Senior Clinical Research Associate

  • Via Silvio Pellico, 4, 20121 Milano MI, Italy
  • Full-time

Company Description

Founded in 1997 by two Medical Doctors , Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials.  Ergomed provides services to over 100 clients in a range of therapy areas but excels in the provision of services for  complex trials in Rare Diseases, Oncology and Neuroscience.

Job Description

Duties and Responsibilities of a Senior Monitor are:

  • Take ownership of assigned studies;
  • Carry out site selection and feasibility;
  • To act as the main point of communication with Investigator and the  team;
  • When requested to support preparation of regulatory and / or EC submission;
  • Participate in mentoring/training of new staff as well as performing co-monitoring visits, to assess junior staff performance;
  • On-Site Monitoring;
  • Performing close out visits;
  • Carrying out CTM duties when required.

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience;
  • 5 years on-site monitoring experience in phase 2/3 trials, ideally with experience of complex trials;
  • Full working proficiency in English;
  • Ability to plan, multitask and work in a dynamic team environment;
  • Communication, collaboration, and problem-solving skills;
  • Ability to travel.

Additional Information

We offer excellent chances to progress and develop. We work on a global basis on interesting projects within rare diseases, oncology, and neurology. This is an ideal position to develop a career in clinical drug development. It offers the chance to progress into clinical  team managemnet or project management.

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