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Regulatory Specialist
4 weeks ago
SRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the primary interface between global functions and affiliates to deliver clinical development regulatory strategies, operations and outcomes. Key Responsibilities:
- Manage a portfolio of CTAs including preparation and distribution of documentation associated with new initial CTAs and all CTA maintenance activities such as substantial amendments, end of trial notifications etc.
- Provide advice on submission strategy, country requirements, etc. as well as operational support for Regulatory submission preparation and processing of amendments.
- Review of and input on documents related to clinical trial submissions managed by other stakeholders.
- Ensure approved company CTA processes are followed within agreed timelines.
- Review and maintain awareness of regulatory intelligence relating to clinical trials and advise stakeholders accordingly.
- Ensure all relevant databases and activity trackers are populated within agreed timelines.
- Provide technical support on document preparation.
- Undertake all necessary training in order to achieve compliance with internal/external processes.
- Provide operational support for the Clinical Trial Strategy & Submissions Team as required.
- Comply with the company's policies and procedures.
- At least 2-years CTA experience in global clinical trial submissions to regulatory agencies.
- Experience working effectively across cultures and in a complex matrix environment.
- Good Information Technology skills, proven ability to utilise a variety of computer application packages.
- Proactive verbal and written communication style at all levels.
- Has excellent communication/presentation skills, written and verbal; fluency in English.
- Strong proven personal development and motivational skills.
- Strong interpersonal, organisational and team working skills.
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Regulatory Specialist
2 months ago
Maidenhead, Berkshire, United Kingdom SRG Full timeSRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...
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Regulatory Specialist
4 weeks ago
Maidenhead, Berkshire, United Kingdom SRG Full timeSRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote. The Role: The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the...
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Regulatory Specialist
4 weeks ago
Maidenhead, United Kingdom SRG Full timeSRG are currently looking for Regulatory Specialist for a Global Pharmaceutical Company who have opened new vacancies within their Regulatory team on an initial 12 Month basis to be based at their office in Maidenhead/Remote.The Role:The Regulatory Associate is responsible for providing global regulatory expertise for Clinical Trials. They are the primary...
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Regulatory Consultant
4 weeks ago
Maidenhead, United Kingdom Proclinical Full timeProclinical are recruiting a Regulatory Consultant for a biotech organisation. This role is on a contract basis with the ability to work remotely from anywhere in the UK. **Responsibilities**: - Guide the regulatory evaluation of commercial/medical resources working in collaboration with commercial and medical teams and external regulatory associates. -...
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Globla Regulatory Strategist
2 weeks ago
Maidenhead, United Kingdom ProClinical Full time**Salary**: Highly Competitive Salary Job type: ContractDiscipline: Consultant / Specialist, Officer /Associate, RA Intelligence**Location**: United Kingdom- Maidenhead, England - Posting date: 23 Apr 2024 Reference: RA.PD.60052 **Global Regulatory Strategist**: - Remote - Contract** Proclinical is seeking a Global Regulatory Strategist who will play a...
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Regulatory Affairs Product Specialist
1 week ago
Slough, Berkshire, United Kingdom Smiths Interconnect Full timeSmiths Interconnect is a leading provider of technically differentiated electronic components, subsystems, microwave and radio frequency products that connect , protect and control critical applications in the commercial aviation, defence, space, medical, rail, semi conductor test and industrial markets. Employing over 2,000 people globally our in house...
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Regulatory Affairs Manager
2 weeks ago
Maidenhead, Windsor and Maidenhead, United Kingdom AbbVie Full timeJob DescriptionRegulatory Affairs ManagerJoin us at Abbvie, in our Maidenhead office as a Regulatory Affairs Manager. We offer a hybrid working model, excellent career progression opportunities, and a comprehensive benefits package. This is an opportunity to be part of our UK regulatory leadership team and make a significant impact on our business.About the...
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Specialist assessor
4 weeks ago
Maidenhead, Berkshire, United Kingdom Windsor Forest Colleges Full timeWindsor Forest College Group is looking for SpecialistAssessortojoin the BCA /Langley team on a full-time basis. Find out more about this role by reading the information below, then apply to be considered. Specialist Assessor We are looking for someone To be responsible for the provision of assessment, support, and guidance for learners with Learning...
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Maidenhead, United Kingdom Hays Specialist Recruitment Limited Full timeRegulatory Affairs Senior Manager, EU, contract job, strategy Regulatory Affairs Senior Manager - EU **Your new company **This well known biotech company is looking for an experienced Senior Manager in Regulatory Affairs to join their EU, Canada and Partner markets team, this is a 12 month contract job with scope for extension. You will be responsible for EU...
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Maidenhead, Windsor and Maidenhead, United Kingdom Hays Specialist Recruitment Limited Full timeRegulatory Affairs Senior Manager, EU, contract job, strategyRegulatory Affairs Senior Manager - EU**Your new company**This well known biotech company is looking for an experienced Senior Manager in Regulatory Affairs to join their EU, Canada and Partner markets team, this is a 12 month contract job with scope for extension. You will be responsible for EU...
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Regulatory Affairs Manager
4 weeks ago
Maidenhead, United Kingdom AbbVie Full timeJob DescriptionRegulatory Affairs ManagerJoin us at Abbvie, in our Maidenhead office as a Regulatory Affairs Manager. We offer a hybrid working model, excellent career progression opportunities, and a comprehensive benefits package. This is an opportunity to be part of our UK regulatory leadership team and make a significant impact on our business.About the...
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Slough, Berkshire, United Kingdom Smiths Interconnect Full timeJob Description About us: Smiths Interconnect is a leading provider of technically differentiated electronic components, subsystems, microwave and radio frequency products that connect , protect and control critical applications in the commercial aviation, defence, space, medical, rail, semi conductor test and industrial markets. Employing over 2,000...
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Director of Regulatory Affairs
1 month ago
Slough, Berkshire, United Kingdom Verbatim Pharma Full timeRegulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the...
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Director of Regulatory Affairs
1 month ago
Slough, Berkshire, United Kingdom Verbatim Pharma Full timeRegulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the...
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Director of Regulatory Affairs
4 weeks ago
Slough, Berkshire, United Kingdom Verbatim Pharma Full timeRegulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the...
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Director of Regulatory Affairs
4 weeks ago
Slough, Berkshire, United Kingdom Verbatim Pharma Full timeRegulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives of some of the...
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Director of Regulatory Affairs
2 weeks ago
Slough, Berkshire, United Kingdom Verbatim Pharma Full timeJob Description Regulatory Affairs - Clinical Trial Services - Hybrid Opportunity Are you ready to advance your career with a leader in Clinical Services? Providing the opportunity to specialise in a niche area of a business who have 3 key divisions, providing exposure to an area of the pharmaceutical industry being directly involved in saving the lives...
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Clinical Trial Specialist
1 month ago
Maidenhead, Berkshire, United Kingdom Consult Full timeMaidenhead Very competitive salary Hybrid working 2x a week Initial 12 month contract which is likely to be extended This is an excellent opportunity for an experienced CTS Coordinator to join a global pharmaceutical company for an initial 12 months, with the potential for this to be extended. This role has come about due to expansion and an increase in...
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Clinical Trial Specialist
1 month ago
Maidenhead, Berkshire, United Kingdom Consult Full timeMaidenhead Very competitive salary Hybrid working 2x a week Initial 12 month contract which is likely to be extended This is an excellent opportunity for an experienced CTS Coordinator to join a global pharmaceutical company for an initial 12 months, with the potential for this to be extended. This role has come about due to expansion and an increase in...
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Clinical Trial Specialist
4 weeks ago
Maidenhead, Berkshire, United Kingdom Consult Full timeMaidenhead Very competitive salary Hybrid working 2x a week Initial 12 month contract which is likely to be extended This is an excellent opportunity for an experienced CTS Coordinator to join a global pharmaceutical company for an initial 12 months, with the potential for this to be extended. This role has come about due to expansion and an increase in...