We are seeking a highly motivated Research Associate with experience using tissue culture and performing protein or cell-based assays, preferably in an industry setting.
SRG are working with a Global Biopharmaceutical company to help them find a Research Associate to join their busy team.
You will be responsible for performing protein and cell-based screening assays for small molecules, biologics and new therapeutic modalities.
This project aims to characterise a novel plant signalling mechanism that enables nitrogen-fixing rhizobia to successfully colonize root nodule.
The Charpentier group focuses on understanding the complex plant signalling networks that govern endosymbiotic interactions between soil microbes and crops.
Applications are invited for Postdoctoral Researcher to join the Charpentier group at the John Innes Centre (JIC).
I am currently working with a leading market research firm specializing in consumer insights and data analysis.
The ideal candidate will be responsible for conducting market research in Latvia, analyzing consumer behavior, and interpreting data to provide valuable insights to our clients.
This role is completely remote and is perfect for anybody looking for flexible hours/days.
About the Trial: Our Client is conducting a significant clinical trial to investigate the effects of oral semaglutide versus placebo on cardiovascular outcomes in up to 20,000 participants with type 2 diabetes.
Study treatments will be sent to participants' homes by post.
Participants will take part remotely by completing questionnaires on their own devices or during telephone interviews with research nurses.
I am currently working with a leading market research firm specializing in consumer insights and data analysis.
The ideal candidate will be responsible for conducting market research in the Netherlands, analyzing consumer behavior, and interpreting data to provide valuable insights to our clients.
This role is completely remote and is perfect for anybody looking for flexible hours/days.
Join our global quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards.
This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a contract basis.
The duration of the contract will be 23 months with a start date in September 2024.