Clinical Development Manager

Una Health

Clinical Development Manager validating the efficacy of digital therapies for metabolic diseases at Una Health. Leading clinical studies and collaborating with academic and interdisciplinary teams in Berlin.

Posted 7/28/2026full-timeBerlin • 🇩🇪 GermanyMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading and coordinating clinical studies, particularly Randomized Controlled Trials (RCTs) and Real-World Evidence (RWE), while ensuring compliance with regulatory standards. Proficient in analyzing scientific data to support product development and regulatory approvals in the digital health sector.

Highest-signal resume keywords

Clinical Study ManagementRegulatory Compliance (MDR, DiGAV)Data Analysis and InterpretationCRO and Study Center ManagementBusiness-Fluent German and English

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)Regulatory Knowledge (MDR, DiGAV)Good Clinical Practice (GCP)Scientific Data AnalysisBudget NegotiationProject PlanningDigital Health Solutions DevelopmentScientific Publication Preparation

Soft Skills

CollaborationCommunicationLeadershipInterdisciplinary TeamworkNegotiation

Industry Keywords

Digital TherapyMetabolic DiseasesPharmaceuticalMedtechDiGA

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support us in validating the efficacy of our innovative digital therapy
Lead and coordinate clinical studies (RCTs, RWE) to evaluate our digital therapies for metabolic diseases
Work closely with our academic partners, study sites, and external service providers (e.g., CROs) in the execution of studies
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 and regulatory standards

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 in planning and conducting clinical studies (RCTs, RWE) in the pharmaceutical, medtech, or DiGA/digital health environment
Demonstrable strength in selecting and managing CROs and study centers, including negotiating budgets and timelines
Solid knowledge of the regulatory landscape (MDR, DiGAV) and GCP
Business-fluent German and English, both written and spoken

Benefits

Comp & perks

The opportunity to tackle one of the world’s major health challenges
Flexible hybrid work in Berlin
Competitive, experience-based salary
A healthy work–life balance
Flexible working hours
An international team
A network of inspiring colleagues across our networks