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Novartis
Clinical Program Leader
Job Description
Serves as International Clinical Project Leader, Regional Therapeutic area representative to International Clinical Teams, or Medical Advisor to teams. Contributes to continuous improvement process. Designs Proof of Concept trials. Provides input to Clinical Protocol Summaries and Clinical Trial Protocols. Makes decisions regarding monitoring safety, eligibility, enrollment and data consistency. Provides medical expertise and medical evaluation of questions regarding patient care Provides Medical Expertise in support of other Novartis departments. Provides medical and scientific clinical research expertise in the development of overall strategy and objectives of the Early Clinical Development Plan. Writes and reviews abstracts/manuscripts, etc. for presentation/publications at internal/external meetings. Preparation and implementation of project specific training programs and training materials for internal and external staff. Participates in multidisciplinary task forces in support of continuous improvement and other management objectives. Represents company as medical expert to local medical community and to Health Authorities in support of projects. Establish/foster contacts to the clinical/scientific community and external experts.
Minimum requirements
MD Required. Need 3-5 pharma/biotech industry experience in drug development - clinical trials. Must have Phase I Oncology proof-of-concept clinical trial designs expertise. Knowledge of PK/PD and basic statistics. Proven ability to analyze and interpret efficacy and safety data relating to assigned area Medical/scientific writing skills. Knowledge of GCP and world wide regulatory requirements relating to assigned area. Effective written and oral communication skills.
Apply:
For faster processing, please apply online and directly to the employer. Specific instructions on how to apply are available. (recommended)
Clinical Program Leader
Job Description
Serves as International Clinical Project Leader, Regional Therapeutic area representative to International Clinical Teams, or Medical Advisor to teams. Contributes to continuous improvement process. Designs Proof of Concept trials. Provides input to Clinical Protocol Summaries and Clinical Trial Protocols. Makes decisions regarding monitoring safety, eligibility, enrollment and data consistency. Provides medical expertise and medical evaluation of questions regarding patient care Provides Medical Expertise in support of other Novartis departments. Provides medical and scientific clinical research expertise in the development of overall strategy and objectives of the Early Clinical Development Plan. Writes and reviews abstracts/manuscripts, etc. for presentation/publications at internal/external meetings. Preparation and implementation of project specific training programs and training materials for internal and external staff. Participates in multidisciplinary task forces in support of continuous improvement and other management objectives. Represents company as medical expert to local medical community and to Health Authorities in support of projects. Establish/foster contacts to the clinical/scientific community and external experts.
Minimum requirements
MD Required. Need 3-5 pharma/biotech industry experience in drug development - clinical trials. Must have Phase I Oncology proof-of-concept clinical trial designs expertise. Knowledge of PK/PD and basic statistics. Proven ability to analyze and interpret efficacy and safety data relating to assigned area Medical/scientific writing skills. Knowledge of GCP and world wide regulatory requirements relating to assigned area. Effective written and oral communication skills.
Apply:
For faster processing, please apply online and directly to the employer. Specific instructions on how to apply are available. (recommended)
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