Senior/principal Medical Writer - Frankfurt am Main, Deutschland - Trilogy Writing & Consulting

Trilogy Writing & Consulting

Geprüftes Unternehmen

Frankfurt am Main, Deutschland

vor 2 Wochen

Geschrieben von:

Lena Wagner

beBee Recruiter

Beschreibung

Trilogy Writing & Consulting is currently looking to hire Senior and Principal Medical Writers (m/w/d) to support our growing company in producing high-quality 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.

Tasks

As a Senior/Principal Medical Writer (m/w/d), 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 documentspecific 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.

Requirements:

Relevant professional experience 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.
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:

Diploma/Master's/Bachelor's degree in science/pharmacy (Ph.

D. not necessary).

Fluent written and spoken English skills.
An appreciation for a wellwritten document and an eye for detail.
Excellent, proven interpersonal skills, and enjoy proactively participating on a team with diverse personalities.
Flexibility and the ability to stay focused under tight timelines.
Applicants will work from one of our offices (Frankfurt, Germany or Cambridge, UK) and can work in an officebased, hybrid, or fully remote setting. Freelancers need not apply.

Benefits:

Remuneration will be relative to the level of experience, with all standard Trilogy benefits.

Submission of documents in English:
Cover letter specifying how you comply with the experience requirements
CV

Trilogy Writing & Consulting complies with all laws respecting equal employment opportunity and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state/provincial, and local law.

We passionately believe in creating a supportive environment in which everyone can grow, flourish, and do their best work.