Clinical Development Manager

Una Health

Clinical Development Manager bei Berliner Digital-Health-Startup für metabolische Gesundheit. Leitung klinischer Studien und wissenschaftlicher Evidenzentwicklung für digitale Diabetes-Therapien.

Posted 8/12/2026full-timeBerlin • 🇩🇪 GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading clinical studies, particularly Randomized Controlled Trials (RCTs) and Real-World Evidence (RWE), while ensuring compliance with regulatory standards. Proficient in collaborating with interdisciplinary teams and external partners to advance digital health solutions for metabolic diseases.

Highest-signal resume keywords

Clinical Study ManagementRegulatory Compliance (MDR, DiGAV)CRO and Study Site ManagementFluent in German and EnglishDigital Health Motivation

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchRandomized Controlled Trials (RCTs)Real-World Evidence (RWE)Data AnalysisRegulatory Knowledge (GCP)Scientific Publication PreparationBudget NegotiationProject PlanningEvidence DevelopmentDigital Therapy Expertise

Soft Skills

Organizational SkillsProactive AttitudeIndependent WorkCommunication SkillsEmpathy

Industry Keywords

Metabolic DiseasesDigital HealthPharmaMedtechDiGAHealthcare ProfessionalsInterdisciplinary CollaborationStakeholder CoordinationScientific Data InterpretationLegal Obligations

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and coordinate clinical studies (RCTs, RWE) investigating digital therapies for metabolic diseases
Work closely with academic partners, study sites and external service providers, e.g., CROs, during study execution
Collaborate internally with interdisciplinary teams to develop innovative digital health solutions
Analyze and interpret scientific data to support regulatory approvals, product development, and communication with healthcare professionals
Support the preparation of scientific publications and presentations
Monitor regulatory requirements and ensure all projects comply with legal obligations
Further develop the evidence base for the digital therapy to sustainably improve care and prevention of metabolic diseases

Requirements

What you’ll need

Degree in medicine, biology, health sciences, pharmacy or a comparable field, or a specific qualification in clinical research
At least 3–5 years of experience planning and conducting clinical studies (RCTs, RWE) in the pharma, medtech, or DiGA environment
Proven ability in selecting and managing CROs and study sites, including negotiating budgets and timelines
Solid knowledge of the regulatory environment (MDR, DiGAV) and GCP
Fluent German and English, both written and spoken
Willingness to work in Berlin
Organized, proactive, and able to work independently
Communicative and empathetic coordination of diverse stakeholders
Motivation for digital health as well as diabetes and metabolic diseases

Benefits

Comp & perks

The opportunity to tackle one of the world’s biggest health problems
Flexible hybrid work in Berlin
Experience-based salary and equity in the company
Diverse development opportunities and flexible working hours
An international team
A network of inspiring colleagues within our networks