...The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge ...
ProPharma Group is looking for Pharmacovigilance Scientist, Aggregate Reports to join our dynamic team and embark on a rewarding career journey
A Pharmacovigilance Scientist specializing in Aggregate Reports plays a cruci...
...that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance... ...their implementation; recommends improvement plan...
The Lead pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical termi...
...Analyzes, reviews, and interprets safety data, both non-clinical and clinical.
Performs medical review of ICSRs, and other drug safety information from multiple sources, including clinical trials, spontaneous and...
# Analyzes, reviews, and interprets safety data, both non-clinical and clinical and any other relevant sources
# Authoring and review of Aggregate reports (PSURs/PBRERs, PADERs/Annual Reports/ ACO/ DSUR) for submission to local and other Health Au...
...Analyzes, reviews, and interprets safety data, both non-clinical and clinical.
Performs medical review of ICSRs, and other drug safety information from multiple sources,
including clinical trials, spontaneous ...
...from a training institute or university is desirable.
PREFERRED QUALIFICATIONS:
· Master's degree in Pharmacy, Life Science, Nursing, or a related field.
· Proven experience in training and development, q...
...pharmaceutical drugs undergoing clinical trials or once they are in the market. Using standard guidelines, they determine whether the medication causes any adverse reactions in patients and report their findings bac...
...Analyzes, reviews, and interprets safety data, both non-clinical and clinical, literature and any other relevant sources
Responsible for performing end to end case processing of Individual case safety reports to ...
