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Regulatory Affairs Specialist - Clinical Trials
Eingestellt von Darwin Recruitment
Gesuchte Skills: Support
Projektbeschreibung
Regulatory Affairs Specialist - Clinical Trials
Darwin Recruitment AG are partnered with a global leader in the Pharma industry, who are looking for a Senior Regulatory Affairs Specialist. In this position you will work closely with professionals in Switzerland a provide regulatory support of eSubmissions for Clinical Trials
Your tasks:
- Developing Regulatory Affairs strategies and managing departmental projects
- Preparing the country-specific RA registration files for Clinical Trials
- Facilitating the implementation of RA standards for new products
- Work in close cooperation with stakeholders around the globe
Your profile:
- Degree in a technical field or life sciences or equivalent formation
- Minimum three years of practical experience within the field of RA industry
- Ability to assess business risks and handle regulatory assignments
- Deep knowledge of Clinical Trials regulations and standards
- Excellent communication in English both verbal and written, any other language of advantage
- Entrepreneurial spirit and ability to think and act strategically
- Excellent communication skills
Please contact me with an updated CV if interested along with your earliest avaibility and rate expectations.
Darwin Recruitment AG are partnered with a global leader in the Pharma industry, who are looking for a Senior Regulatory Affairs Specialist. In this position you will work closely with professionals in Switzerland a provide regulatory support of eSubmissions for Clinical Trials
Your tasks:
- Developing Regulatory Affairs strategies and managing departmental projects
- Preparing the country-specific RA registration files for Clinical Trials
- Facilitating the implementation of RA standards for new products
- Work in close cooperation with stakeholders around the globe
Your profile:
- Degree in a technical field or life sciences or equivalent formation
- Minimum three years of practical experience within the field of RA industry
- Ability to assess business risks and handle regulatory assignments
- Deep knowledge of Clinical Trials regulations and standards
- Excellent communication in English both verbal and written, any other language of advantage
- Entrepreneurial spirit and ability to think and act strategically
- Excellent communication skills
Please contact me with an updated CV if interested along with your earliest avaibility and rate expectations.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges