-
Regulatory Affairs Coordinator
1 day ago
Cpl Life Sciences Marlow, United KingdomJob Description · Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) · Job Type: 12 Month Contract · Location: Berkshire, UK – Hybrid · Rate: £25 to £35 per hour PAYE (inside IR35) · We are partnered with a leading Pharmaceutical organisation who are looking for a ...
-
Regulatory Affairs Coordinator
6 days ago
Cpl Life Sciences Marlow, Buckinghamshire, United KingdomJob Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) · Job Type: 12 Month Contract · Location: Berkshire, UK – Hybrid · Rate: £25 to £35 per hour PAYE (inside IR35) · We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulato ...
-
Regulatory Affairs Coordinator
1 week ago
Cpl Life Sciences Marlow, Buckinghamshire, United KingdomJob Title: Regulatory Affairs Coordinator CTA, CTR (Consultant)Job Type: 12 Month Contract Location: Berkshire, UK – Hybrid Rate: £25 to £35 per hour PAYE (inside IR35)We are partnered with a leading Pharmaceutical organisation who are looking for a junior Regulatory Consultant t ...
-
Associate Director, Global Medical Affairs
5 days ago
ABBVIE Marlow, United KingdomProvides specialist medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (Payers, Patients, Prescribers, and Providers); generation of clinical and scientific data (enhancing therap ...
-
Compliance & Training Co-ordinator
6 days ago
Cpl Life Sciences Marlow, Buckinghamshire, United KingdomJob Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) Job Type: 12 Month Contract · 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 jo ...
-
Compliance & Training Co-ordinator
1 week ago
Cpl Life Sciences Marlow, Buckinghamshire, United KingdomJob Description Job Title: Regulatory Affairs Coordinator CTA, CTR (Consultant) · Job Type: 12 Month Contract · 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 Regulator ...
-
RPMGlobal Marlow, Buckinghamshire, United KingdomSenior Director, Regional Medical Lead, International, Pompe Location Marlow, UK Requisition ID 2251 # of openings 1 · Senior Director, Regional Medical Lead, International, Pompe · SUMMARY OF POSITION · Amicus Therapeutics is a global, patient-dedicated biotechnology comp ...
-
Compliance & Training Co-ordinator
1 week ago
Cpl Life Sciences Marlow, Buckinghamshire, United KingdomJob 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 jo ...
-
Complaints Intake Analyst
1 week ago
SRG Marlow, Buckinghamshire, United KingdomRole: Complaint Intake Analyst · Contract: 12 months · Office- Marlow (Hybrid - 3 days on site) · Pay: circa 28k p/a · Must speak a European language in addiotnal to English Purpose: · The Complaint Intake Analyst works to support PMQA through providing the initial triaging of co ...
Regulatory Affairs Coordinator - Marlow, Buckinghamshire, 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; 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 and input on documents related to clinical trial submissions managed by other stakeholders such as IB, approved company CTA processes are followed within agreed timelines.understanding of CTR process and project milestones (actual vs. planned activities and timelines) and identify and communicate issues/changes to assigned stakeholders and management as agreed in company all relevant databases and activity trackers are populated within agreed timelines andrequirements 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 necessary training to achieve compliance with internal/external processes.operational support for the CTS Team as required.Candidate Requirements include; to live and work in the United KingdomLife Sciences degree or equivalent12 months of previous RA experience dedicated to CTA's.
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 lucy.comThe role does not offer Sponsorship and needs the right candidates to be on-site 3x a week in Berkshire, UK.
