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Weekend / Partime Program Starting from 10th Feb 2018
 
Professional Diploma in Clinical Trial Management, Regulatory Affairs and Pharmacovigilance
With raised standards for safety reporting and updated regulatory requirements throughout the world, excellent job opportunities are expected in India and abroad to fill forthcoming vacant positions in the companies operating in Pharmacovigilance in India and abroad. To cater to the needs of the growing industry, after placing many candidates in Clinical Research and Pharmacovigilance, Clinotek India proudly offers a dedicated program exclusively for Clinical Research and Pharmacovigilance. You can now practice your Dentistry and Medicine and also learn at the same time without quitting your current position.

Training program features:

  • Guaranteed training only by INDUSTRY EXPERTS.
  • With over 50 assignments/case studies and their detailed discussions on INDIVIDUAL CASE SAFETY REPORTS (ICSR) and AGGREGATE REPORTS.
  • The program is exclusively designed for the candidates interested in Clinical Research and Pharmacovigilance.
  • Suitable for practicing Dentists and Physicians/clinicians, working professionals in other Clinical Research domains like Clinical Trial Management and Clinical Data Management, and those pursuing their higher studies, who are aspiring to make their career in Clinical Research and Pharmacovigilance.
  • The program is developed only by industry experts considering current industry requirements.
  • All sessions will be held only by industry experts who have more than 15 years of cumulative experience in Clinical Research, Pharmacovigilance.
  • It covers lot of examples in NARRATIVE WRITING FOR INDIVIDUAL/SINGLE REPORTS.
  • Covers AGGREGATE REPORTS.
  • Covers conventions in MedDRA

Eligibility: BDS, MDS, MBBS, MD, BAMS, BHMS, B. Sc Nursing, B. Pharm, M. Pharm, Pharm. D.

Fee Structure:  Total fee of Rs. 55,000/-, to be paid in 2 installments.

First installment will be Rs. 25,000/-, payable by cash/DD/Cheque/online fund transfer. Payments through credit/debit cards are not acceptable. Rest to be paid in two more installments with one month intervals. No hidden cost.

Placement Assistance (optional) Fee: Rs. 10,000/- to be paid only after placement is confirmed by any company, after working for one month. 

Schedule:.

Duration: 4 months, weekend both Saturdays and Sundays.  4 hrs per day, in morning session (timing is flexible according to the convenience of the candidates).

On successful completion of the training, candidates are expected to be employed in entry level positions as Drug Safety Associate/ Drug Safety Physician / Associate Operations Specialist or any other designation provided by respective companies.

Companies having their Pharmacovigilance setup/outsourced activity in India are Quintiles, Accenture, Synowlegde PV Services, Cognizant Technology Services, Tata Consultancy Services, Pfizer, Merck, Johnson & Johnson, Astra Zeneca, Sanofi Aventis, Bristol Mayer Squib, Novartis, and Novo Nordisk etc.

For more information on the program:
Please call Mr. Nagendrappa. M. H, Chief Executive Officer directly on 99452 00555 or email to clinotek@gmail.com. Please visit our office at your convenient time to discuss directly with our CEO and get all your doubts clarified.

 
 
   
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