Lavori attuali relativi a Director Medical Writing Submission Facilitator - Siena - GSK
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Siena, Italia GSK A tempo pieno**Site Name**: Belgium-Wavre, Italy - Siena **Posted Date**: Sep 6 2024 **_ Job purpose:_** ***: **Are you looking for a highly visible medical writing role that broadens your project management capabilities? If so, this Medical Writing Asset Lead role could be an ideal opportunity to consider.**: ***: **As a Medical Writing Asset Lead, you will lead...
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Director Medical Writing Submission Facilitator
3 mesi fa
**Site Name**: Wavre, Italy - Siena, Mississauga
**Posted Date**: Aug 30 2024
GSK has an inspiring ambition: by uniting science, technology and talent we aim to positively impact the health of 2.5 billion people over the next ten years. We will get ahead of disease together with our R&D approach of focusing on the science of the immune system, human genetics and advanced technologies, such as functional genomics and AI/ML.
**Job Purpose**:
**Key Responsibilities**:
- Partners with the MW LT and MW Submission leads in developing, driving, implementing and embedding accelerations levers in a multi-cultural, cross-functional, and cross
- Therapy Area setting including senior stakeholders.
- Be a change champion and strong advocate for embedding and utilizing Acceleration Levers and relevant Hyper Acceleration technology in the hyper-acceleration ambition submission teams in a multi-cultural, cross-functional, and cross Therapy Area setting including senior stakeholders.
- Leads, drives and promotes MW acceleration strategy and represents MW in hyper-acceleration ambition submission forums such as the Acceleration Squad Meetings.
- Proactively generates ideas for simplification and improvement in the area of hyper-acceleration ambition submissions.
- Builds interactive relationships with Functional leads and senior stakeholders in the context of acceleration.
- Removes blockers to hyper-acceleration ambition submission acceleration and escalates issues.
- Ensures relevant stakeholder management in close collaboration with the MW Head, MW Head of H&E and Medical Writing TA Heads.
- Highly pragmatic with strong negotiation skills.
- Facilitates execution of agreed timelines for the clinical submission document within the remit of Medical Writing in close collaboration with the Medical Writing Submission Lead and Submission Medical Writer Lead Authors.
- Promotes agility in ways of working within submission teams.
- Ensures submission teams are trained in the MW owned acceleration levers and Hyper Acceleration technology.
- Ability to oversee and support multiple hyper-acceleration ambition submission teams in parallel.
**Basic Qualifications**:
- PhD degree in Life Science/ Health Science or equivalent.
- Extensive years of experience in clinical submissions dossier work as an SME - corresponding to Director/Program Lead - in a global Pharma R&D or CRO setting with a profound understanding of the clinical development process and phases of development.
- Demonstrated influential skills in a fast-paced, high-pressure multi-cultural environment.
- Track-record of delivering business outcomes and value and simplification with a passion for science and advancing medicines to patients
- Experience in multicultural settings, diverse environments with respect to dynamics of human interaction.
- Excellent strategic, planning and organizational skills.
- Excellent interpersonal skills
- Strong problem-solving and negotiation skills
- Highly structured and diligent.
- Relentless for delivering business outcomes and value and simplification with a passion for science and advancing medicines to patients
- Excellent communication skills in verbal and written English.
**Preferred Qualifications**:
- Being able to navigate a complex matrix organisation with an ability to partner with, and influence, senior stakeholders across the company.
LI-GSK*
If you have a disability and require assistance during the course of the selection process, you will have the opportunity to let us know what specific assistance you require in order to make suitable arrangements.
**Why GSK?**
**Uniting science, technology and talent to get ahead of disease together.**
GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
**Important notice to Employment businesses/ Agencies
