Senior Medical Writer

Ferring Pharmaceuticals

Kastrup, Denmark

As a Senior Medical Writer, you will be responsible for delivering submission-ready documents and take the role as lead medical writer on specific assignments. In addition, you can look forward to joining a diverse organisation shaped by cross-functional and global collaboration – and a focus on continuous transformation to support the future needs of clinical development.

Reporting to our senior director, Global Medical Writing, you will be responsible for driving and developing clinical documents regarding the planning, reporting and communication of clinical trials conducted globally by Ferring. You can look forward to writing a variety of regulatory documents, this includes (but is not limited to) outlines, protocols, amendments, IB, CTR, clinical documents for regulatory dossiers, and other ad-hoc clinical documents to support health agency interactions.

Your main responsibilities will be to:

Plan, coordinate and author the documents required for end-to-end clinical development
Support document preparation towards health agency interactions
Analyze and interpret clinical trial data together with relevant clinical team members
Participate in the project clinical development teams and clinical trial teams as a core member, and provide guidance on the regulatory requirements for the documents we deliver and best practice approach to present our data in the documents
Contribute to the optimization of our processes and procedures
Keep up to date on regulations pertaining to medical writing
Contribute to quality control within the team

We imagine that you:

Bring 3+ years of experience as a medical writer in, the pharmaceutical or the biotech industry
Have previous experience from working in a global setting and have a global mindset
Have an academic degree in life science – ideally a Ph.D. or similar
Have knowledge of clinical drug development and regulatory requirements
Have a track record of driving and setting timelines for your deliverables
Have a willingness to share from experience and improve processes in a collaborative manner
Are fluent in English – strong verbal and written skills are a given

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