Archiviertes Projekt - Program Leader Biotech
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Projektbeschreibung
You are an experienced Program Manager in the area of biotech/pharma and searching for an interesting project at a promising Biotech company in Germany? Then you might be the right person for the following position:
Program Leader:
* Operate as Interim Business Team Head and Program Leader in the clinical, regulatory and medical development as well as the lifecycle management
* Ownership for project tasks, and track progress to make certain deadlines are met
* Identifyandcommunicatecriticalprocessesorissueswithinproject(s) anddevelopsolutionstrategies
* Clinical development activities as needed in starting new clinical trials (all phases I-IV, local or global), conducting ongoing trials and analyzing the results from trials in close alignment with the clinical trial teams
* Regulatory activities for new or ongoing clinical trials including the generation of briefing books for health authorities, and organizing health authority meetings in close alignment with the regulatory teams
* Develop and implement project management tools
Your skill set:
* Experience in Program and/or Project Management in biological and/or drug development and in the management of cross functional (development) teams
* Good understanding of drug development requirements and activities involving Nonclinical, Clinical, CMC, Regulatory Affairs, and Commercial aspects
Parameter:
Volume: 40 h/Week
Start: Jan. 2021
Duration: 6 month +
Looking forward to get your application!
Best regards,
Program Leader:
* Operate as Interim Business Team Head and Program Leader in the clinical, regulatory and medical development as well as the lifecycle management
* Ownership for project tasks, and track progress to make certain deadlines are met
* Identifyandcommunicatecriticalprocessesorissueswithinproject(s) anddevelopsolutionstrategies
* Clinical development activities as needed in starting new clinical trials (all phases I-IV, local or global), conducting ongoing trials and analyzing the results from trials in close alignment with the clinical trial teams
* Regulatory activities for new or ongoing clinical trials including the generation of briefing books for health authorities, and organizing health authority meetings in close alignment with the regulatory teams
* Develop and implement project management tools
Your skill set:
* Experience in Program and/or Project Management in biological and/or drug development and in the management of cross functional (development) teams
* Good understanding of drug development requirements and activities involving Nonclinical, Clinical, CMC, Regulatory Affairs, and Commercial aspects
Parameter:
Volume: 40 h/Week
Start: Jan. 2021
Duration: 6 month +
Looking forward to get your application!
Best regards,
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