OVERVIEW
The Manager, Statistical Programming is operationally responsible to ensure the direction, planning and execution of the work of the statistical programming team. The Manager, Statistical Programming provides project leadership and progr...
...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...
...As the Senior Biostatistician, you will work closely with the Lead Statistician and provide support for statistical analysis, reporting, and statistical programming specific activities which may include development ...
...Process.
Cognitive abilities including verbal reasoning, attention to detail, and critical and analytical thinking.
Good knowledge on therapy area/medical terminology.
Good comprehension skills.
Good communication (...
Knowledge of SQL Loader and best practices for loading data from flat files and different types of indexes.
Knowledge in Clinical domain, Clinical data model, and Life Sciences standards like CDISC. Basic understanding of MedDRA and WHODrug dicti...
...Department :Global Safety.
Does your motivation come from challenges and working
in a dynamic environment? Do you thrive in a working
environment where close collaboration with key...
