Medical Writer (m/w/d)

MAP Patient Access; Hannover; Hybrid; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading healthcare consultancy in Hannover is seeking a Medical Writer to support AMNOG and JCA dossier submissions. This role involves scientific analysis, strategic planning, and collaboration with interdisciplinary teams. The ideal candidate has a doctoral degree in a relevant field, fluency in both German and English, and experience in writing scientific texts. The position offers a competitive salary and a hybrid work model, with regular office presence after the probationary period.

Leistungen

Competitive salary

Extensive benefit programme

Generous annual leave

Flexible working

Company-wide meet-ups

Qualifikationen

• Ideally initial professional experience in consulting market access or related field.
• Knowledge of the German healthcare system and pharmaceutical market.
• Experience in interpreting and presenting scientific data.

Aufgaben

• Contribute to AMNOG and JCA dossier strategy and submission.
• Prepare submissions and participate in strategic projects.
• Assist in developing templates and best practices.

Kenntnisse

Native-level proficiency in German

Native-level proficiency in English

Scientific writing

Analytical thinking

Project management

Multilingual communication

Ausbildung

Doctoral degree in Natural Sciences

Pharmacy

Medicine

Tools

MS-Office

data tools

LaTeX

Jobbeschreibung

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.

Our clients in healthcare and life sciences are leading innovators in pharma, biotech, medtech, digital health, and diagnostics. As part of Kintiga, we support the successful launch and reimbursement of breakthrough therapies and technologies.

Join our team and help shape the future of the cutting‑edge healthcare solutions. At Kintiga, we cultivate a collaborative and entrepreneurial culture where every voice matters. We value diversity, openness, and integrity - encouraging our team members to bring their ideas and passion to work every day. Become part of a supportive, dynamic team that thrives on innovation, lifelong learning, and making a meaningful impact in healthcare and life sciences.

WHAT WE'RE LOOKING FOR 🔍

As a Medical Writer, you will play a key role in supporting the preparation and submission of AMNOG and JCA dossiers while contributing to G‑BA consultations and Joint Scientific Consultations (JSCs). In this position, you will provide scientific expertise and assist with strategic planning to ensure high‑quality deliverables.

Your responsibilities include contributing to dossier strategies and writing the dossier modules, preparing submissions using tools such as our proprietary EPRI, and actively participating in strategic projects, risk assessments, and price negotiations. Additionally, you will share insights and best practices across teams and support the development of templates, internal tools, and processes to enhance efficiency and quality.

KEY RESPONSIBILITIES ARE:

• Execution of consulting projects with a focus on developing market access and dossier strategies, including preparation of corresponding workshops, and participation in oral hearings with relevant authorities.
• Independent preparation of benefit assessment dossiers for pharmaceuticals within the framework of the AMNOG process (for further information: benefit assessment of pharmaceuticals) as well as EU Health Technology Assessments (HTA) in collaboration with our clients.
• Scientific and statistical analysis, interpretation, gap analysis, and presentation of clinical study results.
• Independent review of scientific literature and preparation and documentation of qualitative and quantitative analyses.
• Collaboration in interdisciplinary, agile teams composed of clients and colleagues.
• Application of state‑of‑the‑art, AI‑supported technological solutions and New Work methods (e.g., Design Thinking, SCRUM, Kanban).
• Active contribution to the continuous development of Kintiga.
• Targeted training and professional development in key market access disciplines.

DETAILED RESPONSIBILITIES ARE:

Primary Focus

• Contributing AMNOG and JCA dossier strategy, preparation (including use of EPRI), and submission.
• Supporting G‑BA consultations and Joint Scientific Consultation (JCA).

Cross‑functional Involvement

• Participating in strategic projects, risk assessments, and price negotiations.

Knowledge Contribution

• Assisting in the development of templates, best practices, and internal tools.

Core Consulting Skills

• Manage deliverables for defined project modules and ensure quality and timelines.
• Apply structured problem‑solving independently and generate actionable insights.
• Present own results confidently to internal teams and clients in German & English.
• Contribute to client‑facing work and support business development and marketing activities.

Agile Working

• Apply and further develop agile working methods in project contexts.

Strategic & Business Acumen

• Build expertise in specific domains (e.g., HTA, pricing) and apply it to diverse project contexts.

Business Development

• Take ownership of specific proposal sections and support opportunity identification.

Corporate Development

• Participate in competence teams and contribute to method development.

Cultural Ambassador

• Act as a cultural ambassador by living and promoting company values.
• Foster collaboration, transparency, and trust within teams and across functions.
• Contribute to a positive and inclusive team culture through active engagement and role modeling.

ABOUT YOU 🚀

• Doctoral degree in Natural Sciences, Pharmacy, Medicine, or a closely related field.
• Ideally initial professional experience in consulting market access, medicine or related field.
• Native‑level proficiency in German & English and extensive experience in writing scientific texts and communicating in both languages.
• Knowledge of the German healthcare system, the pharmaceutical market, and the relevant legal framework.
• Experience in interpreting and presenting scientific and clinical data, as well as conducting literature research.
• Advanced skills in MS‑Office CRM, project management, and data tools (preferred), knowledge of LaTeX is an advantage.
• Strategic & structured mindset, analytical thinking, numerical understanding and problem‑solving ability.
• Reliability and a meticulous & client‑oriented approach with a strong commitment to delivering high‑quality results.
• Excellent organizational, agile and classic project management skills.
• Self‑motivated, proactive and able to work independently and as part of a team.
• Occasional availability to travel.
• Multilingual communication skills (preferred).

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.

⭐️ Flexibleworking – 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.