TRAINEE MEDICAL SURVEILLANCE JOBS 2022 AT IQVIA IN BANGLORE & THANE LOCATION.
ABOUT IQVIA:
IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.
JOB DETAILS:
Medical Surveillance Jobs for life science, allied health sciences, pharmacy, biochemistry, microbiology, biotechnology,nursing, biotechnology, medical laboratory sciences, physiotherapy candidates as Trainee in IQVIA. Interested and eligible candidates can apply.
QUALIFICATIONS:
High School Diploma or equivalent Life Sciences or allied health sciences,ie pharmacy, biochemistry, microbiology, biotechnology, nursing, biotechnology, medical laboratory sciences, physiotherapy
• High School Diploma or equivalent health care ie medical (allopathy, homeopathy,ayurveda), or dentistry,
PRIMARY LOCATION: Bangalore, Thane India
JOB TYPE: Full time
JOB ID: R1255427.
0 to 1 year of relevant experience.
Or 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;
JOB TYPE: Full time
JOB ID: R1255427.
JOB DESCRIPTION.
JOB OVERVIEW:
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.)
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.)
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 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.
• 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.
EXPERIENCE & SKILLS
0 to 1 year of relevant experience.
Or 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;
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