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Clinical Research Operations Manager, Contract, Switzerland
Eingestellt von Michael Bailey Associates - UK Contracts
Gesuchte Skills: Marketing, Client
Projektbeschreibung
Clinical Research Operations Manager, CONTRACT, Pharmaceutical, Switzerland
PROCESS MAPPING OF R&D PHARMACEUTICAL ENVIRONMENT
A global pharmaceutical company has an opportunity for an executive to implement important process mapping systems throughout their R&D environment. This role has cross-functional responsibilities across all departments including Clinical Research, PV, RA, Manufacturing and Development with the objective of ensure numerous change management objectives. This position works as the coordinator of departmental Heads and in the management of Project Managers.
REQUIREMENTS
- Experience in working with Pre-Marketing Submission Dossiers is an essential skill set
- Should have worked as a Regulatory Affairs specialist/Manager for a CRO for 3 to 5 years with extensive Clinical Trial Application experience
- Must have leadership skills and had Project execution experience
- Experience within Clinical Research/Clinical Trials, in particular Clinical Dossier management is important (Pre-Marketing dossier compilation and submission)
-More than 2 years of direct experience in Change/Programme Management, must have a track record in implementing and meeting numerous milestone/change management objectives.
- In-depth knowledge of the life science sector, more than 3 years of direct experience in the life science sector is essential. Must understand how the pharmaceutical industry works and the importance of each department.
- You are somebody who can become a "Subject Matter Expert" in a given field with ease and in a timely manner.
- Excellent Communication skills
- English is the only language requirement
I hope that 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 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.
Best regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 106844
KEYWORDS: Clinical Trial Application, CTA "Process Mapping", PV, RA, "regulatory Affairs", Manufacturing, "clinical research", operations, "Change Management", "Transformational Management", "Project Management", Operations Management, "Subject Matter", Pharmaceutical, IT/IS, Life sciences, DRA operations. Clinical research operations,Pre-marketing dossiers, clinical trials, Switzerland, Basel
Michael Bailey International is acting as an Employment Business in relation to this vacancy.
PROCESS MAPPING OF R&D PHARMACEUTICAL ENVIRONMENT
A global pharmaceutical company has an opportunity for an executive to implement important process mapping systems throughout their R&D environment. This role has cross-functional responsibilities across all departments including Clinical Research, PV, RA, Manufacturing and Development with the objective of ensure numerous change management objectives. This position works as the coordinator of departmental Heads and in the management of Project Managers.
REQUIREMENTS
- Experience in working with Pre-Marketing Submission Dossiers is an essential skill set
- Should have worked as a Regulatory Affairs specialist/Manager for a CRO for 3 to 5 years with extensive Clinical Trial Application experience
- Must have leadership skills and had Project execution experience
- Experience within Clinical Research/Clinical Trials, in particular Clinical Dossier management is important (Pre-Marketing dossier compilation and submission)
-More than 2 years of direct experience in Change/Programme Management, must have a track record in implementing and meeting numerous milestone/change management objectives.
- In-depth knowledge of the life science sector, more than 3 years of direct experience in the life science sector is essential. Must understand how the pharmaceutical industry works and the importance of each department.
- You are somebody who can become a "Subject Matter Expert" in a given field with ease and in a timely manner.
- Excellent Communication skills
- English is the only language requirement
I hope that 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 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.
Best regards,
Neha Sharma
MBA Michael Bailey Associates
Job Code: 106844
KEYWORDS: Clinical Trial Application, CTA "Process Mapping", PV, RA, "regulatory Affairs", Manufacturing, "clinical research", operations, "Change Management", "Transformational Management", "Project Management", Operations Management, "Subject Matter", Pharmaceutical, IT/IS, Life sciences, DRA operations. Clinical research operations,Pre-marketing dossiers, clinical trials, 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, Marketing/Vertrieb