IQVIA Released Job Openings On 11/06/2022.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 Medical Surveillance Trainee as follows.
Vacancy Details:
IQVIA Recruiting High School Diploma or equivalent Life Sciences or allied health sciences,ie pharmacy,biochemistry, microbiology, biotechnology,nursing, biotechnology, medical laboratory sciences, physiotherapy with 00-01 Years Experience for Medical Surveillance Trainee Position.Complete Details for the Medical Surveillance Trainee as follows.
Important Details :
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary:NA
- Opening date for online Application: 11/06/2022
- 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
• Under Supervision  evaluating  and analyzing  laboratory results on a daily basis,from sponsor designated central laboratory and/or data management system
• Under Supervision conduct  the monitoring of Laboratory safety parameters for each patient at every site throughout clinical drug trial
• Under Supervision conducts preliminary review of laboratory results relative to established protocol-specific reference range guidelines
• Follow established procedure for comparing current results with prior laboratory values to identify trends or potentially clinically significant increases/decreases, Under supervision, contacts the investigator site for pertinent additional clinical assessment, and consults with Sponsor/IQVIA physicians for medical evaluation of case, as needed
• Under supervision, reviews and evaluates retest results, initiates contact with investigative site, if appropriate.Composes telephone reports documenting site contact or raise queries in eDC platforms to include all clinically relevant information
• Distributes according to scheme designated at Project inception
• Attends project team meetings, as needed
• Performs other related duties as assigned.
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