IQVIA Freshers Job – Medical Surveillance Trainee Post Vacancy
B Pharma job opening. Iqvia invites postgraduate pharma candidates for the post of Medical Surveillance Trainee. Pharma consultant vacancy. Pharma job opening at Iqvia. Iqvia M Pharma job opening 2021. Pharmacy jobs. Check out all the details on our website Rasayanika.com
Under supervision, Support Medical Surveillance Specialist to provide a wide range of medical surveillance support (including monitoring of clinical laboratory data for subjects in clinical studies and composing medical narratives, and interfacing with investigator sites.)
Job Title: Medical Surveillance Trainee
Primary Location: Bangalore, India
Full time R1234787
Eligibility Criteria:
• High School Diploma or allied health sciences,ie pharmacy,
• High School Diploma or equivalent health care ie medical (allopathy, homeopathy, Ayurveda), or dentistry,
• 0 to 1 year of relevant experience.
• equivalent combination of education, training and experience.
• “Knowledge of medical/scientific terminology;
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Ability to work independently and within a matrix team environment required;
• Ability to handle management and/or personnel issues of low complexity;
• Must have strong written and verbal communication skills; Effective skill in using MS Office applications, i.e. Outlook, Word
, Excel,• Strong technical ability to comprehend and integrate scientific data from a
variety of sources;
Essential Functions
• 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 a 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 the case, as needed
• Under supervision, reviews and evaluates retest results, initiates contact with the 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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