- PW 6230 Head of Quality and Medical Excellence
This is a key, high profile role in a global Pharma company with responsibility for two key areas. This will include leading the UK GxP QMS strategy to ensure the highest standards and accurate reporting to Senior Management on the status of GxP compliance. Additionally, the role will ensure ‘Best in Class’ process improvement and Innovation for key activities across all UK Medical Functions
- Drug Safety Project Manager - UK - Global CRO
A Leading CRO is now looking to expand its already successful team with a new Drug Safety Project Manager, if you would like to take the next step in your career working with a very well established team then please see below.
- Drug Safety Physician (m/w)
Safety Physician (m/w)Office-based in Baden-WürttembergJob Description:? Medical Review - medical assessment, risk-benefit assessment and evaluation for suspected adverse events, signals and reports? Answering questions on official security-related topics? Responsibility for the safety management of clinical development products? Defining security strategy as Safety Physician for one or more assigned development projects or post-authorization studies? Preparation and review of study-related ...
- Country Study Manager
As a Country Study Manager specialising in Investigator Supported Studies (IST), you will coordinate with Global and Local Medical Affairs to ensure proposed non Roche Sponsor studies are set-up and managed, including Roche oversight of compliance to our safety reporting, finance forecasting and delivery of patients and final data to agreed milestones. ...
- Regulatory Affairs Consultant
Regulatory Affairs Consultant
Clinical Professionals are working with one of the worlds most established and well-respected contract research firms, with sites across the EMEA and Americas regions, who are looking for an experienced home-based Regulatory Affairs Consultant to join their team in Germany.
- Senior / Drug Safety Physician - 12 month contract - will consider some home / work flexibility ... Dec / Jan start ...
If you wish to apply for this role send your CV with a covering note to firstname.lastname@example.org quoting reference number noted above. Alternatively to have a confidential discussion about this or other potential roles or career options, French and German speaking candidates should call Marc Van de Voorde in our Swiss office, on +41 (0)78 170 4042 and for candidates from the UK, NL and rest of world call Mark Twigden, in the UK London office, on +44 (0)207 801 3383.
- Safety Scientist / Pharmacovigilance Scientist
I am currently recruiting on behalf of a specialist pharmacovigilance consultancy that is looking to hire multiple Safety Scientists.
- Clinical Trials Physician (m/f)
Permanent position directly at the sponsor, office based
- Lead PV Scientist - UK Pharma
A great opportunity has arisen for a Lead PV Scientist to work with a medium-sized pharmaceutical company. This is a great opening for anyone that is looking to push their career and gain some exposure in a UK Pharma.
- Consultant/Senior Consultant Regulatory Services
PAREXEL is looking for experienced Regulatory Consultants!