Solids and liquid dosage form experince.
They should have undergone SOP training in Clinical Research along with knowledge in Standard Operating Procedures for clinical research and quality assurance. Working for Technology Transfer documents for herbal extraction technology Extraction Process development Structure elucidation of new compounds Desired Profile M.
To fill up CRF on day of recruitment and follow up.
A HO licence is preferred. Provide pharmacovigilance input on designated products, including signal detection and monitoring, formulation and preparation of ad hoc regulatory responses.
Responsible for planning, designing and executing clinical protocols supporting a specific therapeutic such as Oncology, Cardiology, Rheumatology or Neurology.
Interprets and prepares virology data for regulatory submissions. Make recommendations to Corporate Drug Safety Committee, as required. Board certified or board eligible is preferred. Field staff Training.
Apply results to bug tracking system.
D in pharmaceutical sciences. Pharma with experience in a similar field. The candidate will also perform blood processing experiments using microfluidic systems and analyze data. Pharma in Pharmaceutical Chemistry.
Review AE data, PSUR reports and PMS reports.
The candidate will also perform blood processing experiments using microfluidic systems and analyze data. Monitoring of Adverse Events from clinical trials.
Working for Technology Transfer documents for herbal extraction technology Extraction Process development Structure elucidation of new compounds Desired Profile M. A HO licence is preferred.
Monitoring of Adverse Events from clinical trials.
To fill up CRF on day of recruitment and follow up. The successful applicant will be involved in association analysis of candidate genes.