Aktuelle Jobs im Zusammenhang mit Medical Director - Zug - GSK
-
Global Medical Director- Blenrep
vor 1 Woche
Zug, Schweiz GSK Vollzeit**Site Name**: Home Worker - USA, GSK House, Zug House **Posted Date**: Dec 11 2024 The Global Medical Director role is a unique opportunity for an experienced, innovative, and proactive medical professional to facilitate the understanding of the value of our medicines and vaccines, the science behind them and the public impact they can offer. This is...
-
Medical Director, Oncology Clinical Development
vor 22 Stunden
Zug, Schweiz GSK Vollzeit**Site Name**: UK - London - New Oxford Street, Stevenage, Switzerland - Zug, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence, Warsaw **Posted Date**: Nov 21 2024 MEDICAL DIRECTOR- ONCOLOGY CLINICAL DEVELOPMENT Are you looking to join an ambitious oncology clinical development organisation, focusing on the development of ADCs in the GI...
-
Medical Director, Oncology Clinical Development
Vor 6 Tagen
Zug, Schweiz 1925 GlaxoSmithKline LLC VollzeitAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients,...
-
Medical Director, Oncology Clinical Development
vor 1 Woche
Zug, Schweiz 1925 GlaxoSmithKline LLC VollzeitAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients,...
-
Director Global Quality
vor 1 Woche
Zug, Schweiz SHL Medical AG Vollzeit**Job Overview** The position of the Director global Quality of SHL Medical AG holds overall responsibility for compliance to all applicable regulations pertaining to all operations functioning on the assigned site as well as corporate compliance to all applicable regulations including cGMP pertaining to all the markets currently being served by the...
-
Costumer Solutions Regional Director, Europe
Vor 3 Tagen
Zug, Schweiz SHL Medical AG Vollzeit**Location**:Zug, Switzerland **Reporting to**:Head of Portfolio Strategy & Customer solutions SHL Medical is the world-leading solution provider in the design, development, and manufacturing of advanced drug delivery systems with more than 5000 employees worldwide. Our customers include top pharmaceutical and biotech companies from around the globe that...
-
Medical Affairs Lead Oncology
vor 1 Woche
Zug, Schweiz Johnson & Johnson Vollzeit**Job Function**: Medical Affairs Group **Job Sub Function**: Medical Affairs **Job Category**: People Leader **All Job Posting Locations**: Zug, Switzerland **About Oncology** Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by...
-
Medical Affairs Lead Oncology
Vor 5 Tagen
Zug, Schweiz Johnson & Johnson Vollzeit**Function** - Medical Affairs Group **Sub function** - Medical Affairs **Category** - Senior Manager, Medical Affairs (PL8) **Location** - Zug / Switzerland **Date posted** - Jun 25 2025 **Requisition number** - R-020421 **Work pattern** - Hybrid Work Description **Job Function**: Medical Affairs Group ** Job Sub Function**: Medical Affairs ** Job...
-
Medical Science Liaison Rare Tumors Switzerland
Vor 5 Tagen
Zug, Zug, Schweiz The businesses of Merck KGaA, Darmstadt, Germany VollzeitSpringWorks Therapeutics, a healthcare company of Merck KGaA, Darmstadt, Germany, is a commercial-stage biopharmaceutical company dedicated to improving the lives of patients with rare tumors. We developed and are commercializing the first and only FDA and EC approved medicine for adults with desmoid tumors and the first and only FDA and EC approved...
-
Zug, Zug, Schweiz Merck Healthcare VollzeitWork Your Magic with usReady to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of...
Medical Director
vor 3 Wochen
**Site Name**: USA - Pennsylvania - Upper Providence, GSK HQ, Switzerland - Zug, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham, Warsaw Rzymowskiego 53
**Posted Date**: Feb 21 2025
Medical Director - Oncology Clinical Development - Hematology-Oncology
The Medical Director Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK’s clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders so as to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts.
This position will support our growing oncology portfolio for the treatment of hematological malignancies. The Medical Director will have the opportunity to work across early
- to late-stage development and in partnership with a multi-disciplinary team of oncology drug developers.
An on-site office presence for a minimum of two days a week is required in one of GSK’s UK (London or Stevenage), US (PA or MA), Switzerland (Zug) or Poland (Warsaw) campuses.
**Key Responsibilities**
- Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex matrix environment to develop and execute phase 1-3 interventional clinical trials
- Ensure high quality protocol development aligned with the Clinical Development Plan to effectively determine a medicine’s potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe.
- Use medical expertise to contribute to the end to end (protocol concept to final study report) to ensure scientific integrity and timely delivery of clinical trials which ensure consistency with the clinical development strategy for regulatory approvals, reimbursable medicines, and successful lifecycle management; demonstrate ability to incorporate global considerations into decision making
- Interpret and summarize study results consistent with objectives to define safety, efficacy, pharmacokinetic/pharmacodynamic, and patient reported outcomes, and applicability of data to the targeted patient population.
- Assume medical responsibility for clinical trials with active participation in real-time medical monitoring of studies, including patient eligibility assessment, study design questions, and addressing urgent safety questions (with inclusion of Safety/ PV as relevant).
- Assume responsibility for medical review of clinical trial data, both directly as needed and/or via oversight of delegated medical review. Oversee blinded review of data packages intended for IDMCs.
- Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.
- Participate in the authoring of clinical study reports and regulatory documents and collaborate with colleagues in Regulatory Affairs, CMC, Toxicology, Research, Pharmacology to respond to health authority and ethics committee queries.
- Collaborate with Principal Investigators in the evaluation and assessment of publications (abstracts, posters, manuscripts) associated with clinical data.
- Network extensively to develop long-term strategic partnerships with thought leaders both internally and externally, in support of GSK’s vision.
- Understand biological mechanisms, clinical strategy, scientific interpretation of disease and target-based literature.
- Serve as a core member of the Clinical Matrix Team for one or more assets in development.
- Represent Clinical Development on disease area strategy, integrated evidence and medical affairs strategy teams.
- Participate in Oncology Clinical Development-wide initiatives and workstreams as appropriate.
Basic Qualifications Include:
- Medical degree (MD, MD/PhD, or equivalent) with board certification/eligibility or registration qualifications in medical oncology, hematology or hematology/oncology.
- Experience in the pharmaceutical/biotechnology industry; clinical academic medicine or clinical medical practice settings in the field of hematology and/or oncology
- Oncology clinical drug development process experience in the conduct/participation of clinical trials (investigator initiated, company sponsored or cooperative group trials) and their subsequent publications.
Preferred Qualifications include:
- Oncology clinical research and drug development experience focused on hematological malignancies, including multiple myeloma
- Robust knowledge of disease-specific research priorities, public health needs, competitor landscape, clinical practice trends and treatment guidelines evolution
- LI-GSK
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
