Healthcare Jobs in United Kingdom

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Associate Director Regulatory Affairs at Aero Healthcare United Kingdom
london, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
MSK Physiotherapist at Vivid Healthcare Search Limited
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Health Care Assistant at Harley Street Healthcare Clinic
London, Alberta, United Kingdom - Full Time
Skills Needed
N/A
"Healthcare Assistant" or "Health Care Assistant" or "HCA" OR "Support Worker" O at NEW BEGINNINGS HEALTHCARE SERVICES LTD
London, Alberta, United Kingdom - Full Time
Skills Needed
N/A
https://applywave.app/visa-sponsorship-jobs/healthcare-assistant-riverside-surge at Riverside Surgery
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
https://careers.diaverum.com/job/Ipswich-Healthcare-Assistant-Ipswich-IP4-5PD/13 at Indeed
Middlesex, Middlesex - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Clinical Administrator at East Sussex Healthcare NHS Trust
Manchester, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 22 year(s)
Administration Coordinator at Jamie Pugh Dental Healthcare Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Talent Acqusition Specialist at Michael Little Healthcare Pty Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Warehouse / Logistics Operative at Simon Hegele Healthcare Solutions
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Physiotherapy Assistant at East Sussex Healthcare NHS Trust
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
MSK Physiotherapist at East Sussex Healthcare NHS Trust
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Payroll Specialist at Michael Little Healthcare Pty Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Clinical Study Specialist at REGENERON HEALTHCARE SOLUTIONS INC
England, East Suffolk - England, United Kingdom - Full Time
Skills Needed
N/A
Senior care worker at SPRINGWOOD HEALTHCARE SERVICES LTD
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Risk & Compliance Investigator at Bestway Panacea Healthcare Limited
Manchester, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Associate Director Regulatory Affairs at Aero Healthcare United Kingdom
london, London - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

26 Jan, 27

Salary

120000.0

Posted On

28 Oct, 26

Experience

20 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

Why AstraZeneca?

At AstraZeneca, we follow the science and put patients first.

You will join a culture that values curiosity, courage and collaboration, where talented individuals are empowered to challenge convention and shape the future of healthcare. We invest in our people through meaningful career development, global mobility opportunities, leadership programmes and cutting-edge scientific innovation.

Our Oncology business continues to redefine what is possible in cancer treatment, creating opportunities for regulatory leaders to influence some of the most exciting programmes in the industry.

What you will do?

  • Lead cross functional teams in major regulatory submissions (MAA/CTR/IVDR/CTA), health authority interactions with EMA or national European health authorities, label discussions, and securing approvals. 
  • Develop and implement the program's regional or global strategy ensuring that it is crafted to deliver rapid approval with competitive labeling that is identified by the business, markets and patients. 
  • Craft the EU health authority engagement strategy and interaction plan, drive the formulation of the briefing document focused on strategy and scientific content, lead the team through meeting rehearsals and moderate the meeting itself. 
  • Key contribuiting members to the Global Regulatory Strategy Team (GRST) that includes regions, emerging markets, RA CMC, Labeling and members of the submission and execution team. Mentor and provide performance feedback to members of your GRST. 
  • Deliver regulatory milestones on your team including an assessment of risks and mitigations, emerging data, and the probability of success. Lead preparation of the regulatory strategy document and target product labeling in collaboration with the GRL. 
  • Own the negotiations with health authorities and initiate and deliver key regulatory documents. 
  • Plan and construct the global dossier and core prescribing information including product maintenance, supply and compliance activities. 
  • Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. 

Minimum Qualifications:

  • Bachelor's degree in Life Sciences, Pharmacy, Biomedical Sciences or a related scientific discipline with a
  • + 5 years’ experience in regulatory affairs, regulatory strategy, or drug development within the pharmaceutical or biotechnology industry; including preparation for major health authority interactions, development of briefing documents, contribution to labeling strategy, and support for regulatory submission planning and execution. Experience with filing of IVDR, CTR, CTAs, MAAs, lifecycle management activities, and regulatory pathways (relevant to oncology products is preferred)
  • Strong knowledge of global regulatory affairs across both early and late-stage development, with experience supporting or shaping regulatory strategies for major submissions and health authority, primarily In Europe. 
  • Outstanding communication, strategic thinking and problem-solving skills.
  • Experience operating effectively in a global matrix environment, lead through complexity, and drive alignment across multiple functions is essential. 

Preferred Qualifications:

  • Advanced degree preferred. 
  • Experience in Oncology is preferred. 
  • Prior experience with phase 3 design including end of phase 2 health authority interactions. 
  • Contribution to a regulatory approval including leading response team and labeling negotiations. 
  • Knowledge and understanding of guiding principles in drug development such as benefit/risk profile, dose selection or statistical design. 
  • Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. 
  • Ability to work strategically within a business critical and high-profile development program. 
  • Critical thinking on current global and regional regulatory science questions and good understanding of the corresponding scientific and clinical component. 

What success looks like

In this role, you will:

  • Deliver critical regulatory milestones for Oncology that support programme progression and approvals.
  • Build productive relationships with health authorities and key internal stakeholders.
  • Provide strategic leadership across complex, high-profile development programmes.
  • Influence decisions that drive patient access to innovative medicines in the EU market.

Inclusion & Diversity

AstraZeneca is an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome applications from all qualified candidates and make employment decisions without regard to legally protected characteristics.

Ready to make an impact?

Join AstraZeneca and help deliver the next generation of medicines that transform the lives of patients around the world.

Apply today to become part of a team where science, innovation and collaboration drive meaningful change.

Responsibilities

Why AstraZeneca?

At AstraZeneca, we follow the science and put patients first.

You will join a culture that values curiosity, courage and collaboration, where talented individuals are empowered to challenge convention and shape the future of healthcare. We invest in our people through meaningful career development, global mobility opportunities, leadership programmes and cutting-edge scientific innovation.

Our Oncology business continues to redefine what is possible in cancer treatment, creating opportunities for regulatory leaders to influence some of the most exciting programmes in the industry.

What you will do?

  • Lead cross functional teams in major regulatory submissions (MAA/CTR/IVDR/CTA), health authority interactions with EMA or national European health authorities, label discussions, and securing approvals. 
  • Develop and implement the program's regional or global strategy ensuring that it is crafted to deliver rapid approval with competitive labeling that is identified by the business, markets and patients. 
  • Craft the EU health authority engagement strategy and interaction plan, drive the formulation of the briefing document focused on strategy and scientific content, lead the team through meeting rehearsals and moderate the meeting itself. 
  • Key contribuiting members to the Global Regulatory Strategy Team (GRST) that includes regions, emerging markets, RA CMC, Labeling and members of the submission and execution team. Mentor and provide performance feedback to members of your GRST. 
  • Deliver regulatory milestones on your team including an assessment of risks and mitigations, emerging data, and the probability of success. Lead preparation of the regulatory strategy document and target product labeling in collaboration with the GRL. 
  • Own the negotiations with health authorities and initiate and deliver key regulatory documents. 
  • Plan and construct the global dossier and core prescribing information including product maintenance, supply and compliance activities. 
  • Partner with marketing companies (countries) and regional regulatory affairs staff to influence developing views/guidance. 

Minimum Qualifications:

  • Bachelor's degree in Life Sciences, Pharmacy, Biomedical Sciences or a related scientific discipline with a
  • + 5 years’ experience in regulatory affairs, regulatory strategy, or drug development within the pharmaceutical or biotechnology industry; including preparation for major health authority interactions, development of briefing documents, contribution to labeling strategy, and support for regulatory submission planning and execution. Experience with filing of IVDR, CTR, CTAs, MAAs, lifecycle management activities, and regulatory pathways (relevant to oncology products is preferred)
  • Strong knowledge of global regulatory affairs across both early and late-stage development, with experience supporting or shaping regulatory strategies for major submissions and health authority, primarily In Europe. 
  • Outstanding communication, strategic thinking and problem-solving skills.
  • Experience operating effectively in a global matrix environment, lead through complexity, and drive alignment across multiple functions is essential. 

Preferred Qualifications:

  • Advanced degree preferred. 
  • Experience in Oncology is preferred. 
  • Prior experience with phase 3 design including end of phase 2 health authority interactions. 
  • Contribution to a regulatory approval including leading response team and labeling negotiations. 
  • Knowledge and understanding of guiding principles in drug development such as benefit/risk profile, dose selection or statistical design. 
  • Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs. 
  • Ability to work strategically within a business critical and high-profile development program. 
  • Critical thinking on current global and regional regulatory science questions and good understanding of the corresponding scientific and clinical component. 

What success looks like

In this role, you will:

  • Deliver critical regulatory milestones for Oncology that support programme progression and approvals.
  • Build productive relationships with health authorities and key internal stakeholders.
  • Provide strategic leadership across complex, high-profile development programmes.
  • Influence decisions that drive patient access to innovative medicines in the EU market.

Inclusion & Diversity

AstraZeneca is an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome applications from all qualified candidates and make employment decisions without regard to legally protected characteristics.

Ready to make an impact?

Join AstraZeneca and help deliver the next generation of medicines that transform the lives of patients around the world.

Apply today to become part of a team where science, innovation and collaboration drive meaningful change.

Associate Director Regulatory Affairs at Aero Healthcare United Kingdom
london, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 20 year(s)
MSK Physiotherapist at Vivid Healthcare Search Limited
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Health Care Assistant at Harley Street Healthcare Clinic
London, Alberta, United Kingdom - Full Time
Skills Needed
N/A
"Healthcare Assistant" or "Health Care Assistant" or "HCA" OR "Support Worker" O at NEW BEGINNINGS HEALTHCARE SERVICES LTD
London, Alberta, United Kingdom - Full Time
Skills Needed
N/A
https://applywave.app/visa-sponsorship-jobs/healthcare-assistant-riverside-surge at Riverside Surgery
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
https://careers.diaverum.com/job/Ipswich-Healthcare-Assistant-Ipswich-IP4-5PD/13 at Indeed
Middlesex, Middlesex - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 3 year(s)
Clinical Administrator at East Sussex Healthcare NHS Trust
Manchester, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 22 year(s)
Administration Coordinator at Jamie Pugh Dental Healthcare Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Talent Acqusition Specialist at Michael Little Healthcare Pty Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Warehouse / Logistics Operative at Simon Hegele Healthcare Solutions
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Physiotherapy Assistant at East Sussex Healthcare NHS Trust
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
MSK Physiotherapist at East Sussex Healthcare NHS Trust
London, Leicestershire - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Payroll Specialist at Michael Little Healthcare Pty Ltd
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Clinical Study Specialist at REGENERON HEALTHCARE SOLUTIONS INC
England, East Suffolk - England, United Kingdom - Full Time
Skills Needed
N/A
Senior care worker at SPRINGWOOD HEALTHCARE SERVICES LTD
London, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 1 year(s)
Risk & Compliance Investigator at Bestway Panacea Healthcare Limited
Manchester, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 5 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
Registered Nurse at North of Superior Healthcare Group
England, London - England, United Kingdom - Full Time
Skills Needed
N/A
Experience Required
Minimum 2 year(s)
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