Head of Medical Writing
5 days ago
Head of Medical Writing and Regulatory Affairs
The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team.
They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources.
This is a hybrid role in Central London. Applicants must be prepared to go on site 4 days per week.
Responsibilities:
- Take full accountability of all medical writing and regulatory activities.
- Direct line management responsibilities for the Medical Writing team. You will be managing two employees
- Provide regulatory expertise to project teams on all aspects of the clinical trials process.
- Support the organisation and preparation of regulatory submissions, ensuring accuracy and regulatory appropriateness.
- Oversee the preparation, and submission, of all clinical study documentation in accordance with regulatory requirements.
- Establish and maintain excellent sponsor relationships.
Required experience:
- 5-10 years of experience authoring pharmaceutical regulatory documentation, across phases I-III
- Line management experience desired
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Head of Medical Writing
2 weeks ago
London, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a...
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Head of Medical Writing
2 weeks ago
London, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This...
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Head of Medical Writing
2 weeks ago
London,, UK, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This...
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Head of Medical Writing
2 weeks ago
London, United Kingdom Warman O'Brien Full timeJob Description Head of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and...
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Head of Medical Writing
5 days ago
London Area, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory Affairs The Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This...
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Head of Medical Writing
2 weeks ago
London Area, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a...
-
Head of Medical Writing
2 weeks ago
London Area, United Kingdom Warman O'Brien Full timeHead of Medical Writing and Regulatory AffairsThe Head of Medical Writing and Regulatory Affairs provides a senior level of expertise and management for our client's medical writing team. They will be responsible for the fulfilment of medical writing and regulatory activities, ensuring optimal allocation of medical writing and regulatory resources. This is a...
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London, United Kingdom Arevna Full time €70,000A leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation. HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON). MUST BE ABLE TO WORK IN THE UK...
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London, United Kingdom Arevna Full timeA leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...
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London,, UK, United Kingdom Arevna Full timeA leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...
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London Area, United Kingdom Arevna Full timeA leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation. HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON). MUST BE ABLE TO WORK IN THE UK...
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Head of Medical Writing
1 month ago
London Area, United Kingdom Arevna Full timeA leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...
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Head of Medical Writing
1 month ago
London Area, United Kingdom Arevna Full timeA leading Contract Research Organisation (CRO) specializing in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.HYBRID - £70K+ - MUST BE SITE BASED 4 DAYS (CENTRAL LONDON).MUST BE ABLE TO WORK IN THE UK WITHOUT...
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London, United Kingdom Barrington James Full timeA prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions . This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...
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London Area, United Kingdom Barrington James Full timeA prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients, is seeking a talented and experienced Head of Medical Writing and Regulatory Submissions . This role offers the opportunity to lead and manage teams within a dynamic, research-driven environment, dedicated to advancing...