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...
...clinical trial related safety exchange agreements in line with regulatory requirements and internal company SOPs.
Make presentation w.r.t safety reporting for IM or site initiation visit (SIV) as required.
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...We're seeking highly motivated and self-starting individuals to join our diverse and very engaged quality auditing team! We offer a quality auditing function, with good visibility into our Research & Development fun...
# 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...
...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 ...
...Job Overview:
We are seeking a highly skilled and detail-oriented Submission Expert specializing in Individual Case Safety Reports (ICSR) to join our Pharmacovigilance team. The Submission Expert will play a crit...
