Degree: Life science degree expected with particular focus on virology. Coordinates the development of protocol level documents and plans.
Working for Technology Transfer documents for herbal extraction technology Extraction Process development Structure elucidation of new compounds Desired Profile M.
They should have undergone SOP training in Clinical Research along with knowledge in Standard Operating Procedures for clinical research and quality assurance.
Provide medical assessments of clinical trial and spontaneous event reports. To conduct, Monitor clinical studies as per GCP. Working for Technology Transfer documents for herbal extraction technology Extraction Process development Structure elucidation of new compounds Desired Profile M. Board certified or board eligible is preferred. Ensure regulatory compliance in respect of pharmacovigilance. Online project guidance is our main peculiarity.
Online project guidance is our main peculiarity.
Prepare reports of PMS studies for regulatory submission. The requirements for this position include: BA.
Monitoring of Adverse Events from clinical trials. Those who have interest in doing quality projects and expand their carrier growth are welcome.
This position will be responsible for production of analysis datasets and specifications, well documented code, summary tables and some statistical analysis of data.
To intimate any discrepancy in conduct of trial. Responsible for supporting pre-clinical and clinical development of HCV compounds. They should have undergone SOP training in Clinical Research along with knowledge in Standard Operating Procedures for clinical research and quality assurance. Must have experience in preparation of dossiers. Manages clinical deliverables, budgets and timelines. Manages clinical deliverables, budgets and timelines. Manages clinical staff and clinical projects, including CROs and contract labs. After the constructs are clone into the suitable vectors they are mobilised into the Agrobacterium Strain.
Make recommendations to Corporate Drug Safety Committee, as required.
Ensure that the global pharmacovigilance database is updated periodically. Working for Technology Transfer documents for herbal extraction technology Extraction Process development Structure elucidation of new compounds Desired Profile M. The requirements for this position include: BA.
Coordinates the development of protocol level documents and plans. Formulation development for cytotoxics - including intravenous formulations.
Board certified or board eligible is preferred. Then they are transform into the rice plant for the transgene _expression_ and finally their analysis. Monitors protocol progress; addresses and manages obstacles.