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  Testimonials
Testimonial Mr. Arvind : I was searching for a Clinical
Research institute, and in this search I came across CLINOTEK...
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Testimonial Dr.Sneha : After completing my BDS from
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Regular Courses
 
Advanced Diploma in Clinical Research, Pharmacovigilance, Medical Writing and
Clinical Data Management with SAS base.
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Batch Size: Only 20 candidates
Paying Guest (PG) accommodation facility arranged for all outstation candidates
Guaranteed Training through Industry Experts


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').

For the first time in the country, study material of a set of books with 5 titles from Thomson Centerwatch, Boston, USA worth Rs. 18,500/- will be given to all the candidates at no extra cost.

Schedule : Every alternate day i.e. Monday, Wednesday, Friday and Saturday
3-4 days a week, 4 months duration

Tuition Fee : Rs. 96,000/- to be paid in 4 installments (includes training fee, study material from Thomson Centrewatch, seminars, HR Training with resume writing. No hidden cost)

Placement Fee : Rs. 15,000/- to be paid only after placement is confirmed by any company, after working for one month.

Most Important : Practical Training will be provided by the EXPERTS in Clinical Research and Clinical Data Management industry, not from just teachers

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
Scientific Writing
Medical Writing
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
SAS base
HR, soft skills, Resume writing with
Mock interviews from HR experts from CR industry
 
 
   
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