The UK Clinical Projects Group, within the Medical Affairs Department is a rapidly evolving team of Project Managers and Clinical Trials Assistants de...
You will apply your extensive experience in pre-launch marketing to maximise the potential value of a variety of pipeline products. You would be the ...
To further strengthen our national Regulatory Affairs group, part of the Medical Department, we have an exciting opportunity for an experienced regula...
NCR is a key member of the regulatory matrix team, acting as the regulatory specialist for all nonclinical work or issues. NCR coordinates and prepar...
A forensic scientist with DNA specialisation and court experience as an expert witness. Responsible for high throughput reporting of NDNAD matches and...
You’ll work well alongside the DMO Team Manager to ensure all tasks documented in the sponsor contract are completed on time and monitor project budge...
This is an important position, managing all the regulatory activities and packages that apply to our clinical work across a range of countries. You wi...
The successful candidate will be PMP qualified or have equivalent professional experience, preferably in a pharmaceutical organisation or CRO. A backg...
We are looking for a senior regulatory specialist to co-ordinate our clinical trial and marketing authorisations and develop regulatory packages for e...
The successful candidate will have several years’ experience in a similar position - preferably in the pharmaceutical industry - three years’ involvem...
Develop and implement the product safety strategy and overall risk/benefit assessment,
Integrate, analyse and clinically interpret safety information...
The role will require you to be medically qualified having obtained a medical degree or PhD along with a minimum of 7 years progressive experience in ...
As the Global Auditor Manager you will be joining their global operational excellence team and you will focus on Quality engineering, Global audit man...
You will have strong organisation and communication skills and a thorough understanding of medical terminology, physiology, pharmacology and the drug ...
You will have at least two years experience in a CRO, pharma/biotech outsourcing or software company in a similar role. A Bachelors degree in a busine...
The FSE will act as an essential interface between the field organization and internal support structure by providing timely onsite technical assistan...
The GPM will be responsible for managing International studies in Phases I-IV. This is a client focused role which is pivotal in the success of our pr...
The successful candidate will be expected to know Allergan systems and SOPs to a good level, and really focus on CRA performance / generate metrics /...