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Sr. Clinical Research Associate (Temporary) California-San Francisco
9/18/2014 11:56 AM

The Sr. Clinical Research Associate regularly represents department in team meetings, leads teams and drive collaborative efforts (e.g., protocol development, CRO selection, etc.). RESPONSIBILITIES • Oversees and is accountable for feasibility assessments for new studies. • Responsible for TMF contents and accountable for TMF reconciliation. • Oversees and is accountable for the conten  ...View Job
Scientist I, BioAnalytical Research & Development California-San Francisco
9/15/2014 11:47 AM

Critical to the success of each new therapeutic, the BioAnalytical R&D group develops and validates novel assays to measure pharmacokinetics, immunogenicity and biomarkers. We are searching for an industry experienced Scientist I/II who will develop and execute cell-based functional assays and immunoassays using innovative new technologies. This position offers a unique career opportunity to wor  ...View Job
Principal Statistician California-San Francisco
9/8/2014 6:33 PM

SUMMARY The Principal Biostatistician II/Senior Manager of Biostatistics is a skilled Biostatistician with training and significant experience in statistics, drug development, and clinical research. This person will provide biostatistics and biometrics leadership and oversight for all phases of clinical trials and drug development programs, including regulatory submissions. This individual is als  ...View Job
Manager, QA Validation CIP/SIP California-San Francisco
9/5/2014 1:31 PM

Summary This position is responsible for all aspects related to cleaning and steam sterilization validation activities for biological manufacturing processes in a cGMP environment. This position will coordinate and manage cleaning and steaming process validation projects related to the implementation of new manufacturing processes and changes to existing processes. The position will primarily  ...View Job
PV Specialist II California-San Francisco
9/5/2014 1:12 PM

SUMMARY This Pharmacovigilance Specialist II will participates in activities related to, and reporting of Adverse Events for BioMarin post marketed products and investigational products being assessed in clinical studies. Contributes to departmental clinical study activities and risk management activities as needed. RESPONSIBLITIES • Performs triage for all incoming cases (including th  ...View Job