IQVIA Released Job Openings On 17/02/2022.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 Clinical Lead as follows.
Vacancy Details:
IQVIA Recruiting  Bachelor’s Degree Bachelor’s degree in clinical, life sciences, mathematical sciences, or related field, nursing qualification or allied medical degree with 05+ years of Experience for Associate Clinical Lead Position.Complete Details for the Associate Clinical Lead as follows.
Important Details :
- Location :Ahmedabad
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application:17/02/2022
- 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
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Job Description/Skills Required
• Serve as an expert on centralized monitoring studies to support from Applications, Analytics, Therapeutics, Quality perspective. Provide technical inputs in developing study specific documents, plans, applications. Provide centralized monitoring support to the relevant stake holders within the project team for assigned deliverables. Assist the relevant stake holders within the project team in developing the study management plans, tools and templates and maintain the team accountabilities as applicable. Provide resolution to the internal study team on study specific issues highlighted in the study. Provides inputs to cross functional team in managing project deliverables. Provide technical support in setting up Data analytics in the study. Support the centralized monitoring services manager in periodic review of Centralized monitoring trainings and/or identify the training needs of the team and provide inputs whenever required. Support 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. Oversee & perform trigger management compliance and i-site pack delivery. Provide technical support in conducting in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data). Conduct periodic review of site level key risk indicators and historic site performance according to Central Monitoring Plan. Early identification of site-level risk/issue(s) occurring during study conduct and responsible for identification of risk. Monitor site performance and make recommendations for timely corrective actions (e.g. Site Telephone Contact or Triggered Onsite Monitoring Visit). Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed. Review  of the Study Central Monitoring Plan.
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