Senior – Clinical Research Scientist

About Us

At Chapter 2, we’re not just scaling businesses—we’re reshaping the future of talent acquisition with passion, loyalty, and an unwavering commitment to results. By blending people, processes, and cutting-edge technology, we’ve redefined the traditional RPO model, delivering faster, smarter, and more cost-effective solutions that exceed expectations.

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We are relentless in our pursuit of excellence, embedding world-class talent, pioneering technology, and compelling employer branding into organizations across industries. Our approach isn’t just about recruitment—it’s about building long-term success for our clients.

We are loyal to our clients, to our vision, and most importantly, to each other—because we know that true success is built together.

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(Senior) Clinical Research Scientist – Digital Cardiology & Heart Failure

Location: Berlin

Type of role: Permanent

Sector: Digital Health / Medical Technology (Cardiology & AI)

Working environment: Office-based with flexibility

Breakdown of hybrid arrangement: Hybrid (minimum 3 days in the office) or remote (less preferred)

Working days and hours: Monday to Friday, full time

Language requirements: Fluent in spoken and written English, German is a bonus

Benefits:

• A competitive compensation package with the possibility of receiving company shares

• Macbook         

• Iphone

• Access to the Urban Sports Club so you can stay fit.

• The unique opportunity to positively influence the lives of millions of people.

• A dynamic start-up with an ambitious, interdisciplinary team.

We are supporting an innovative digital health company that is redefining how heart failure is monitored and managed through advanced machine learning technology. Their platform enables clinicians to detect deterioration earlier than traditional methods and improve patient outcomes at scale.

They are now looking for a (Senior) Clinical Research Scientist (MD, PhD, or equivalent) with a strong cardiology background to join their growing medical and scientific team and play a key role in building the clinical evidence behind a next-generation digital cardiology solution.

This is not a back-office research role. You will sit at the centre of the organisation, connecting clinical research, scientific development, and medical affairs in a fast-paced startup environment, with real influence over both scientific direction and clinical impact.

What You’ll Do

Clinical Research & Trial Oversight

• Oversee sponsor-side clinical operations and budgets across multi-centre studies in Europe and the U.S.

• Lead, execute, and monitor clinical trials in collaboration with CROs and internal research teams

• Ensure adherence to GCP and regulatory requirements across all research activities

• Contribute to protocol design, endpoint definition, and data interpretation alongside R&D and data science teams

• Build and maintain strong relationships with investigators, study sites, and clinical partners

• Scientific Development & Dissemination

• Draft and co-author scientific publications and conference presentations for leading cardiology and digital health congresses (ESC, AHA, HFSA, etc.)

• Support preparation of clinical study reports, regulatory submissions, and grant-related deliverables

• Translate clinical data and scientific literature into actionable insights that directly influence product development

Cross-Functional Collaboration

• Work closely with technical R&D teams to validate AI models and translate clinical findings into algorithmic improvements

• Provide clinical and scientific input to commercial and partnership activities as a trusted medical expert

• Ensure clinical context and thinking are embedded across all departments

 What We’re Looking For

Required:

• MD or PhD in Medicine, Biomedical Sciences, or a related field

• Clinical or research experience in cardiology

• At least 2 years’ experience in clinical practice, research, digital health, or medical device development

• Strong understanding of clinical trial methodology and GCP

• Experience authoring and publishing scientific papers

• Excellent communication and writing skills for both clinical and technical audiences

• Based in Berlin with willingness to travel nationally and internationally

Strong Plus:

• Experience in heart failure, remote monitoring, and/or the U.S. healthcare system

• Regulatory experience (ISO 14155, MDR, FDA)

• Proven track record managing multi-centre clinical trials

• Business, strategy, or data analytics experience