IQVIA is Hiring for Clinical Research Associate/Scientist 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 Clinical Research Associate/Scientist as follows.

Vacancy summary details :

Company Name: IQVIA
Location :india
Post Name: Clinical Research Associate/Scientist
Qualification: B.pharm
Experience: 3 – 8 years
No of Vacancies: 03
Details of Salary: Not Disclosed by Recruiter
Opening date for online Application: 14/02/2021
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: sheetal.jamane@iqvia.com

Job Description/Skills Required:

Oversee a caseload of SVRs for assigned studies, ensuring compliance to the protocol, processes, timelines, Quintiles/applicable SOPs, and GCP guidelines. Review SVRs to ensure findings requiring corrective and /or preventative action plans are documented and followed up to resolution, to ensure high quality reports.
Participate on the project team for all SVR review activities and identifies and escalate CRA and /or site issues, relevant trends, and related risk factors to the project team and appropriate parties in a timely manner to optimize quality of project delivery.
Provide guidance to Clinical Project Managers (CPMs) at project start-up and throughout the study and partner with the project team members to decrease the level of corrections/additions needed on reports by providing insight and training of the SVR annotations.
Identify and track the project team compliance to SOPs for submission and approval of the SVRs through communication with the CRAs and line managers.
Participate in meetings with project team to discuss any SVR review issues illustrative of
quality/performance deficiencies across PIs/sites and CRAs. Assist with identification of the trends emerging from the Issue Escalation Log.
Provide coaching to decrease the level of corrections/additions needed on reports.
Provide quality improvement support such as quality checks, data trending, providing back up support and mentoring and coaching of junior staff members.
May take on special project assignments related to function/corporate initiatives.