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Remote Site Monitor

PPD - Pharmaceutical Product Development

Milan, Italy

Responsibilities:

  • Performs remote site management activities on assigned project(s) in accordance with FDA and/or local regulations and guidelines, ICH GCPs and PPD procedural documents;
  • Reviews study data from various sources remotely;
  • Contacts study sites to collect study documentation, resolves issues and requests outstanding information.

Education and Experience:

  • Bachelor’s Degree in a life science-related field;

Knowledge, Skills and Abilities:

  • Basic medical/therapeutic area knowledge and understanding of medical terminology;
  • Ability to attain and maintain a working knowledge of FDA and/or local regulation and guidelines, ICH GCPs and PPD procedural documents;
  • Ability to successfully complete PPD’s Clinical Foundation Training Program (CFP);
  • Ability to evaluate medical research data;
  • Ability to advise, counsel, and motivate investigational sites;
  • Effective oral and written communication skills with the ability to communicate effectively with medical personnel;
  • Excellent interpersonal and customer service skills;
  • Good organizational and time management skills;
  • Proven flexibility and adaptability;
  • Strong attention to detail;
  • Ability to work in a team or independently, as required;
  • Good computer skills with good knowledge of MS Office (Word, Excel, PowerPoint) and the ability to learn appropriate software;
  • Ability to extract pertinent information from all study documents, such as protocols, electronic study data systems, CTMS and dashboards;
  • Excellent English language and grammar skills;
  • We are looking for candidates who have a Ministerial Decree/Certificate to monitor in a CRO.

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