if” and try new solutions without fear of failure.
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Variety
Opportunities to work on multiple accounts – never boring!
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Management
Strong management with depth of experience working for global health authorities.
Responsibilities
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 GRT
Pro-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
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