Regulatory Submissions Jobs in Germany

About Charles River AssociatesCharles River Associates is a leading global consulting firm that provides economic financial and business management expertise to major law firms corporations and governments around the world. CRA advises clients on economic and financial matters pertaining to litigati...

About Charles River AssociatesCharles River Associates is a leading global consulting firm that offers economic financial and strategic expertise to major law firms corporations and governments around the world. Since 1965 CRA experts have combined rigorous cutting-edge research state-of-the-art met...

JoinIQVIA as Trainee Clinical Research Associate / Associate CRA (m/w/d) in the sponsor dedicated team and work in home-office throughout Germany. In our Clinical Functional Service Partnership models we work in a close partnership with key customers to deliver a comprehensive clinical trial managem...

About usAt Ada we envision a world where everyone gets the healthcare they need. Yet millions remain undiagnosed and untreated due to the complexity of identifying rare and underrecognized conditions even when effective treatments exist.Were changing that. Powered by leading AI and built by a team o...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

ABOUT THE COMPANYAt inne we have seen firsthand how womens need for female health education and accurate fertility insights have been underserved. So we made it our obsession to use the best of science tech and design to bring actionable scientific insights into female health.We are an interdiscipl...

Define and lead the global Clinical Affairs strategy for Brainlabs global surgery portfolio ensuring alignment with product regulatory and commercial objectives / teamsLead and develop an international Clinical Affairs team responsible for clinical evaluation clinical research and scientific marketi...

Job DescriptionFür unseren Standort Köln suchen wir ab sofort unbefristet und in Vollzeit eine starke QA-Persönlichkeit (m/w/d) die Qualität nicht nur absichert sondern im Alltag wirksam macht.Als Quality Assurance Lead übernimmst du die unabhängige QA-Oversight für alle GMP-relevanten Aktivitäten a...

Title: CMC Regulatory ConsultantLocation: Munich Germany (12 days remote working)Position: Permanent opportunityRate: Competitive market salary CK Group are recruiting on behalf of a science-led pharmaceutical and biotechnology consultancy providing expert CMC quality and regulatory support across d...

The job that makes possibilities real in patients lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48000 employees worldwide and around 3000 employees in Germany you will have the opportunity of addressin...

The job that makes possibilities real in patients lives. And yours.The job that helps you get ahead in life. Moving mountains together.Welcome to AbbVie! As part of an international company with 48000 employees worldwide and around 3000 employees in Germany you will have the opportunity of addressin...

Join IQVIA as a Clinical Research Associate 2 / CRA II and work home-based in Southern Germany or in the Frankfurt area in our single sponsor department.You will enjoy the stability and resources of a leading global contract research organization while gaining direct experience with one of our clien...

Are you passionate about advancing healthcare through cuttingedge medical technologyJoin IQVIA MedTech as a Clinical Research Associate 2 / CRA 2 (m/w/d) in home-office throughout Germany and help shape the future of patient care.In this role youll work with innovative medical devices that push the...

The central Legal & Compliance team at Miele currently consists of 26 dedicated employees and acts as a reliable business partner for all operational units central functions international locations and management in all legal matters. To strengthen international cooperation with in-house legal colle...

Define and lead the global Clinical Affairs strategy for Brainlabs global surgery portfolio ensuring alignment with product regulatory and commercial objectives / teamsLead and develop an international Clinical Affairs team responsible for clinical evaluation clinical research and scientific marketi...

Your daily workoutWould you like to revolutionise the fitness and health industry with us and make your contribution to a healthier society We are looking for a Product Compliance Manager (m/f/d) who wants to join us in our mission we make the gym work for everyone! and to actively shape the future...

About the opportunityThe Senior Reporting Data Analyst plays a key role in supporting the French Regulatory Reporting team by developing maintaining and optimizing the data models pipelines and scripts used for French regulatory submissions. The role ensures high-quality data reliable transformation...

Shape the future of regulatory excellence at IQVIAAt IQVIA we work to advance healthcare by helping our clients bring safe effective medicines to patients. As a Regulatory Affairs Specialist you will play a key role in ensuring compliance and supporting successful product lifecycle management across...

Shape the future of regulatory excellence at IQVIAAt IQVIA we work to advance healthcare by helping our clients bring safe effective medicines to patients. As a Regulatory Affairs Specialist you will play a key role in ensuring compliance and supporting successful product lifecycle management across...

Work Flexibility: Remote or Hybrid or OnsiteGrow Your Career at Stryker as an Associate Manager Clinical Data Science!As an Associate Manager for Clinical Data Sciences you will lead a diverse team of experts and collaborate with internal and external stakeholders to implement and execute Clinical D...