Contribute to clinical development plans, clinical sections, stat
istical analyses plans, PK/PD analyses, clinical study
reports and review of other study related documentation (Investigators Brochure, Scientific Rationales/Justification,
Regulatory agency briefing documents and responses to questions
Developing sample prep methodology from various matrices (e.g. biological fluids, blood spots, etc.) compatible with LC-MS including protein precipitation, liquid-liquid extraction, solid phase extraction and affinity enrichment.
We are currently seeking a Clinical Research Scientist (CRS) to join our Clinical Science Department. This position will report to the Senior Clinical Research Scientist, and will support the Medical Directors, and other Clinical Development colleagues in the delivery of company objectives.
In this role, the selected candidate must have a hands-on experience using molecular biology techniques including PCR and real-time PCR to evaluate clinical samples in a hospital, CRO, reference laboratory, or similar environment.
Assists with PowerPoint training of investigative personnel on human subject protection, principal investigator obligations, GCP and local regulations to ensure sites are conducting clinical research according to protocol and regulatory requirements. Training may take place either at investigator meetings or at the investigative site.