Medical Writer and Project Coordinator (full-time / part-time) in Darmstadt bei Merck KGaA

Medical Writer and Project Coordinator (all genders) (full-time / part-time) in Darmstadt bei Merck KGaA

Merck KGaA

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know youâ€™ve got big plans â€“ so do we! Our colleagues across the globe love innovating with science and technology to enrich peopleâ€™s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your role:

In your role you will dedicate 50% of your time for Medical Writing and 50% of your time for Project Coordination.

You will serve as a scientific publication specialist within the Research Unit Oncology, providing assistance on slide decks and documents for external scientific presenatations at e.g. scientific conferences. Furthermore, you will be responsible for Scientific Competitive Intelligence and Publication Management incl. scientific writing. You will write, co-write, and edit IND documents for oncology assets, create and format documents within the regulatory document management system, also involving setting up and managing workflows, and performing internal quality control checks on documents.

In your project coordination role you will support the department setting up and managing (master) service and license agreements incl. but not limited to cell line MTAs and license agreements in close collaboration with the relevant interfaces (e.g. Legal, Patents, Procurement). You will further manage on-going cross-functional relationships with external service providers and support out colleagues with contractual matters related to student visits and internships. You will work in close collaboration with the department's Scientific Collaboration Manager with regards to contracting-related matters providing ad-hoc support when applicable.

Who you are:

Bachelor's or Master's degree in Life Sciences or similar
>1-2 years of biopharmaceutical industry experience
In depth multidisciplinary scientific and technical background with strong focus on oncology
Ability to structure complex processes and projects and stay on top of a multitude of parallel interactions and activities
Have an eye for detail and accuracy
Track record for Medical Writing an publication writing experience
Ability to work independently & in a team, while being able to step aside and allow the necessary room for the content and the partner
Affinity for legal language is required
Outstanding verbal and written communication and presentation skills in English are required, German knowledge as an additional asset
Well-versed in MS Office 365 applications

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of our diverse team!