Careers

Clinical Research

 
BILINGUAL RESEARCH ASSOCIATE
Position type:       Full time, Permanent
Location:               Burlington, ON
Work schedule:  Flexible within hours of operation: Monday-Friday 8am-8pm
               
Great entry-level position available!
 
Reporting to the Manager, Drug Safety & Pharmacovigilance, the Research Associate is responsible for assisting with the daily operations of the department. The Research Associate is responsible for maintaining compliance with all safety legislation. As a part of the Strategic Consulting Department, this position may be required to assist with other Strategic Consulting projects on a needs basis.
 
Responsibilities include:
  • Clinical Research: Assist with day to day operations for all clinical trial activities, including but not limited to physician recruitment (telephone and fax campaigns), site management, reporting, sponsor communication, trial master file maintenance, and management of ethics approval.
  • Medical information: Respond to all requests requiring standard response related to medical information received via email and toll-free telephone service. Refer all non-standard response requests to the Manager. Submits all written response for approval prior to sending to client.
  • Pharmacovigilance: Receive, evaluate and report all adverse events and product complaints in compliance with SOP/protocol and applicable legislation.   Request additional information or clarification as necessary and report all relevant safety events to appropriate personnel and to the sponsor. Support development of Standard Operating Procedures for   management of adverse event activities and processes. Manage local adverse event files and provide regular safety updates to management; Establish working relationships with internal and external clients; Support training activities for Immomar staff on safety reporting requirements; Maintain tracking systems to support Pharmacovigilance activities; Ensure audit readiness.
  • Document management: Electronic scanning and filing of proposals, contracts, and other documents. Tracking of projects and monthly billing preparation and reconciliation. Run reports specific to reporting needs outlined by client Ad hoc support for consulting department
 
Position Requirements:
  • Bilingual, English/French.
  • Professional with a minimum of 1 years experience in the healthcare, clinical research, or equivalent and related experience in the pharmaceutical industry.
  • Bachelor of Science (B.Sc.) degree or equivalent in related discipline or diploma in life science is an asset.
  • Knowledge of all essential documents for clinical trial and familiar with GCP, ICH, FDA and TPD guidelines.
  • Understanding of Federal and Local Legislations and Guidelines relating to Adverse Drug Reporting.
  • Ability to work independently or as part of a team in a multitasking, deadline-oriented team environment.
  • Scientific and medical writing skills an asset.
  • Excellent interpersonal, communication and presentation skills.
  • Strong organization, prioritization and problem solving skills.
  • In-depth knowledge of the Microsoft Office Suite of applications.
INNOMAR OFFERS:
Growth!
Competitive Compensation & Benefits Packages!
Flexible Hours!
A Dynamic, Energetic Working Environment!
Opportunities for Advancement!

 

 

HOW TO APPLY:

 

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