Director, Medical Writing
il y a 4 semaines
**Site Name**: Belgium-Wavre
**Posted Date**: Jan 10 2023
**Director, Medical Writing**:
**Key Responsibilities include, but are not limited to**:
**Leadership and Expertise**:
- Team leader and expert medical writing consultant.
- Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset(s) to deliver medical writing portfolio.
- Drive medical writing strategy to ensure alignment with the portfolio strategy (e.g. prioritization, acceleration, meeting upper quartile performance).
- Lead matrix team to drive the delivery of high quality, fit-for-purpose clinical documents that accurately reflect associated data and are in line with GSK standards and global/regional/local regulatory requirements, while demonstrating high performance standards for own work and encouraging similar standards across the matrix teams.
- Lead, drive, promote and implement key organizational process improvement initiatives. Proactively generate ideas for simplification and improvement taking advantage of opportunities that arise. Promote environment for others to generate ideas for improvement (e.g., continuously challenge the status quo) and champion novel business solutions in technology and ways of working.
- Lead development of training materials for a range of clinical documents. Provide mentoring, coaching and/or training to individuals or teams to develop others and shared learnings.
- Promote leadership behaviours that support GSK values.
- Provide resourcing information to TA Head to contribute to budget forecast with early escalation of risks and opportunities to ensure optimal resource utilization.
**Matrix Teamwork and Function**:
- Contribute to asset development teams and project teams as needed to ensure Medical Writing strategy is communicated and discussed
- Establish quality, efficiency, and effective teamwork across all document teams.
- Work closely with submission leads to provide significant contribution to complex clinical submission documents, document strategy and on time, efficient document delivery.
- Proven track record in writing clinical documents in scope.
**Relationship, Influence and Communication**:
- Build interactive relationships with team leaders and senior stakeholders.
- Demonstrate an outstanding track record of leading and influencing teams in a matrix environment. Promote team effectiveness across assigned projects. Build and maintain networks at project
- Departmental and inter-departmental levels; ensure timely dissemination of information to appropriate levels to improve transparency and shared learnings.
- Possess highly effective communication skills. Capable of clearly presenting ideas and data to a group, including key stakeholders at senior level or external formats.
- Motivate, influence, and advocate for medical writers, team members and senior stakeholders to effectively contribute to and review documents.
- Promote a culture of open and honest conversations, smart risk taking, decision-making, and pushing the performance edge within Medical Writing and in cross-functional platforms.
- Highly pragmatic with strong negotiation skills (to propose creative solutions to new challenges)
**Planning, Organisation and Team Coordination**:
- Able to develop and implement study and above-study document and resourcing strategies to meet project team objectives and anticipated deliverables.
- Able to develop a resourcing plan to enable efficient and accelerated delivery of documents and submissions
- Flexibility to adjust plans when project timings change particularly for complex submissions.
**Process Improvement and Compliance**:
- Lead process improvement, training, quality and compliance through ideas, proactive action, and engagement in the matrix team.
**Third-Party Resourcing Oversight**:
- Lead external resourcing and CRO interactions for project resourcing agreements.
- Implement third party resourcing agreements and oversee contract medical writers for document delivery.
- Identify need for external resource support and negotiate timelines with external medical writing vendors/CROs.
**_ Why You?_**
**Requi**red** **Qualifications**:
- We are looking for professionals with these required skills to achieve our goals:_
- PhD or relevant working experience within the life sciences space.
- Extensive experience in clinical regulatory writing experience in the pharmaceutical industry, and demonstration of leadership.
- Demonstrate experience in multicultural settings (to reflect our external customers/clients [health authorities/patients] and diverse environments with respect to dynamics of human interaction (including working with remote teams)
**Preferred Qualifications**:
- If you have the following characteristics, it would be a plus_ _:_
- Ability to lead and drive change within matrix team
- Being open to innovative medical writing solutions and driving the implementation in the ass
Nous avons d'autres emplois actuels liés à ce domaine que vous pouvez trouver ci-dessous
-
Director, Medical Writing
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-WavrePosted Date: Jan Director, Medical Writing:Key Responsibilities include, but are not limited to:Leadership and Expertise: Team leader and expert medical writing consultant. Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset(s) to deliver medical...
-
Associate Director of Medical Writing
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Maryland - Rockville, Bangalore, Belgium-Wavre, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence **Posted Date**: Jul 25 2023 Are you energized by a medical writing role that allows you to shape operational strategy and accelerate product approvals? If so, this Associate Director Medical Writing Asset Lead role...
-
Associate Director of Medical Writing
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: USA - Maryland - Rockville, Bangalore, Belgium-Wavre, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper ProvidencePosted Date: Jul Are you energized by a medical writing role that allows you to shape operational strategy and accelerate product approvals? If so, this Associate Director Medical Writing Asset Lead role could be an exciting...
-
Medical Writing Director/asset Lead
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - Brentford, Belgium-Wavre, Canada - Ontario - Mississauga, Italy - Siena, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence **Posted Date**: Jun 9 2023 **Medical Writing Director/Asset Lead** Are you interested in a highly visible, impactful position that allows you to contribute to the delivery of the GSK...
-
Associate Director Medical Writing Asset Lead
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: USA - Maryland - Rockville, Bangalore, Belgium-Wavre, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence **Posted Date**: Jun 1 2023 Are you energized by a scientific writing role that allows you to shape operational strategy and accelerate compliance? If so, this Associate Director Medical Writing and Asset Lead role...
-
Medical Writing Director/asset Lead
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: UK - London - Brentford, Belgium-Wavre, Canada - Ontario - Mississauga, Italy - Siena, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper ProvidencePosted Date: Jun 9 2023Medical Writing Director/Asset LeadAre you interested in a highly visible, impactful position that allows you to contribute to the delivery of the GSK respiratory product...
-
Associate Director Medical Writing Asset Lead
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: USA - Maryland - Rockville, Bangalore, Belgium-Wavre, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper ProvidencePosted Date: Jun 1 2023Are you energized by a scientific writing role that allows you to shape operational strategy and accelerate compliance? If so, this Associate Director Medical Writing and Asset Lead role could be an...
-
Associate Director, Medical Writing Asset Lead
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, Italy - Siena, Mississauga, UK - Hertfordshire - Stevenage **Posted Date**: Jun 9 2023 **Job purpose**: **Your responsibilities**: **Leadership and Expertise**: - Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset (s)to deliver MW...
-
Associate Director, Medical Writing Asset Lead
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-Wavre, Italy - Siena, Mississauga, UK - Hertfordshire - StevenagePosted Date: Jun 9 2023Job purpose:Your responsibilities:Leadership and Expertise: Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset (s)to deliver MW portfolio. Lead matrix team to...
-
Associate Director, Scientific Writing
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, Bengaluru Luxor North Tower, Italy - Siena, UK - London - Brentford, USA - Pennsylvania - Upper Providence **Posted Date**: Mar 13 2023 **Job purpose**: **Your responsibilities**: **Leadership and Expertise**: - Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising...
-
Associate Director, Scientific Writing
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-Wavre, Bengaluru Luxor North Tower, Italy - Siena, UK - London - Brentford, USA - Pennsylvania - Upper ProvidencePosted Date: Mar Job purpose:Your responsibilities:Leadership and Expertise: Lead one or more assets and serve as a medical writing point of contact for this/these assets. Support prioritising workload across an asset (s)to...
-
Medical Project Director
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-Wavre, UK - London - BrentfordPosted Date: May 3 2023Medical Project Director:We currently have an exciting opportunity to work in a fast paced, high performing Medical Affairs team as a Medical Project Director, reporting into the Head of Project Management. This is a critical role which will be responsible for leading and developing a...
-
Medical Director, Global Medical Affairs
Il y a 2 mois
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, Cambridge MA, Upper Providence, USA - Massachusetts - Cambridge, USA - Pennsylvania - Upper Providence **Posted Date**: Jan 16 2023 Are you interested in a highly visible Medical Affairs role that allows you to be ambitious for patients and contribute to the advancement of novel vaccines with the potential for substantive...
-
Medical Director, Global Medical Affairs
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-Wavre, Cambridge MA, Upper Providence, USA - Massachusetts - Cambridge, USA - Pennsylvania - Upper ProvidencePosted Date: Jan Are you interested in a highly visible Medical Affairs role that allows you to be ambitious for patients and contribute to the advancement of novel vaccines with the potential for substantive public health impact?...
-
Global Medical Affairs Director, Shingrix
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, GSK House, UK - Hertfordshire - Stevenage **Posted Date**: Feb 16 2023 **Global Medical Affairs Director, Shingrix** Are you interested in a highly visible medical affairs leadership role that allows you to design and lead the strategic direction for our vaccines in order to protect the lives of millions of patients around...
-
Global Medical Affairs Director, Shingrix
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Belgium-Wavre, GSK House, UK - Hertfordshire - StevenagePosted Date: Feb Global Medical Affairs Director, ShingrixAre you interested in a highly visible medical affairs leadership role that allows you to design and lead the strategic direction for our vaccines in order to protect the lives of millions of patients around the world? If so, this...
-
Director Strategic Resourcing
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Bengaluru Luxor North Tower, Belgium-Wavre, Canada - Ontario - London, Canada - Ontario - Mississauga, Italy - Siena, Upper Providence, USA - Maryland - RockvillePosted Date: Jun Are you looking for a leadership role that allows you to shape and accelerate scientific communications and enhance the medical writing process? If so, this Scientific &...
-
Director, Global Medical Affairs Lead
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: Belgium-Wavre, GSK Tres Cantos, Madrid, Italy - Siena, UK - London - Brentford **Posted Date**: May 10 2023 **Director/Senior Director Global Medical Affairs Lead - Scientific Affairs & Public Health, Global Health Access**: Are you motivated by GSK’s Global Health ambition to reduce health inequalities by changing the trajectory of high...
-
Serm Associate Medical Director
il y a 1 semaine
Wavre, Wallonie, Belgique GSK Temps pleinSite Name: Warsaw Cirrus, Belgium-Wavre, Bengaluru Luxor North TowerPosted Date: Jul 5 2023SERM Associate Director / for VCSP:Safety Evaluation and Risk Management Associate Director for VCSP (Vaccine Clinical Safety and Pharmacovigilance):You will actively manage and evaluate risks associated with assigned vaccine projects, and make recommendations for the...
-
Director, Senior Director
il y a 3 semaines
Wavre, Belgique GSK Temps plein**Site Name**: UK - London - Brentford, Belgium-Wavre, Warsaw **Posted Date**: Feb 13 2024 **Director/Senior Director/Executive Director**: **Safety Physician, Medical Director (Safety, Evaluation & Risk Management)**: Our Safety Physician provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in...
