Key Responsibilities:
. Perform accurate and consistent coding of adverse events, medical history, and drug-related information using MedDRA and WHODrug dictionaries and standard coding guidelines.
. Stay updated on the latest versions of MedD...
...Perform medical coding of clinical data such as adverse events, concomitant medications, and medical history using MedDRA and WHODrug global dictionaries as per agreed coding guidelines. This includes reviewing of a...
...The Medical Coder is responsible for performing centralized medical coding activities and serious adverse event reconciliation.
Key Tasks & Responsibilities:
Review eCRF design for appropriate capture of co...
...Act as the analyst for Non-Interventional Studies (NIS)
Contribute to the writing of the standard NIS documents (including protocol development... ...of team goals
Participate in the as...
Perform duplicate search, intake, and triage of the received source documents such as Spontaneous, Literature, Regulatory and clinical trials as per agreed timelines.
Possess thorough knowledge of regulatory updates.
Awareness and understandin...
• Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standard
coding dictionaries (MedDRA, WhoDrug) in line with global and therapeutic area guidelines.
• In collaboration with Global Data Manager, ...
Role :
Medical Reviewer
Exp :
2 years to 3 years of exp in Pharmacovigilance/ Clinical Experience.
Location :
Mumbai
Qualification
: MBBS/ MD
Job Description:
Medical review of non-serious and serio...
...Interfaces:
Global Dictionary Management, IDAR, Clinical Teams, Data Standards, Data handling, EBIS, programming, biostatisticians, medical writing, DM CRO’s and coding system vendors
Education and Experience ...
...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 ...
