Senior Medical Writer

WHO WE ARE ☝

We are Kintiga (formerly MAP Patient Access, Axtalis, and SKC), a pan-European specialist consultancy that partners with ambitious health technology developers through the complex journey to achieve successful market access across Europe, with our tailored approach, global perspective and local expertise. 

WHAT WE'RE LOOKING FOR 🔍

As Senior Medical Writer at Kintiga, you will take on a leading role in the content and organizational delivery of market access projects. You will act as a key contact for clients, manage timelines and resources, and contribute to the strategic direction and quality of projects. In addition, you will support team development through coaching, training, and the continuous advancement of methods and best practices, thereby helping to drive sustainable project success and organizational growth.

KEY RESPONSIBILITIES ARE:

• Act as end‑to‑end Project Lead / Product Owner, ensuring high-quality delivery across content, timelines, risks, budgets, and cross-functional workstreams


• Develop and execute medical and market access strategies, including HTA dossier strategy, market access risk assessments, and strategic positioning for price negotiations


• Lead G‑BA advice meetings, Joint Scientific Consultations (JSC), and the development, preparation, and submission of AMNOG and JCA dossiers in close collaboration with clients


• Collaborate in and promote interdisciplinary, agile teams, applying modern working methods and driving continuous improvement


• Support business development activities, including proposal development and opportunity identification


• Actively contribute to knowledge sharing, internal capability building, mentoring, and cultural development

ABOUT YOU 🚀 

• Master’s degree in life sciences, medicine, pharmacy, health economics, or a related field


• 1–3 years of professional experience in the pharmaceutical industry and/or market access or management consulting


• Good knowledge of the German healthcare system and the AMNOG process, including experience with benefit dossiers


• Strong skills in scientific literature research and medical writing


• Experience in project management, as well as conducting and moderating trainings and workshops


• Native German and excellent English language skills (C2), both written and spoken


• Strong analytical, structured, and detail-oriented working style with a high level of independence and reliability


• Confident communication and presentation skills, including the ability to explain complex topics clearly


• Agile mindset with an understanding of modern working methods and the Product Owner role


• Committed, flexible team player with enthusiasm for complex topics and occasional willingness to trave

LOCATION: 

Hybrid with Office in Hannover, Lower Saxony: Regular in-person presence at the office (2 to 3 days per week after the probationary period). Occasional travel to other company locations and clients across Europe is required.

WHAT CAN WE OFFER YOU? 🤩

💰 Competitive Salary (dependent on experience)

🎁 Extensive benefit programme

👥 Company-wide meet-ups

🌍 International work environment with cross-border responsibilities

🌴 Generous annual leave entitlement

 📍 Hybrid environment – a mixture of office and home working

⭐️ Flexible working – to help maintain a better work/life balance

We bring together diverse backgrounds and expertise, and our team is dynamic, solutions-focused, and committed to delivering excellence. If you are a results-driven Medical Writer professional looking for an opportunity to help shape the future of a growing business, we'd love to hear from you!

Last but not least:

• This role is open to full-time applicants only (40h per week).


• No agencies please.


• Unfortunately, we are unable to sponsor candidates for this role.