Emma Witch
• Regulatory Submission Strategy - I lead global expert teams through the development of submission communication strategies (Storyboards), both... | Greater Liverpool Area, Greater Liverpool Area, United Kingdom
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Emma Witch’s Emails em****@as****.com
Emma Witch’s Phone Numbers No phone number available.
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Emma Witch’s Location Greater Liverpool Area, Greater Liverpool Area, United Kingdom
Emma Witch’s Expertise • Regulatory Submission Strategy - I lead global expert teams through the development of submission communication strategies (Storyboards), both pre-data and post-data, that identify how the desired benefit-risk and labelling positions will be supported by clinical data • Regulatory Submission Document Delivery –I secure and lead teams of Medical Writers to deliver clinical-regulatory documents (Clinical Overview, Clinical Summary documents, Clinical Study Reports, Briefing Documents, Risk Management Plans, etc) according to agreed Storyboards, and to time, cost and quality • Facilitating Expert Decision-Making – I ensure that decisions (during both the planning and delivery stages of a Regulatory Submission) are made by the right people, at the right time, with the right information, through effective facilitation and project management skills I work from home, and I am used to travelling extensively, and working across different time zones.
Emma Witch’s Current Industry Regulatory Medical Writer
Emma
Witch’s Prior Industry
Astrazeneca
|
Regulatory Medical Writer
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Work Experience
Regulatory Medical Writer
Freelance
Sat Jul 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Astrazeneca
Principal Regulatory Medical Writer
Thu Jan 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Astrazeneca
Key Achievements-Regulatory Submission Strategy
Thu Jan 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Astrazeneca
Key Achievements: Regulatory Submission Document Delivery
Thu Jan 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)
Astrazeneca
Key Achievements- Facilitating Expert Decision-Making
Thu Jan 01 1998 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Jan 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Emma Witch Email Addresses
FAQ About Emma Witch
-
Emma Witch is located at
Greater Liverpool Area, Greater Liverpool Area, United Kingdom -
Emma Witch is a
• Regulatory Submission Strategy - I lead global expert teams through the development of submission communication strategies (Storyboards), both pre-data and post-data, that identify how the desired benefit-risk and labelling positions will be supported by clinical data • Regulatory Submission Document Delivery –I secure and lead teams of Medical Writers to deliver clinical-regulatory documents (Clinical Overview, Clinical Summary documents, Clinical Study Reports, Briefing Documents, Risk Management Plans, etc) according to agreed Storyboards, and to time, cost and quality • Facilitating Expert Decision-Making – I ensure that decisions (during both the planning and delivery stages of a Regulatory Submission) are made by the right people, at the right time, with the right information, through effective facilitation and project management skills I work from home, and I am used to travelling extensively, and working across different time zones. Regulatory Medical Writer -
Emma Witch currently works in the
Regulatory Medical Writer -
Emma Witch specializes in
• Regulatory Submission Strategy - I lead global expert teams through the development of submission communication strategies (Storyboards), both pre-data and post-data, that identify how the desired benefit-risk and labelling positions will be supported by clinical data • Regulatory Submission Document Delivery –I secure and lead teams of Medical Writers to deliver clinical-regulatory documents (Clinical Overview, Clinical Summary documents, Clinical Study Reports, Briefing Documents, Risk Management Plans, etc) according to agreed Storyboards, and to time, cost and quality • Facilitating Expert Decision-Making – I ensure that decisions (during both the planning and delivery stages of a Regulatory Submission) are made by the right people, at the right time, with the right information, through effective facilitation and project management skills I work from home, and I am used to travelling extensively, and working across different time zones. -
Emma Witch speaks the following languages:
No languages available. -
Emma Witch has prior experience in the following industries:
Astrazeneca , Astrazeneca , Astrazeneca , Astrazeneca -
Emma Witch has the following professional experience:
Regulatory Medical Writer , Astrazeneca , Astrazeneca , Astrazeneca , Astrazeneca . -
You can view Emma Witch’s
LinkedIn profile at LinkedIn URL. -
Emma Witch’s work email addresses are
[email protected] . -
Emma Witch works at
Regulatory Medical Writer
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