RESPONSIBILITES
Manage bioanalytical projects in the role of Principal Investigator or Responsi-ble Bioanalyst according to GLP or GCP regulations
Supervise the development, validation and application of LC-MS bioanalytical methods for quantification for small molecule drugs, biologics and biomarkers
Discuss analytical results internally and with clients and take ownership of the quality and integrity of the reported data.
Author, edit, and review bioanalytical protocols and reports.
Communicate relevant project details to laboratory operations in a proactive manner to ensure smooth business operations
Discuss new project opportunities and consult clients to develop optimal project designs in association with business development
Represent bioanalytical projects during client audits and health authority in-spections in association with Quality Assurance
Contribute to creation of clinical laboratory manuals
Review service estimates in knowledge of clinical study designs and translate those into adequate bioanalytical protocols