Aktuelle Jobs im Zusammenhang mit Medical Director/sr Medical Director Early Clinical - Morges - Incyte Corporation
-
Morges, Waadt, Schweiz Incyte VollzeitOverviewSummaryThis position is responsible for implementing early clinical development efforts for Incyte's Dermatology, Immunology, Rheumatology products (preclinical candidate nomination through transition to registrational studies)Duties and ResponsibilitiesLeads development efforts for assets post-candidate selection through first in human trials,...
-
Senior Medical Director, Early Clinical Development
vor 2 Wochen
Morges, Waadt, Schweiz Incyte VollzeitOverviewSummaryThe Sr. Director Clinical Research Scientist is responsible for working with the physicians within Clinical to provide clinical research support for programs as assigned by phase or therapeutic area.Duties and ResponsibilitiesAct within compliance and legal requirements as well as within company guidelines.Contribute positively to a strong...
-
Associate Director, Principal Medical Writing II
vor 2 Wochen
Morges, Schweiz Incyte Corporation VollzeitOverview The Associate Director, Principal Medical Writer II is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross‑functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators’ Brochures [IBs], Clinical Study Reports...
-
Associate Director, Principal Medical Writing II
Vor 3 Tagen
Morges, Schweiz Incyte Corporation VollzeitOverview The Associate Director, Principal Medical Writer II is responsible for the development of clinical documents for submissions to regulatory authorities globally. Provides strategic direction to cross‑functional project teams with minimal oversight to ensure that clinical documents (eg, Investigators’ Brochures (IBs), Clinical Study Reports...
-
Director, Clinical Research Scientist
vor 2 Wochen
Morges, Schweiz Incyte Corporation VollzeitOverview: **Summary** This position is responsible for working with the physicians and other clinical scientists within Early Clinical Development to provide clinical research support for early phase clinical programs in patients as assigned by therapeutic area and type of therapy. Primary focus will be on hematology & oncology programs.
-
Director, Clinical Research Scientist
Vor 7 Tagen
Morges, Schweiz Incyte Corporation VollzeitIncyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and...
-
Director, Clinical Collaborations Eimea
Vor 3 Tagen
Morges, Schweiz Accuray VollzeitGive hope. Give health. Make your mark in the fight against cancer. At Accuray, we make a direct and powerful impact on the lives of cancer patients every day — helping them live longer, better lives. But our commitment to innovation offers a truly unique opportunity: the chance to change the fight against cancer — helping to develop, introduce and...
-
(Sr) Director Health Economics
Vor 7 Tagen
Morges, Schweiz Incyte Corporation Vollzeit**Summary** The main objective of this position is to develop appropriate health economic and outcomes research evidence to characterize INCYTE products value at launch and throughout their life cycle. **Responsibilities** - Initial focus will be on the upcoming launches including pemigatinib and tafasitamab but also earlier products in the pipeline. -...
-
Manager - Sr Manager Clinical QA
vor 2 Wochen
Morges, Schweiz Incyte Corporation VollzeitSummary The Sr GCP Auditor is responsible for providing primarily ex-US Pharmacovigilance (PVG) audit support for QA management and oversight of global PVG activities of Clinical Development teams to the Head of Incyte QA-GCP. Secondarily the Sr Auditor is responsible for GCP support for clinical development. This job will include the execution and...
-
Associate Director Diagnostic Biomarker Europe
vor 1 Woche
Morges, Schweiz Incyte Corporation Vollzeit**Job Summary (Primary function)** The Associate Director Diagnostic Biomarker, Europe is responsible for the coordination and the local implementation of the biomarker testing strategy in Europe for Targeted Therapies with focus on a Rare Disease Brand. The Associate Director enables appropriate testing in order to identify patients with unmet needs who...
Medical Director/sr Medical Director Early Clinical
vor 2 Wochen
**Summary**
This position is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though POC) for oncology.
**Duties and Responsibilities**:
- Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilence and clinical operations
- Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, investigator brochure, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans
- Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies
- Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development
- Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development
- Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders
- Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies
- Works in partnership with medical affairs for successful launch of future anti¬neoplastic agents
- Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents
- Provides guidance for successful implementation and accomplishment of investigator initiated trials related to product development and life cycle management of a compound
- Contribute positively to a strong culture of business integrity and ethics
- Act within compliance and legal requirements as well as within company guidelines
**Requirements**:
- M.D. or D.O. degree with a minimum of 3 - 5 years of experience (6+ years - senior) in oncology drug development in a biotechnology or pharmaceutical company, clinical research experience in academia also acceptable
- Board certified or eligible in Oncology preferred
- Experience with early phase oncology trials
- Excellent written and oral communication skills
- Ability to multi-task and work in a face paced environment
**Summary**
This position is responsible for implementing clinical drug efforts for Incyte's oncology products (Phase I though POC) for oncology.
**Duties and Responsibilities**
- Provides medical and scientific expertise for internal cross-functional team members for development of specific anti-neoplastic agents including discovery scientists, medical scientists, biostatisticians, pharmacokineticists, pharmacovigilence and clinical operations
- Facilitates the development of key internal and external documents pertaining to product development including clinical study protocol, investigator brochure, informed consents, CRFs, CSRs, meeting abstracts, scientific journal publications, strategy documents and project plans
- Collaborates with external vendors such as CROs, external imaging and laboratory resources, as well as global pharmaceutical companies for successful implementation and conduct of early phase and registration global clinical studies
- Serves as a source for medical and scientific expertise in oncology for outlining design strategy and execution for anti-cancer drug development
- Liaises with discovery science to facilitate and further the development of investigational agents from a preclinical stage to clinical development
- Represents Incyte Corporation at key national and international medical and scientific meetings including participation in advisory boards with key opinion leaders
- Detects and analyzes emergent issues during clinical drug development and develops and implements mitigating strategies
- Works in partnership with medical affairs for successful launch of future anti¬neoplastic agents
- Implements the highest ethical and regulatory standards during the investigation and development of anticancer agents
- Provides guidance for successful implementation and accomplishment of investigator initiated trials related to product development and life cycle management of a compound
- Contribute positively to a strong culture of business integrity and ethics
- Act within compliance and legal requirements as well as within company guidelines
- **Requirements**
- M.D. or D.O. degree with a minimum of 3 - 5 years of experience (6+ years - senior) in oncology drug development in a biotechnology or pharmaceutical company, clinical research experience in academia also acceptable
- Board certified or eligible in Oncology preferred
- Experience with early phase oncology trials
- Ex
