Hocine Ait Hamouda

Hocine Ait Hamouda

Pharmaceutical professional Seeking new opportunities in a dynamic work setting

I'm an active job seeker

Previous: Innomar Strategies, Health Canada, Algorithme Pharma


Previous: Université De Montréal



    Detail-oriented professional with over five years of experience in Pharmacovigilance, Clinical Research, Epidemiology and Public Health; Seeking new opportunities in a dynamic work setting where I can offer my skills and knowledges.


Pharmacovigilance Associate

At Innomar Strategies

From July 2016 to April 2017
Pharmacovigilance : • Track, assess, data entry into ARGUS, and follow-up on adverse drug event information for reportability to international affiliates and Health Canada meeting all compliance norms; • Review scientific literature and other sources for adverse events pertaining to company...
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Université De Montréal, Montréal

Master in Pharmaceutical Sciences, Pharmacovigilance and Risk Assessment

From September 2015 to June 2016

Research Assistant, Risk Management and Pharmacovigilance

At Health Canada

From September 2015 to April 2016
• Perform screening and review of PSURs and RMPS that involve a critical review of data from clinical studies, adverse drug reaction reports, prescription drug use data and observational studies; • Perform proactive investigation of potential safety signals (signal detection) based on information...
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Clinical Data Manager 2

At Algorithme Pharma

From March 2015 to August 2015
• Design, develop and manage clinical trial data systems, supporting materials, and processes, including the Emmes' proprietary Electronic Data Capture (EDC) system; • Develop, generate and manage data queries, reports, and other data related activities; • Manage and develop different Clinical Trial...
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Université De Montréal, Montréal

Specialized graduate diploma (D.E.S.S.) in drug product development, Pharmacoeconomics / Pharmacoepidemiology

From September 2013 to June 2015

Clinical Technician

At Algorithme Pharma

From August 2014 to February 2015
• Conducting eligibility screening, psychological assessments and interviews with volunteer participants for inclusion eligibility; • Obtaining informed consent after assessing the eligibility; • Coordinate participant tests and procedures; • Processing the required blood samples,and dispatching...
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Université De Montréal, Montréal

Master of Sciences in Pharmacology, Integrative Cardiovascular Pharmacology

From September 2011 to August 2013

Université De Montréal, Montréal

Bachelor of Science in Biochemistry, Université de Montréal

From September 2008 to July 2011


  • Adverse Drug Events
  • Argus
  • Clinical Research
  • Data Entry
  • Epidemiology
  • manage clinical trial data systems
  • Microsoft Excel
  • Microsoft PowerPoint
  • Show all skills (18)

Langues parlées


Centres d'intérêt

  • Soccer
  • Swimming
  • Tennis
  • Travelling
  • Video Games
  • Walking