- Parexel (Santa Fe, NM)
- …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 (Santa Fe, NM)
- …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 (Santa Fe, NM)
- 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 (Santa Fe, NM)
- …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 (Santa Fe, NM)
- …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 (Santa Fe, NM)
- …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 (Santa Fe, NM)
- …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
- Merck (Santa Fe, NM)
- …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. (Santa Fe, NM)
- …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
- Parexel (Santa Fe, NM)
- …or equivalent. + **Experience:** 3-5 years of relevant industry experience ( clinical research , feasibility, site engagement, project coordination, or related ... **PXL FSP - Join an organization shaping smarter, faster clinical development** PXL FSP is seeking a detail‑oriented and proactive **Feasibility Study Manager **… more
