Clinical Research Associate (CRA)
- Full-time
- Department: Clinical Operations
Company Description
Founded in 1997 by a Medical Doctor, 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 CRA (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
- On-Site Monitoring
- Performing close out visits
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- 2 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.