Adverse Event Jobs in California (NOW HIRING)

Duties Help Conduct reviews and provide analysis of patient related adverse event reports. Collate, display and perform trend analysis and other statistical computation. Serve as facilitator and ...

Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...

Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...

Los Angeles, CA 90032 Duration- 4 months (Possible extension for long term) FAQ This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up ...

The Coordinator provides risk advice in a variety of areas, including consent, mandatory reporting, patient/family/visitor behavior, threat management, medication management, adverse event management ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Position Responsibilities Ensures the quality and accuracy of adverse event reports. Learns and navigates the intricacies of the BMS Drug Safety Databases to process adverse event reports. Relies ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Conduct assessments of adverse events (AEs) and complaints across multiple clinical studies, including UADE (Unanticipated Adverse Device Effect) determinations; perform complaint handling ...

Assess treatment outcomes, safety reports, adverse events, and dose escalation strategies. * Apply clinical response criteria such as RECIST, Lugano, IMWG, IWCLL, and ELN . * Provide clear, evidence ...

Assess treatment outcomes, safety reports, adverse events, and dose escalation strategies. * Apply clinical response criteria such as RECIST, Lugano, IMWG, IWCLL, and ELN . * Provide clear, evidence ...

Assess treatment outcomes, safety reports, adverse events, and dose escalation strategies. * Apply clinical response criteria such as RECIST, Lugano, IMWG, IWCLL, and ELN . * Provide clear, evidence ...

Assess treatment outcomes, safety reports, adverse events, and dose escalation strategies. * Apply clinical response criteria such as RECIST, Lugano, IMWG, IWCLL, and ELN . * Provide clear, evidence ...

... adverse event according to procedures. 5. Inform management responsible for complaint handling when information in a complaint suggests that action may be required to prevent unreasonable risk of ...

... adverse event according to procedures. 5. Inform management responsible for complaint handling when information in a complaint suggests that action may be required to prevent unreasonable risk of ...