IQVIA Released Job Openings On 01/10/2022.The Company offers commercial, physical, and biological research and development services, as well as value-based analyses, research studies, clinical management analytics, and health outcome optimization services.Application form link provided at the end of post. Eligibility for the Associate Medical Data Review Manager as follows.
Vacancy Details:
IQVIA Recruiting MBBS/MD Graduates with 05+ Years Experience for Associate Medical Data Review Manager Position.Complete Details for the Associate Medical Data Review Manager as follows.
Important Details :
- Location : India Remote
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: NA
- Opening date for online Application: 01/10/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job: Email Resume : Cognizant Hiring B.Pharma,M.Pharma,B.Sc,M.Sc FRESHERS
Job Description/Skills Required
Provide expert skills as part of a Medical Data Review team to provide efficient, quality Medical Data Review products that meet customer needs. RESPONSIBILITIES • Serve as a Subject level Data reviewer (SLDR) and Identify any anomalies in patient reported data by performing Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy • Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data) • Provide project management to the team in the area of Project Management and viewed as an expert in data management. • Drive the delivery of end-to-end study data quality and integrity. • Provide medical, clinical, and scientific advisory expertise. • May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings. • Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. . • Define data capture requirements in line with protocol and reporting needs. • Maintain strong customer relationships • With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions • Ensure timely follow-up and resolution of compliance issues • Serve as Subject Matter Expert (SME) • Serve as POC/ Back-up POC • Continuously look for opportunities to improve efficiency of tasks and quality of deliverables Provide therapeutic area/indication training for the project clinical team. • Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
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