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Clinical Scientific Associate Director, Contract, Switzerland
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Design, Client
Projektbeschreibung
CLINICAL SCIENTIFIC ASSOCIATE DIRECTOR, CONTRACT, SWITZERLAND
We have an exclusive contract role available to work onsite with a renowned global pharmaceutical company in Basel, Switzerland. This particular global pharmaceutical company is looking for Clinical Scientific Associate Director with thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process.
As a Clinical Scientific Associate Director (CSAD) you will be responsible primarily for Study level clinical activities but also for limited program level activities including supporting the GPMD in developing the scientific and operational strategy of assigned clinical trials to support the overall clinical development plan. This includes but is not limited to protocol development and implementation data collection, analysis, review, reporting and publishing in compliance with Our Client processes, adherence to quality standards and GCP/ICH and regulatory guidance.
The ideal candidate should have 3-5 years technical and operational experience in planning, executing, reporting and publishing clinical studies in industry or Academia with Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. Master's or PharmD. PhD or MD strongly preferred and demonstrates excellent scientific writing skills. English is the only language requirement for the role; the position offers a competitive salary.
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
Please note there is a job description available on request.
We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.
Kind regards,
Neha Sharma
Michael Bailey Associates
Job code: 108631
Key words: clinical trials, project management, Clinical Development Plan (CDP), Quality, SOPs, ICH, Good Clinical Practice, clinical trial design, statistics, regulatory processes, clinical development process, Pharmaceutical, CRFs, protocol deviations, questionnaires, diaries, translations, edit checks, Data Monitoring, Adjudication statistical analysis methodology Protocols, SMT, GCT, GPT, Reporting and Analysis Planning (RAP), planning, monitoring, clinical trial data, clinical study, drug development, Switzerland, Basel
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
We have an exclusive contract role available to work onsite with a renowned global pharmaceutical company in Basel, Switzerland. This particular global pharmaceutical company is looking for Clinical Scientific Associate Director with thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and clinical development process.
As a Clinical Scientific Associate Director (CSAD) you will be responsible primarily for Study level clinical activities but also for limited program level activities including supporting the GPMD in developing the scientific and operational strategy of assigned clinical trials to support the overall clinical development plan. This includes but is not limited to protocol development and implementation data collection, analysis, review, reporting and publishing in compliance with Our Client processes, adherence to quality standards and GCP/ICH and regulatory guidance.
The ideal candidate should have 3-5 years technical and operational experience in planning, executing, reporting and publishing clinical studies in industry or Academia with Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. Master's or PharmD. PhD or MD strongly preferred and demonstrates excellent scientific writing skills. English is the only language requirement for the role; the position offers a competitive salary.
We welcome applications of consultants' who match most of the above requirements and are available on a short notice. There is a competitive Hourly rate available for the contract; alternative market rates are also welcome.
Please note there is a job description available on request.
We hope the role will be of interest to you and understand that further information may be required before making an application to the end client, please feel free to send either your full name, contact details or a complete CV via this website and I will endeavour to get back to you with further information on the role and answer any questions you may have.
Kind regards,
Neha Sharma
Michael Bailey Associates
Job code: 108631
Key words: clinical trials, project management, Clinical Development Plan (CDP), Quality, SOPs, ICH, Good Clinical Practice, clinical trial design, statistics, regulatory processes, clinical development process, Pharmaceutical, CRFs, protocol deviations, questionnaires, diaries, translations, edit checks, Data Monitoring, Adjudication statistical analysis methodology Protocols, SMT, GCT, GPT, Reporting and Analysis Planning (RAP), planning, monitoring, clinical trial data, clinical study, drug development, Switzerland, Basel
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Medien/Design