Trainee Graduate Medical Writer
ESPL Regulatory Consulting
ESPL is an employee-owned international regulatory consultancy based in Shetland. We support pharmaceutical / medical device companies across Europe, the US and other world markets with developing and licensing innovative new products and technologies across a range of medical conditions. Our enthusiastic and diverse team are looking for a recent / upcoming science graduate to train as a medical writer, preparing and reviewing applications to regulatory agencies.
This full-time role will involve:
- Training with an experienced medical writer to learn the skills of collating and preparing summaries of non-clinical and clinical data in support of new applications.
- The review and development of medical writing procedures within the company.
- Active participation in negotiations with Medicines and Medical Device Regulatory Agencies globally.
Skills required:
- An eye for detail and good critical thinking skills
- Good communication and time management skills
- Ability to present data / information in a compelling way
Some familiarity with literature searching would be helpful, but is not essential, as training will be given.
Initially this will be a 1-year contract, based in Shetland, with the potential for conversion to a permanent role and career progression for the right candidate.
If you are interested, or curious to know more, please contact/send your CV to: smt@espl-regulatory.com.
Closing date for applications: 31st July 2024.