Careers

Clinical Research

 
Position:         Drug Safety / Research Associate
Department:      Consulting
Position type:    Full Time
Work schedule: Flexible within hours of operation: Monday-Friday 8am-8pm
 
Responsibilities:
  • Clinical Research: Day to day operations for all Phase IV clinical trial activities, including but not limited to: physician recruitment (telephone and fax campaigns), site management, reporting, sponsor communication, trial master file maintenance
  • Medical information: Receive and develop standard response for all medical information requests, complaints and customer service requests received via email and toll-free telephone service. Refers all non-standard response requests to Sr. Project Manager. Submits all written response for approval prior to sending to client.
  • Pharmacovigilance: Receive and document all reportable safety events in compliance with SOP/protocol and applicable legislation. Requests additional information or clarification as necessary. Submits all documented reports to responsible medical personnel and to Sr. Manager for review.
  • Work directly with external clients
  • Ad hoc support for consulting department
 
Qualifications:
  • 3-5 years experience in clinical research with safety reporting experience.
  • Min. Bachelor’s degree in related discipline or diploma in life science
  • Knowledge of all essential documents for clinical trial
  • Familiar with Canadian drug safety legislation
  • In-depth knowledge of the Microsoft Office Suite of applications
  • Familiarity with Adobe Pro, an asset
  • Bilingual, English/French preferred

How to Apply:

 
 
Thank you for your interest in Innomar Strategies. We are an equal opportunity employer