Trilogy Writing & Consulting, an Indegene Company, is currently looking to hire Senior and Principal Medical Writers to support our growing company in producing regulatory documentation for the international pharmaceutical industry. At Trilogy, you will play a pivotal role in delivering comprehensive services to our clients that extend beyond writing. Our writers are integral members of clinical development teams supporting the writing and coordinating of successful documentation across a broad spectrum of therapeutic areas. As our company continues to expand, there is room to develop with us and your ideas will form our future together. For further insight into who we are and what we do, please explore our website (www.trilogywriting.com).
Trilogy offers the following:
- Competitive base salary (range: $110,000 to $149,000; the salary range is an estimate and may vary based on experience level and the Company’s compensation practices)
- Annual bonus
- A generous allowance of paid time off (vacation, holiday, birthday, illness).
- Comprehensive benefit plans to include medical, dental, vision, short- and long-term disability, life insurance with AD&D.
- 401K retirement savings plan with company match
- Full AMWA membership and annual conference attendance paid for by Trilogy
- Continuous personal and professional development opportunities
- Free weekly yoga sessions
- Other fun and exciting events to encourage team bonding and development
As a Senior/Principal Medical Writer, you will:
- Prepare a variety of clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) as the lead writer in collaboration with members of client authoring teams and supported by other writers, as appropriate.
- Ensure that all documents are produced according to agreed timelines, monitor and manage project budgets, adhere to relevant SOPs, and meet the requirements of Trilogy as well as the company’s clients.
- Be responsible for providing document-specific advice to clients.
- Oversee and coordinate other writers and QC specialists assisting on documents under your responsibility.
- Project manage the timelines and review cycles of your documents.
- Work in the client’s regulatory document management systems.
Candidates must have the following writing experience:
- At least 3 years of experience of actively writing regulatory documents.
- Worked 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.
- For the Principal Medical Writer level, experience in at least 2 different types of CTD dossiers (i.e. full new chemical entity application, a variation, a generic dossier, an orphan drug dossier, a literature-based dossier [e.g. a full-mixed application under Article 8(3) of Directive 2001/83/EC]).
- Experience interacting directly with clients or authors of the documents and coordinating review cycles, meetings, and project timelines.
- For the Principal Medical Writer level, ability and willingness to take on any project for which a Lead Writer is needed.
- Competency in the use of document management systems and review tools.
In addition to having the above writing experience, applicants must have:
- A minimum of a Bachelor’s degree in science/pharmacy (Ph.D. not necessary).
- Fluent written and spoken English skills.
- An appreciation for a well-written document and an eye for details.
- Excellent, proven interpersonal skills, and enjoy proactively participating on a team with diverse personalities.
- Flexibility and the ability to stay focused under tight timelines.
- Must live in the USA or Canada and be willing to work fully remotely or a hybrid schedule (in office/remote) from our Durham, NC, USA office.
To apply for this job please visit trilogy.bamboohr.com.
