Advanced Diploma in Clinical Trial Management, Regulatory Affairs, Pharmacovigilance and
Clinical Data Management.
Batch Size: Only 10 candidates to ensure effective training thrugh individualized attention
Guaranteed Training only by Industry Experts having cumnlative experience of over 18 years.
Paying Guest (PG) accommodation facility arranged for all outstation candidates
One course, crafted according to the current Industry standards, designed to save valuable time and money. The program enables the candidate for all the three areas (as a result, 3 candidates have been employed at Accenture (one of the leading Multi Nationals) in Clinical Data Management Dept as 'Clinical Data Validators').
Schedule : Every alternate day i.e. Monday, Wednesday, Friday and Saturday
4 days a week, 4 months duration
Training Fee + Fee for full study material(Soft copy only): Rs. 70,000/- to be paid in 3 installments (includes training fee, seminars, HR Training with resume writing. No hidden cost)
You can now block the seat just by paying Rs. 10,000/-
Most Important : Practical Training will be provided by the EXPERTS in Clinical Research and Clinical Data Management industry, not from just teachers.
Admission Procedure :
For the candidates who secured 60% or more marks in their graduation/post graduation, no interview is necessary and they are allowed to register by paying a registration Fee of Rs. 25,000/- in the name of 'Clinotek India' at any branch of Axis Bank throughout India. Remaining fee can be paid in another 2 installments with one month intervals.
Placement Assistance (optional) Fee : Rs. 10,000/- to be paid only after placement is confirmed by any company.
Topics covered under Training (includes practicals with software wherever applicable) :
(Only broad headings are mentioned here. Details on the complete course will be provided to all enrolled candidates) • Drug Development Process • ICH - GCP training in detail • Clinical Trial Design • Clinical Research methodologies •Clinical Trial Management • Clinical Data Management • Pharmacovigilance • Investigational Product Management • Protocol Development, Investigator Brochure and essential documents development • Regulatory Affairs in Clinical Research for European Union and United States FDA and Schedule 'Y' regions • Clinical Data Management with software used in the industry • HR, soft skills, Resume writing with • Mock interviews from HR experts from CR industry
