Trilogy Writing & Consulting is looking to hire Senior/Principal Medical Writers to support the production of high-quality regulatory documentation for the international pharmaceutical industry. As a Senior/Principal Medical Writer, you will be responsible for preparing clinical regulatory documents, managing project timelines, and working with client teams. The company is based in Portugal and has offices in the UK, Germany, Italy, and Ireland. The ideal candidate will have several years of experience in writing regulatory documents, a diploma or degree in science or pharmacy, and fluent written and spoken English skills.
Requirements
- Several years of professional experience actively writing regulatory documents
- Experience as the lead writer on >3 (Senior Medical Writer) or >5 (Principal Medical Writer) of at least 3 of the following: Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications
- Competency in the use of document management systems and review tools
- Fluent written and spoken English skills
- Diploma/Masters/Bachelor’s degree in science/pharmacy
- Flexibility and the ability to stay focused under tight timelines
- Excellent, proven interpersonal skills and enjoy proactively participating on a team with diverse personalities
- Ability and willingness to take on any project for which a Lead Writer is needed
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Relocation Assistance
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