Rosie Ackerman-Johnson's Location
London, England, GB
Rosie Ackerman-Johnson's Work
- Head of Regulatory Affairs and Quality @ Theolytics
- Senior Regulatory Affairs Manager @ Theolytics
- Senior Manager, Regulatory Affairs @ Diamond Pharma Services
- Associate Manager and Clinical Trials Team Lead @ Diamond Pharma Services
- Regulatory Affairs Associate Manager @ Diamond Pharma Services
- Regulatory Affairs Senior Officer @ Diamond Pharma Services
- Regulatory Affairs Associate III @ Teva Pharmaceuticals
- Regulatory Affairs Officer @ Consilient Health
Rosie Ackerman-Johnson's Education
- The University of Sheffield
Bachelor's Degree (Biomedical Sciences, General)
2011 - 2014 - Aylesbury High School
High School
2003 - 2010
Rosie Ackerman-Johnson's Skills
- Leadership
- Rmp Creation
- Teamwork
- Variation Submission
- Microsoft Office
- Data Analysis
- Pharmaceutical Industry
- Regulatory Affairs
- Problem Solving
- Communication
Rosie Ackerman-Johnson's Summary
Rosie Ackerman-Johnson, based in London, England, GB, is currently a Head of Regulatory Affairs and Quality at Theolytics, bringing experience from previous roles at Theolytics and Diamond Pharma Services. Rosie Ackerman-Johnson holds a 2011 - 2014 Bachelor's Degree in Biomedical Sciences, General @ The University of Sheffield. With a robust skill set that includes Leadership, Rmp Creation, Teamwork, Variation Submission, Microsoft Office and more, Rosie Ackerman-Johnson contributes valuable insights to the industry.
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