- Parexel (Salem, OR)
- …Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience: Minimum 3 years ... (DSMM) + Partners with SCP and Country Study Operations Manager (SOM) + When required Partners with other Study...relevant experience in clinical research site monitoring (preferably 2 years in… more
- Parexel (Salem, OR)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery of the ... delivery of the study. The CRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Salem, OR)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the ... delivery of the study. The SrCRA is responsible for the preparation, initiation, monitoring , and closure of assigned sites in clinical studies, in compliance… more
- Parexel (Salem, OR)
- …processing cycle + Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs) + Provide medical ... + Perform review and summarization of literature citations including epidemiology background research + Provide safety content review of clinical protocols,… more
- Parexel (Salem, OR)
- …Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to travel 15-20% is required _**Internal ... + Participate in the development and/or review of study documents, such as clinical protocols, Medical Monitoring Plans (MMP), integrated clinical and… more
- Parexel (Salem, OR)
- …work remotely. The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will ... randomization, analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents + Perform sample-size… more
- Edwards Lifesciences (Remote, OR)
- …subject documentation is within parameters of study hypothesis, as well as monitoring clinical trial/study safety, in keeping with protocols, GCP (Good ... skills. + Providing input on strategic direction on field monitoring of studies and data collection for clinical...cardiology trials + Master's Degree in related field + Clinical research certification (ACRP or SoCRA … more
- ThermoFisher Scientific (Hillsboro, OR)
- …project specifications. Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are ... Office **Job Description** Monitors investigator sites with a risk-based monitoring approach: applies root Functions cause analysis (RCA), critical thinking… more
- Merck (Salem, OR)
- …or business management is preferred. **Prerequisites:** + Minimum of 6 years in clinical research including at least 2 years with developing and managing ... up of regulatory inspections. **Operational Quality Management:** + The Clinical Quality Operations Manager is accountable for... Clinical Data Management, Clinical Development, Clinical Quality Management, Clinical Research ,… more
- Otsuka America Pharmaceutical Inc. (Salem, OR)
- …sciences or related field; advanced degree a plus. + 6-8 years of experience in clinical quality assurance or clinical research within the pharmaceutical or ... **Job Summary** The Senior Manager of Global Quality Management (GQM) supports the...of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good … more
