Aktuelle Jobs im Zusammenhang mit Manager/associate Director Clinical Pharmacology Lifecycle Management - Baar - GSK
-
Associate Director Fp&a International Markets
Vor 7 Tagen
Baar, Schweiz Exact Sciences Corporation Vollzeit**Help us change lives** At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re...
-
Associate Director, Field Learning
Vor 3 Tagen
Baar, Schweiz Biogen VollzeitA leading biotechnology company in Zug, Switzerland is seeking an Associate Director, Field Commercial Training Partner. In this role, you will develop and implement learning strategies to enhance commercial team performance. The ideal candidate has over 10 years of experience in Learning within the pharmaceuticals, excellent stakeholder management...
-
Director, Portfolio Strategy
vor 2 Wochen
Baar, Zug, Schweiz Novocure VollzeitAt Novocure, we are pioneering Tumor Treating Fields (TTFields) – a non-invasive cancer therapy designed to disrupt tumor cell division and extend survival in some of the most aggressive forms of cancer. Every role here contributes to improving the lives of people living with cancer.We are seeking aDirector of Portfolio Strategybased in Baar, Switzerland,...
-
Associate Director, Global Oncology Training
Vor 4 Tagen
Baar, Schweiz AstraZeneca VollzeitBe part of fulfilling our ambition to be world leaders in Oncology. We are already the fastest growing team within AstraZeneca and across the industry, and there are countless new indications and targets in our game-changing pipeline. We deliver this value through launch excellence, commercial effectiveness and maximising the lifecycle. By leveraging our...
-
Global Medical Director, Oncology
vor 1 Woche
Baar, Schweiz GSK Vollzeit**Site Name**: Baar Onyx, Belgium-Wavre, GSK HQ, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence **Posted Date**: Feb 26 2025 - Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you! _ **Medical...
-
Director, Portfolio Strategy
vor 2 Wochen
Baar, Zug, Schweiz Novocure VollzeitAt Novocure, we are pioneering Tumor Treating Fields (TTFields) – a non-invasive cancer therapy designed to disrupt tumor cell division and extend survival in some of the most aggressive forms of cancer. Every role here contributes to improving the lives of people living with cancer.We are seeking aDirector of Portfolio Strategybased in Wayne,...
-
Associate Director, Global Regulatory Strategy
vor 9 Stunden
Baar, Zug, Schweiz Biogen VollzeitAbout This RoleThe Associate Director, Global Regulatory Strategy will be responsible for developing and delivering innovative, breakthrough global and EU regulatory strategies for product development and approval, in alignment with the global business strategy. Responsibility of leading the global and EU regulatory strategy for the development of their...
-
Global Medical Director, Gma Oncology
vor 2 Wochen
Baar, Schweiz GSK VollzeitThe **Global Medical Director, GMA Oncology** role is a unique opportunity for an experienced, innovative, and proactive medical professional to facilitate the understanding of the value of our oncology medicines, the science behind them and the public impact they can offer. This is accomplished by developing and implementing the global medical scientific...
-
Associate Director, Business Operations
vor 2 Wochen
Baar, Zug, Schweiz Biogen VollzeitAbout This Role:As the Associate Director of Business Operations & Performance for Region EU, you will be a pivotal member of our dynamic team, enabling and supporting regional efforts to optimize stakeholder collaboration and drive performance management commitments. In this operations-focused role, you will manage strategic insights and operational...
-
Associate Director Global Medical Training
vor 1 Woche
Baar, Zug, Schweiz Biogen VollzeitAbout This Role:As the Associate Director of Global Field Medical Training and Excellence, you will play a pivotal role within the Global Medical Capability team. Tasked with creating a sustainable learning strategy for Biogen's Regional and Global field medical teams, you will ensure alignment with the company's overarching medical strategy. You will serve...
Manager/associate Director Clinical Pharmacology Lifecycle Management
vor 2 Wochen
**Site Name**: UK - London - New Oxford Street, Baar Onyx, Home Worker - GBR, Upper Providence, Wavre
**Posted Date**: Feb 19 2025
**415150 Manager/Associate Director, Clinical Pharmacology (Lifecycle Management) - 2 Year Fixed Term Contract/Secondment**
Are you energized by a role that requires strategic thinking and extensive internal and external engagement? If so, this Manager/Associate Director Clinical Pharmacology Lifecycle Management role could be an exciting opportunity to explore.
The Manager/Associate Director Clinical Pharmacology Lifecycle Management will provide clinical pharmacology, therapeutic and regulatory support for GSK’s product portfolio worldwide. The individual will also contribute to the evidence generation plans for new and existing medicinal products.
We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme.
We embrace modern work practises; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.
Discover more about our company wide benefits and life at GSK on our webpage _Life at GSK | GSK_
**In this role you will**
- Ensure integration of clinical pharmacology and PKPD principles into clinical development, regulatory approval and life-cycle management of GSK products.
- Support accelerated regulatory filing activities across multiple regions/markets, with focus on country-specific requirements.
- Lead the preparation, authoring and review of CTD modules taking into account country-specific regulatory requirements for effective submissions and approval of new products, indications and/or relevant label extensions.
- Develop and maintain a strong working knowledge of pharmacology, physiology, clinical pharmacology, therapeutics, and statistics, such that adequate expertise and support is provided to business partners and project teams
- With appropriate guidance contribute to the design, data analysis, interpretation and reporting of clinical pharmacology studies.
- With appropriate guidance implement, analyse and report PK, PKPD, and drug-disease modelling and simulation studies.
**_ Why you?_**
**Basic Qualifications & Skills**:
**We are looking for professionals with these required skills to achieve our goals**:
- PhD and/or MD degree in clinical pharmacology or other relevant discipline (e.g. Pharmaceutical Sciences, Bioengineering, Pharmacy)
- Understanding of regulatory guidelines, ideally demonstrated experience interacting with regulatory authorities
- Project management experience
**Preferred Qualifications & Skills**:
**Please note the following skills are not necessary, just preferred, if you do not have them, please still apply**:
- Knowledge of pharmacology, physiology, clinical pharmacology, biopharmaceutics, regulatory affairs, therapeutics and commercialization such that he/she can assist in managing these interfaces and promote a strong partnership with Medical Affairs, Clinical Safety and other relevant business partners.
- Experience in the design, analysis, interpretation and reporting of clinical pharmacology studies, including bioequivalence, concentration-QT, drug-drug interaction, organ impairment, and other special populations (e.g. Japanese, older adults)
- Working knowledge in standard and innovative clinical study protocol design across different phases of development and life-cycle management, including evaluation of real-world evidence
- Experience in quantitative clinical pharmacology, including population PK modelling, drug-disease modelling, clinical trial simulations, and dosing algorithms
- Understanding of statistical methodologies: hypothesis testing, Bayesian inference, nonlinear mixed-effects modelling
- Proven performance in a matrix team environment
**Closing Date for Applications - March 10th, 2025 (COB)**
Please take a copy of the Job Description, as this will not be available post closure of the advert.
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong tech-enabled capabilities that allow us to build a deeper understanding of the patient, human biology and disease mechanisms, and transform medical discovery. We are revolutionising the way we do R&D. We’re uniting science, technology and talent to get ahead of disease together.
Find out more:
Our approach to R&D.
**Why GSK?**
**Uniting science, technology and talent to get ahead of disease together.**
GSK is a global biopharma company with a special purpose - to u
