Head, PV and Regulatory at Proclinical Staffing
England, London - England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

25 Nov, 26

Salary

0.0

Posted On

27 Aug, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Healthcare & Life Sciences

Description

ur Company

At Cycle, we believe that Every Single Patient Matters. This is at the heart of why we work and were looking for people to join our team who share our vision. We know that life-changing treatments need life-improving product support to match, because when you put the two together, great things can happen.

Our growing portfolio now covers oncology, haematology, neurology and rare metabolic genetic conditions where we improve existing drugs, repurpose them for new uses and bring generics back to market. Using cutting-edge drug delivery technologies, we enhance the efficiency of treatments, offering patients greater freedom and choice.

Headquartered in Cambridge, UK, with a significant US presence, Cycle has scaled rapidly and was named one of the UK’s fastest-growing private companies by The Sunday Times (Sunday Times 100 2024 & Sunday Times 100 Tech 2025). If you want to know more about what we do then, why not check out our website and take a look at some of our patient stories: Patient Stories - Cycle Pharma

What You Will Be Doing:

  • Drive the preparation and review of PADERs and other aggregate reports.
  • Ensuring that all the accountable activities are audit ready at any time.
  • Support with launch activities and preparation of regulatory dossiers from a PV perspective.
  • Review of ICSRs received from external partners prior to submission to Health Authorities.
  • Manage signal detection activities.
  • Support review and updates to relevant SOPs and WIs.
  • Developing Frequent Asked Questions lists for Cycle’s portfolio.
  • Responding to Medical Information enquiries.
  • Ensure documents shared with PV service provider remain up to date.


The following skills and experience will be important in helping you set up to succeed in this role:

  • Degree in a relevant science subject (Pharmacy, Chemistry, Biology or related discipline).
  • Previous experience working in a Pharmacovigilance role and a solid understanding of PV processes.
  • Hands on experience in writing aggregate reports (e.g. PSUR and/or PADERs) is desired.
  • Excellent communication skills and able to build strong relationships across the business.
  • Ability to work in a proactive and autonomous manner, as well as being part of a team.
  • A high level of attention to detail and quality.
  • Strong analytical, organisational and problem-solving skills.
  • Willing to learn new processes and work to procedures set within the business.
  • Proficiency with the Microsoft Office suite, including Word, Excel and PowerPoint.
  • Ability to manage a range of tasks at any one time and prioritise own workload.


How To Apply:

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Responsibilities
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