:::Apic world of Health Care Studies:::Kriger Research Center, Canada

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Pharma Management Course Delhi

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Address:	D-62, South Extension Part - I New Delhi - 110 049
Phone No:	011 - 24649994 , 011 - 24649965.

Kriger Research Center, Canada

Kriger Research Center Inc (KRC). is an organization with broad expertise in the planning, execution and interpretation of research projects. KRC Inc. serves as a partner in clinical research with extensive experience in different phases of clinical trials. KRC Inc. provides focused, comprehensive planning which leads to a successful trial. Beyond the trial, it is involved and committed to a development process that is custom. designed to meet it's clients' needs. It is committed to investing in ongoing training for it's employees to ensure that they are kept on the leading edge of new technologies. These training initiatives include interactions with academia, attendance at scientific conferences and meetings as well as training courses from experts in various fields, etc KRC Inc. has its Headquarters in Canada, and offices in Canada, India, Israel, Philippines, UK and USA.


Authorised Training Partner
In India Kriger Research Center, has entered into a alliance with APIC Institute of HealthCare Studies for conducting the following training programs through online & in.class modes:
Clinical Research Associate (CRA), Clinical Trial Monitoring, Site Coordination & ICH GCP Guidelines Clinical Data Management, Analysis & ICH GCP Guidelines Quality Assurance & Regulatory Affairs, ICH GMp, GLp, GCP Guidelines Management & Marketingfor the Bio Pharmaceutical Industry Clinical. Investigator Training & ICH GCP Guidelines SAS Programming Recruitment& Trainingforthe Bio Pharmaceutical Industry Medical Terminology
Career Opportunities in Clinical Research with KRC Inc.
	The students can take these on-line programs to help gain appropriate knowledge and practical skills in order to apply for the position of Clinical Research Associate/Coordinator or Data Manager/Data Coordinator and Quality Assurance Specialist. Upon completion of these programs and after passing on-line final exams the student will receive, a diploma stating his/her new qualifications. They will then be approved as a clinical research associate or data coordinator in order to participate in clinical research projects. They will be appointed to one of the on-line research groups working on a specific drug. They will receive individual clinical research and data management tasks that will give them sufficient experience to get started on their in this field. Their experience in this area will be most valuable for your future employment.
The students would actively participate in the development of some parts of the protocol, preparing CRFs (Case Report Forms), reviewing informed consent forms, networking with potential investigators, initiating clinical research sites, monitoring, creating databases, performing data entry and analysis and many other tasks. They will utilize their knowledge of ICH GCP (Good Clinical Practice) in each phase of the clinical research. At the end of their work they will receive a reference letter stating your their qualifications and experience with KRC's contract research center. At this stage one could work with KRC Inc. as a volunteer. The most successful participants could be offered employment with our Kriger Research Center Inc. upon completion of this program.

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