Clinical Affairs Director

vor 3 Wochen


Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

{"h3": "Your Mission

As a Clinical Affairs Manager at POLYTECH Health & Aesthetics GmbH, you will play a crucial role in ensuring the compliance of our medical devices with international regulatory standards. Your responsibilities will include leading the development and management of clinical study protocols, overseeing clinical evaluations and post-market surveillance activities, and preparing and submitting clinical papers and documentation to support product registrations and regulatory submissions.", "ul": [{"li": "Develop and implement clinical study protocols that meet international regulatory standards"}, {"li": "Collaborate with cross-functional teams to ensure compliance with regulatory requirements"}, {"li": "Prepare and submit clinical papers and documentation to support product registrations and regulatory submissions"}, {"li": "Monitor and manage ongoing clinical trials to ensure compliance with regulatory requirements and adherence to study protocols"}, {"li": "Conduct risk analysis and provide expert recommendations on clinical safety issues for both new and existing products"}, {"li": "Train and collaborate with internal teams on the latest clinical insights and regulatory standards"}], "h3": "Your Profile

To succeed in this role, you will need to have a strong background in life sciences, healthcare, or a related field, with several years of experience in clinical affairs within the medical device industry. You will also need to have excellent organizational and project management skills, with the ability to work cross-functionally in a dynamic environment. Additionally, you will need to have outstanding communication skills, with fluency in English (both written and verbal), and a high attention to detail with excellent analytical and problem-solving skills.", "ul": [{"li": "Master's degree or PhD in life sciences, healthcare, or a related field"}, {"li": "Several years of experience in clinical affairs within the medical device industry"}, {"li": "Strong knowledge of international regulatory requirements and proven experience in clinical trial management"}, {"li": "Excellent organizational and project management skills"}, {"li": "Hands-on style and can-do mentality"}, {"li": "Outstanding communication skills with fluency in English"}, {"li": "High attention to detail with excellent analytical and problem-solving skills"}, {"li": "Collaborative mindset with the ability to work well in teams"}, {"li": "Located in Germany or Israel"}, {"li": "Willingness for occasional travel"}], "h3": "Why Us?

At POLYTECH Health & Aesthetics GmbH, we offer a diverse and challenging role within a leading, growth-oriented company at the forefront of the medical field. Our company culture is collaborative and respectful, with flat hierarchies and short decision-making paths. We also offer long-term, secure career prospects in an innovative and forward-thinking industry, as well as company-sponsored occupational pension schemes and access to corporate benefits.", "ul": [{"li": "Diverse and challenging role within a leading company"}, {"li": "Collaborative and respectful working environment"}, {"li": "Long-term, secure career prospects"}, {"li": "Company-sponsored occupational pension schemes"}, {"li": "Access to corporate benefits"}, {"li": "Flexible working hours and remote working options"}, {"li": "Comprehensive onboarding and continuous opportunities for personal and professional development"}], "h3": "Contact Details

If you are interested in this role, please contact our HR department for more information.", "p": "We look forward to hearing from you"}



  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    About the RoleWe are seeking a highly skilled Clinical Affairs Manager to lead the development and management of clinical study protocols, ensuring full compliance with international regulatory standards.The ideal candidate will have a strong knowledge of international regulatory requirements and proven experience in clinical trial management.Key...


  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    Your MissionWe are seeking a highly skilled Clinical Affairs Manager to lead the development and management of clinical study protocols, ensuring full compliance with international regulatory standards.This role involves overseeing clinical evaluations and post-market surveillance activities, preparing and submitting clinical papers and documentation to...


  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    Your MissionWe are seeking a highly skilled Clinical Affairs Manager to lead the development and management of clinical study protocols, ensuring full compliance with international regulatory standards.This role involves overseeing clinical evaluations and post-market surveillance activities, preparing and submitting clinical papers and documentation to...


  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    Key ResponsibilitiesAs a Clinical Affairs Manager at POLYTECH Health & Aesthetics GmbH, you will be responsible for leading the development and management of clinical study protocols, ensuring full compliance with international regulatory standards. This includes overseeing clinical evaluations and post-market surveillance activities, preparing and...


  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    Key ResponsibilitiesAs a Clinical Affairs Manager at POLYTECH Health & Aesthetics GmbH, you will be responsible for leading the development and management of clinical study protocols, ensuring full compliance with international regulatory standards.About the RoleYou will oversee clinical evaluations and post-market surveillance activities, preparing and...


  • Dieburg, Hessen, Deutschland POLYTECH Health & Aesthetics GmbH Vollzeit

    Key ResponsibilitiesAs a Clinical Affairs Manager at POLYTECH Health & Aesthetics GmbH, you will be responsible for leading the development and management of clinical study protocols, ensuring full compliance with international regulatory standards. This includes overseeing clinical evaluations and post-market surveillance activities, preparing and...