
Associate Medical Data And Safety Review Director
Há 4 dias
Attend and present Medical Data Review activities during the client Kick Off Meeting Write Medical Data Review Plan in collaboration with the Medical Monitor and in accordance with the client input Create protocol specific Medical Data Review Guide in collaboration with the Medical Monitor Participate in the internal eCRF review meeting and contribute to the development of eCRF Define data capture requirements as required throughout the study that are consistent with the protocol and reporting needs Contribute to the Data Review Plan Provide requirements and specifications for programming of data listings Collaborate with Clinical Science and Data Operations teams in the development of Qlik Sense builds and protocol specific customizations for patient profiles Participate in activities involving risk assessment and measuring the effectiveness of risk minimization measures Provide medical review of data listings and patient profiles, including but not limited to, adverse events, concomitant medications, medical history, labs, vitals, ECGs, eligibility criteria, efficacy assessments and study specific assessments Prepare protocol specific templates for the periodic summary reports for safety data, including the Safety Trend Analysis Report (STAR) or Safety Review Committee slide presentations, in collaboration with the Medical Monitor Compose the STAR report during the study according to scope and timelines Conduct in-stream data trend analysis in support of data quality and integrity including protocol compliance and targeted review of patient data Prepare periodic MDR summary reports or presentations if requested Medical review and case assessment of SAEs including assessment and coding of preferred term, medical history, indications of concomitant medications and treatment medications;
determination of seriousness, causality, expectedness;
narrative review;
query generation and follow up of SAE till case closure Compose sponsor comment/summary Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements MINIMUM REQUIRED EDUCATION AND EXPERIENCE:
Medical degree from an accredited, internationally recognized medical school or if in the US, a degree from an accredited Physician Assistant or Nurse Practitioner program Recipient of a medical license from the country or region in which he/she currently resides or previously resided, or if in the US recipient of a license to practice medicine as a physician assistant or nurse practitioner 5 years' experience in the practice of medicine in a clinical or academic setting which may include specialty medical training or fellowship Minimum of 5 years' experience in Medical Data Review and Medical Safety Review IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at About the company IMS Health and Quintiles are now IQVIA. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, t... Notice Talentify is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. Talentify provides reasonable accommodations to qualified applicants with disabilities, including disabled veterans. Request assistance at or . Federal law requires every new hire to complete Form I-9 and present proof of identity and U.S. work eligibility. An Automated Employment Decision Tool (AEDT) will score your job-related skills and responses. Bias-audit & data-use details:
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