Senior Clinical Research Associate

  • 1601 Trapelo Rd, Waltham, MA 02451, USA
  • 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.