IQVIA Announced Excellent Job Opportunity

IQVIA is Hiring for Centralized Monitoring Lead and has issued notification to accept Applications.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 Centralized Monitoring Lead as follows.

Vacancy summary details :

• Company Name: IQVIA
• Location : Kochi/Cochin, Mumbai, Bangalore/Bengaluru
• Post Name: Centralized Monitoring Lead
• Experience: 5 – 10 years
• No of Vacancies: NA
• Details of Salary: NA
• Closing date for online Application : Apply as soon as possible
• Date of examination: NA
• Time and Venue :NA
• Mode of application : online
• Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)
• Contact: NA

Job Description/Skills Required: 

• Manage the execution of the assigned clinical study (ies) from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and is in accordance with standard operating procedures (SOPs), policies and practices. To provide project related support and assistance across multiple projects, sites and teams and review the structured clinical data output with access to medical charts.

   

• To ensure the work is conducted as per SOPs, Policies and Good clinical practices and applicable regulatory requirements. Adherence to protocol, overall completeness, and readiness of the supplied patient information to the next level of patient review and follow the metrics and timelines.

   

• Facilitate efficient and effective review of Site Visit Reports and assure consistent standards of implementation for quality to meet or exceed quality standards. Ensure subject safety, data integrity, escalation of issues and timely and responsive feedback in compliance with IQVIA SOPs, International Conference on Harmonisation – Good Clinical Practice (ICH GCP) guidelines, protocol requirements and regulatory compliance. Develop and use of study management plans and/or risk-based monitoring specific tools and templates and/or other study specific plans to evaluate the quality and integrity of the study. 

   

• Support project management team to develop monitoring strategy including monitoring triggers/thresholds. Manage the operational insight of the assigned project(s) and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.)

   

• Essential Functions Manage assigned studies under supervision. Attend study team meetings as needed or requested.  Contribute to the development and use of study management plans and/or risk-based monitoring specific tools and templates and/or other study specific plans to evaluate the quality and integrity of the study.

   

• (CM-study/CM-subject lead) Support project management team to develop monitoring strategy including monitoring triggers/thresholds. (CM-study/CM-subject lead) Manage the operational insight of the assigned project(s) and complete the study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan,review, triage and action clinical study alerts, monitor clinical operation plan (COP) compliance etc.)Contribute to developing the study specific analytics strategy and/or work on developing advanced analytics.

How to Apply :

Step 1: Click on below link and you will be redirected to  Career Page of Recruiting Company or Career portal.

Step 2. Register on Career Page of the Company or  Career Portal by giving log in credentials and other personal or education details .

Step 3.Upon successful registration .User need to log in with credentials.

Step 4.Once logged in, User need to fill the all relevant personal ,educational  , Work experience details ,attach resume and submit application form.

Click here for notification and Apply