- Regulatory Project Manager\ Associate Director
Regulatory Project Manager\ Associate Director: Oxfordshire. Are you looking to work for an innovative Biotech company focused on the development of novel medicines?
- Interim Regulatory Affairs Manager
Interim Regulatory Affairs Manager
Would you like to work on innovative products which make a difference to people living all around the world?
- Clinical Programme Manager - Biopharmaceutical sector - South East - £55k to £70k - Flexibility working from home
A specialist publicly-listed biopharmaceutical company based in the South East just under 10 years ago is looking to appoint a Clinical Programme Manager to cover a portfolio of studies. Flexibility working from home can be entertained and a negotiable salary in the £55,000 to £65,000 region is on offer.
- Junior Project Manager / Study Management Associate - Pharma
Junior Project Manager / Study Management Associate - Pharma - UK (Buckinghamshire) My client is a global Pharmaceutical company who are urgently looking for a Junior Project Manager / Study Management Associate to join their team on a permanent. Ideally you will have a proven track record as a CRA / Senior CRA. You must be site based in the Buckinghamshire office. ...
- Freelance Global Project Manager – Oncology – Home Based
ROLE TITLEFreelance Global Project Manager – Oncology – Home BasedROLE OVERVIEWA global CRO, recognised as a preferred supplier within the global pharmaceutical industry are in search of an experienced clinical project manager to take the lead on global oncology projects.ROLE DESCRIPTIONThis is a truly full service role. You will hit the ground running and be expected to lead cross functional project teams. You will also be managing large budgets and liaising with clients directly. ...
- OPTION Belgium * * * Global Regulatory Leader for major biotechnology company *** Beat the downturn***high salaries plus relocation
OPTION Belgium * * * Global Regulatory Leader for major biotechnology company *** Beat the downturn, low tax rate and high salaries plus relocation There are three good reasons to consider this opportunity are in the advert, please click to read more. To apply for this position please contact me, Matt Greig or Theo Moore on +44(0)207 801 3384 or by email to Theo@advregulatory.com also I can be contact out of working hours seven days a week on +44 (0) 7918 195 166
- Regulatory Affairs Officer/RA Officer
An exciting opportunity has arisen to join a world leading pharmaceutical company, as a Regulatory Affairs Officer. Based in the South East, the company has a reputation for delivering innovative products across a range of therapeutic areas.
- PW 6374 Data Manager
A rare opportunity to take existing life science data entry experience and forge a career in Data Management. Our Client, an exciting independent Data Consultancy, requires someone to join their Information Specialist Team. Responsibility is project based and looking at top line data, identifying anomalies, cleaning the data whilst ensuring accuracy and efficiency. The role is office based and offers an exceptional working environment.
- Regulatory Labelling Manager
This Regulatory Labelling Manager job is an excellent opportunity to work for a global leader in biopharmaceuticals located in South East of England in Surrey. The company has been established for more than 150 years and is a major supplier to the NHS. This is a 12 month contract role with the possibility of an extension. ...
- PW 6351 Validation Manager
Opportunity to join this unique organisation as Validation Manager. Responsibilities include the development, implementation and management of the global validation strategy. You’ll be the point of leadership for validation practitioners and provide education, operational support and knowledge management. The role is office based from our client’s global HQ. .