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Tag Archives: Diploma Program in Clinical Research

March 23, 2018

Post type:-Diploma

The Clinical Research, Drug Safety and Pharmacovigilance Diploma program is designed to develop specialized knowledge and skills required to design and write study protocols, monitor and manage clinical trials and to conduct drug safety and Pharmacovigilance activities including adverse reaction reporting and preparing periodic safety update reports.  The program focuses on the global healthcare system as well as the Canadian healthcare system, Canadian regulatory agencies.

Careers in the field of Clinical Research and Pharmacovigilance:

  • Clinical Research Coordinator
  • Pharmacovigilance data management Associate
  • Clinical Research Associate
  • Pharmacovigilance Associate
  • Clinical Data Management Associate
  • Clinical Research Project Leader
  • Pharmacovigilance Project leader
  • Clinical Research Monitor
  • Medical Information Associate
  • Pharmacovigilance Officer
  • Quality Control in Clinical Research
  • Quality Assurance in Clinical Research
  • Quality Assurance in Pharmacovigilance
  • Auditor in Clinical Research and Pharmacovigilance

For more information please visit program website

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March 23, 2018

Post type:-Diploma

The demand has never been greater for professionals who can help companies ensure compliance with applicable laws and regulations in the development and commercialization of new drugs and healthcare products. The Clinical Research, Pharmacovigilance and Regulatory Affairs program will provide you with knowledge and insight into the most recent developments in the clinical research, pharmacovigilance and regulatory affairs field.

careers in the field of Clinical Research and Pharmacovigilance:

  • Clinical Research Coordinator
  • Pharmacovigilance data management Associate
  • Clinical Research Associate
  • Pharmacovigilance Associate
  • Clinical Data Management Associate
  • Clinical Research Project Leader
  • Pharmacovigilance Project leader
  • Clinical Research Monitor
  • Medical Information Associate
  • Pharmacovigilance Officer
  • Quality Control in Clinical Research
  • Quality Assurance in Clinical Research
  • Quality Assurance in Pharmacovigilance
  • Auditor in Clinical Research and Pharmacovigilance

Requirements:-

  • Hold a degree in “Clinical Research” from an Associate, Undergraduate, or Graduate Degree Program AND
  • Have completed a minimum of one year of full-time experience (or 1,750 hours part-time) during the past two years as a Clinical Research Professional

For more information please check here

Please visit program website

Let us know your academic interests so that we can search & post programs matching your profile and interests.

Register Now  for free.