£45k - £66k per annumEstimated
...Preferred Qualifications:
If you have the following characteristics, it would be a plus:
Basic knowledge of regulatory requirements and drug development process
Scientific laboratory experience
Chromatography experience (HPLC, GC, LC/MS)
Data visualization expertise (...
Suggested
Long term contract
Local area
2 days week
3 days week
£46k - £67k per annumEstimated
...eligibility in Oncology or Hematology/Oncology desirable but not essential) required with a minimum of 8 years of post-residency experience.
Drug development experience in biotechnology or pharmaceutical industry, or a combination of academia and industry. Note: Individuals with...
Suggested
Permanent employment
For contractors
Local area
Immediate start
£24k - £32k per annumEstimated
...Preferred Qualifications:
If you have the following characteristics, it would be a plus:
Knowledge of regulatory requirements and drug development process
Scientific expertise
Chromatography expertise (HPLC, GC, LC/MS)
D ata visualization expertise (...
Suggested
Long term contract
Local area
2 days week
3 days week
GlaxoSmithKline
Brentford, Greater London
3 days ago
£39k - £57k per annumEstimated
As Scientific Director, Upstream Process Development within Biopharm Drug Substance Development, you will provide strategic leadership of scientific and organizational objectives related to portfolio projects and technology initiatives.
You’ll have the opportunity to initiate...
Suggested
Local area
£56k - £83k per annumEstimated
...end-to-end development strategies. This begins with the selection of promising candidate compounds, all the way through to late phase drug development. The team strive to use novel clinical trial designs and innovative statistical methodologies, including Bayesian techniques...
Suggested
Full time
Work at office
Local area
Remote job
Work from home
Hybrid work
£58k - £86k per annumEstimated
...compliance with regulation in all regions. Ability to recognise potential long-term issues for projects.
Experience of all phases of the drug development process in regulatory affairs
Good communication skills, especially in writing. Capable of identifying project or team...
Suggested
Long term contract
Work at office
Local area
Remote job
Hybrid work
£39k - £56k per annumEstimated
...driving record that meets Anser Advisory Requirements
Employees must complete a background investigation and successfully complete drug screenings
Must be willing to travel 1 week a month to Saudi Arabia
Full-time position based in:Philadelphia, PA, Baltimore, MD or...
Suggested
Full time
For contractors
Ongoing contract
Anser Advisory
Brentford, Greater London
4 days ago
£63k - £94k per annumEstimated
...science discipline or relevant experience.
Advanced experience in the Pharmaceutical or Biotech industry working in Pharmacovigilance, Drug Safety, Medical Affairs, or a related field.
Significant pharmacovigilance experience relating to Safety Evaluation and Risk...
Suggested
Local area
GlaxoSmithKline
Brentford, Greater London
4 days ago
£55k - £81k per annumEstimated
...the following skills are not necessary, just preferred, if you do not have them, please still apply:
Experience of all phases of the drug development process in regulatory affairs
Good communication skills, especially in writing. Capable of delivering key communications...
Suggested
Long term contract
Work at office
Local area
Remote job
Hybrid work
£30k - £47k per annumEstimated
...provided it is in their competency to do so. This includes medicines and products listed in the BNF, unlicensed medicines and all controlled drugs in schedules two – five.
What is a nurse prescriber salary in UK
The salary of a Nurse Prescriber varies depending upon the...
Suggested
Full time
Contract work
Part time
Locum
Summer work
Local area
Immediate start
Flexible hours
Shift work
Rotating shift
1 day week
Director, Senior Director & Executive Director, Safety Physician SERM (Safety Evaluation & Risk[...]
£85k - £126k per annumEstimated
...post-marketing activities
Advanced experience in the Pharmaceutical or Biotech industry working in Medical Affairs, Pharmacovigilance, Drug Safety or a related field.
An understanding of both clinical trial safety and post marketing.
Experience of working with oncology...
Suggested
Local area
