- Merck & Co. (North Wales, PA)
- …health. - Responsibilities : This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Merck & Co. (Upper Gwynedd, PA)
- …and accountable for the end-to-end lifecycle management for our company's late - stage multi-tumor assets. This includes the breadth/depth of development ... launches. The Vice President (VP) will work collaboratively with Oncology VP TA heads directly as well as through...of Asset Team Leads who will develop individual molecule late - stage development plans; will work across TA… more
- Merck & Co. (North Wales, PA)
- …human health.This position supports statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (North Wales, PA)
- …mechanistic PK-PD models and QSP models for decision making in early and/or late - stage clinical development Experience with mechanistic modeling for antibody ... to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-PCC to registration. Directors are leaders in the field… more
- Pfizer (Collegeville, PA)
- …development strategy for programs within the Late - Stage Oncology portfolio. **Key Responsibilities** + Clinical development professional maintaining ... RAVE, SpotFire, SOCs-PRO or other similar platform **Preferred Qualifications** + Industry/CRO Clinical Research experience in Oncology + Oncology Fellowship… more
- Pfizer (Collegeville, PA)
- … trial(s) in support of the development strategy for programs within the Late - Stage Oncology portfolio. **Position Responsibilities** + Maintains current ... scientific and clinical knowledge in the specific therapeutic and disease area(s)... Research experience in the Phase 3/pivotal space in Oncology , ideally on the side of the sponsor. +… more
- Merck (North Wales, PA)
- …health. **Responsibilities** **:** This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
- Sumitomo Pharma (Philadelphia, PA)
- …products in the US, Canada, and Europe, and a diverse pipeline of early- to late - stage assets, we aim to accelerate discovery, research, and development to bring ... + Represent the Company at national, regional, and local oncology meetings and conferences. + Maintain clinical ...Canada, and Europe, a diverse pipeline of early- to late - stage assets, and in-house advanced technology capabilities,… more
- Merck (Upper Gwynedd, PA)
- …and accountable for the end-to-end lifecycle management for our company's late - stage multi-tumor assets. This includes the breadth/depth of development ... launches. The Vice President (VP) will work collaboratively with Oncology VP TA heads directly as well as through...of Asset Team Leads who will develop individual molecule late - stage development plans; will work across TA… more
- Merck (North Wales, PA)
- …mechanistic PK-PD models and QSP models for decision making in early and/or late - stage clinical development + Experience with mechanistic modeling for ... to clinical pharmacology, mechanistic PK-PD modeling and pharmacometrics of oncology drugs from post-PCC to registration. Directors are leaders in the field… more
- Merck (North Wales, PA)
- …health. This position supports statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. Accountability ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.… more
