...This is a full-time on-site role in Bengaluru for a Drug Safety Associate. The Drug Safety Associate will be responsible for tasks such as
~ Reviewing safety data, writing narratives, performing quality control ch...
...from innovative biotech start-ups to established pharmaceutical companies. Our products, services and solutions help bring innovative therapies to market and support the patients who depend on them. Our jobs, skills...
Designation: Trainee Research Associate
Job Location: Noida/Greater Noida
Department: Synthesis
Job Description:
Key Responsibilities:
Synthesis, purification and characterization of chemical intermediates.
Deliver small to large q...
...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 ...
...Details below-
Role-Drug Safety Associate
Exp-1 to 5 Years
Location-Thane, Mumbai
Responsibilities-
Triage and Prioritize cases
Full data entry of all relevant information from the source data
Manual coding of ...
# 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...
...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...
...timely performance are the core values of Xcene Research.
Role Description
This is a full-time on-site role for an Associate Lead Scientist - Bioanalytical. The role involves conducting bioanalytical assays, over...
...The PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety. Key Responsibilities
Independent authoring, editing and reviewing of vari...
...and the client to get the required inputs.
Perform quality review of the safety reports prepared by junior or associate medical writers.
Author or contribute to ad hoc reports, benefit-risk evaluation report...
