- 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.
- support on submission strategy, country requirements, etc. as well as operational support for Regulatory submission preparation and processing of amendments.
- of and input on documents related to clinical trial submissions managed by other stakeholders such as IB, Protocols.
- the approved company CTA processes are followed within agreed timelines.
- understanding of CTR process and requirements.
- key project milestones (actual vs. planned activities and timelines) and identify and communicate issues/changes to assigned stakeholders and management as agreed in company procedures.
- for all relevant databases and activity trackers are populated within agreed timelines and
- requirements met and provide operational support for Regulatory and/or non-Regulatory systems that are critical for Regulatory submission and maintenance activities.
- technical support on document preparation e.g. Excel spreadsheets, PowerPoint presentations.
- all necessary training to achieve compliance with internal/external processes.
- operational support for the CTS Team as required.
- to live and work in the United Kingdom
- Life Sciences degree or equivalent
- 12 months of previous RA experience dedicated to CTA's.
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Regulatory Affairs Coordinator - Windsor, United Kingdom - Cpl Life Sciences
Description
Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)
Job Type: 12 Month Contract
Location: Berkshire, UK – Hybrid
Rate: £22-25 per hour PAYE (inside IR35)
We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant to join on a 12-month contract basis. This role will be sat in the core regulatory CTA team and will be supporting end-to-end CTA processes. This role will support company databases and submission tracking.
This role will require the right candidates to have experience 12 to 18 months of previous RA experience ideally in clinical trials and CTR submission experience would be preferred.
Job Responsibilities include;
Candidate Requirements include;
Please note this position falls inside IR35 and has no opportunities to go through LTD, if this position is of interest to you please forward your up-to-date CV to
The role does not offer Sponsorship and needs the right candidates to be on-site 3x a week in Berkshire, UK.
