Clinical Research Scientist organise and administer clinical trials of new or current drugs in order to assess the benefits and risks of using them.
Clinical research Scientists help to organise and monitor the different phases of clinical trials of drugs.
Key responsibilities include :
Writing drug trial methodologies (procedures)
Identifying and briefing appropriate trial investigators (clinicians)
Setting up and disbanding trial study centres
Generate and QC summary tables, data listings and graphs for in-house analyses of study data or publications using standard coding practices.
Create / acquire tools to improve programming efficiency
Designing trial materials and supplying study centres with sufficient quantities
Providing clinicians with instructions on how to conduct the trials
Collecting and authenticating data collection forms (commonly known as case report forms)
Monitoring progress throughout the duration of the trial
Writing reports
Documents Required : Graduation Degree & Analytical skill Certificate
Salary Offered : 4.50 LPA
