| Resume alert | Resumes 51 - 60 of 7566 |
Process Improvement Program Manager
Birmingham, AL
... brochures, recruitment materials, safety reports and submission of all forms required for active clinical drug trials - both Industry and Investigator Initiated trials - from time of site selection through closure of trial and archival of materials. ... - Apr 17
... brochures, recruitment materials, safety reports and submission of all forms required for active clinical drug trials - both Industry and Investigator Initiated trials - from time of site selection through closure of trial and archival of materials. ... - Apr 17
Data Engineer Big
Annandale, VA
... 2022 SENIOR DATA ENGINEER • Collaborated with data architects in optimizing data warehousing solution using Snowflake(MPP platform) streamlined data flows, saving 30+ TB monthly storage cost and supporting real-time analytics of clinical trial data. ... - Apr 17
... 2022 SENIOR DATA ENGINEER • Collaborated with data architects in optimizing data warehousing solution using Snowflake(MPP platform) streamlined data flows, saving 30+ TB monthly storage cost and supporting real-time analytics of clinical trial data. ... - Apr 17
Quality Assurance Team Lead
Houston, TX
... Worked on the various clinical pathways, guidelines and KPI to achieve a compliance rate of > 80%. Participated in hospital ... (ASCOT TRIAL) 6.. I-PREFER STUDY: a prospective study of prevalence of diastolic heart failure. SPECIALITY CERTIFICATIONS: ... - Apr 17
... Worked on the various clinical pathways, guidelines and KPI to achieve a compliance rate of > 80%. Participated in hospital ... (ASCOT TRIAL) 6.. I-PREFER STUDY: a prospective study of prevalence of diastolic heart failure. SPECIALITY CERTIFICATIONS: ... - Apr 17
Clinical Research Patient Care
Stockton, CA
... training in clinical research and certification as a Clinical Research Analyst Lab Technician. Proficient in ICH GCP guidelines, FDA Regulations, and Data Management, with expertise in the Informed Consent Process and Clinical Trial Operations ... - Apr 17
... training in clinical research and certification as a Clinical Research Analyst Lab Technician. Proficient in ICH GCP guidelines, FDA Regulations, and Data Management, with expertise in the Informed Consent Process and Clinical Trial Operations ... - Apr 17
Clinical Research Registered Nurse
Pilot Point, TX, 76258
... diverse clinical settings, including Investigative Site, CRO, and Sponsor. Adept in navigating the intersection of healthcare practice and clinical research. Demonstrated expertise in ICH-GCP, HIPAA, FDA regulations, study start-up, clinical trial ... - Apr 16
... diverse clinical settings, including Investigative Site, CRO, and Sponsor. Adept in navigating the intersection of healthcare practice and clinical research. Demonstrated expertise in ICH-GCP, HIPAA, FDA regulations, study start-up, clinical trial ... - Apr 16
Statistical Programming Programmer
Chino Hills, CA
... (2)Providing leadership and/or support for creating and maintaining programs to analyze and report trial data. (3 ... Processing clinical data required for analysis of clinical trials for marketed products, or for the production of safety ... - Apr 16
... (2)Providing leadership and/or support for creating and maintaining programs to analyze and report trial data. (3 ... Processing clinical data required for analysis of clinical trials for marketed products, or for the production of safety ... - Apr 16
Development Operations Clinical
Jersey City, NJ
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
... Skilled in leading cross-functional product development programs and Clinical trial team management, specifically developing and implementing strategic product development plans, and ensuring compliance with FDA regulations and ICH guidelines. ... - Apr 16
Customer Service United States
San Francisco, CA
... • Biosample Operations Specialist Verily Life Sciences South San Francisco November 2019 - May 2020 • Managed logistics for a 5-year, 2,500-participant longitudinal clinical trial, overseeing nearly 3 million samples and achieving a $250,000 cost ... - Apr 16
... • Biosample Operations Specialist Verily Life Sciences South San Francisco November 2019 - May 2020 • Managed logistics for a 5-year, 2,500-participant longitudinal clinical trial, overseeing nearly 3 million samples and achieving a $250,000 cost ... - Apr 16
Clinical Trials Trial
Temecula, CA
... Research Professional with extensive experience in Clinical Trials, Phases I-IV. Adept at supporting the administration and progress of clinical trials under the guidance of the study team including trial administrative functions to ensure relevant ... - Apr 15
... Research Professional with extensive experience in Clinical Trials, Phases I-IV. Adept at supporting the administration and progress of clinical trials under the guidance of the study team including trial administrative functions to ensure relevant ... - Apr 15
Scrum Master Product Manager
The Hammocks, FL, 33186
... ● Helping with delivery of website on time and within budget, meeting all project goals and exceeding stakeholder expectations Jun 2009 - Oct 2012 Piedmont Hospital USA Project Lead • Kept patient care protocols and clinical trial operations in ... - Apr 15
... ● Helping with delivery of website on time and within budget, meeting all project goals and exceeding stakeholder expectations Jun 2009 - Oct 2012 Piedmont Hospital USA Project Lead • Kept patient care protocols and clinical trial operations in ... - Apr 15