Here you will find more information about a few candidates we represent. These candidates are actively seeking a new position. Of course, this is just a sample of the many candidates we represent.
If you would like information about these candidates or other candidates we represent, please do not hesitate to contact us. We will be happy to answer any questions you may have.
SENIOR SCIENTIST
A talented PhD who has eight years assay development experience with large pharmaceutical company. This candidate has extensive experience in cloning and expression of mammalian proteins, and implementing these protein products in developing assays for HTS measuring protein-protein, protein-ligand, enzymatic and other events. Assay development experience includes GLP techniques directed toward therapeutic discovery in a milestone driven environment.
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This PhD has over 10 years of experience in the pharmaceutical industry and the demonstrated ability to move small molecules from the stage of initial leads to clinical candidates. This candidate leads a team of pharmacologists in the evaluation of novel small-molecule drug candidates.
This candidate holds an MS in Packaging and has over 8 years of pharmaceutical packaging experience. This candidate has direct experience with primary and secondary pharmaceutical packaging components, packaging material and characteristics, packaging validation, secondary packaging equipment and also cGMP operations. This candidate also has knowledge of aseptic fill operations and parenteral products.
This Regulatory Manager's qualifications include an MS in a scientific discipline and 5 years experience in regulatory affairs including three years in management and two years in a pharmaceutical environment. This candidate also has experience with new chemical entities and biological products as well as experience with CDER, CBER, CDRH and international authorities.
This candidate holds a PhD in Statistics and has 10 years of pharmaceutical industry experience. This Biostatistician has experience with regulatory submissions, project and proposal management, SAS and targeted therapeutic experience.