Clinical Project Manager

Upsilon Global, a renowned leader in the healthcare industry, is currently looking for a skilled Freelance Project Manager to oversee a Cardiology Device Study based in Austria. Our company is dedicated to advancing medical research and improving patient outcomes through innovative clinical studies. We foster a collaborative work culture that values excellence, integrity, and teamwork.

As the Project Manager for this exciting opportunity, you will be responsible for managing all aspects of the Cardiology Device Study in Austria. Your key duties will include overseeing study timelines, ensuring regulatory compliance, and facilitating effective communication with stakeholders. You will play a vital role in leading and coordinating the clinical study to ensure successful outcomes within specified timelines and budgets.

The ideal candidate for this role should possess at least 5 years of clinical trial project management experience, with a strong background in cardiology medical device studies being highly advantageous. Knowledge of Austrian and EU clinical trial regulations is essential for this position. Additionally, strong leadership skills, excellent communication abilities, and problem-solving capabilities are crucial for success in this role. Fluency in English is required, while proficiency in German would be considered a valuable asset.

If you are passionate about making a difference in the field of cardiology research and have the necessary experience and skills to excel as a Clinical Project Manager, we encourage you to apply for this position. This role is suitable for mid-career professionals seeking to take on challenging responsibilities within an esteemed organization like Upsilon Global. Join us in our mission to drive innovation and improve patient care through cutting-edge medical research projects. Contact Amani Manaka or call +44 203 875 9966 for more details on how you can become part of our dynamic team!

• 5+ years of clinical trial project management experience
• Experience in cardiology medical device studies
• Knowledge of Austrian and EU clinical trial regulations
• Strong leadership, communication, and problem-solving skills

• Lead and coordinate the clinical study, ensuring adherence to timelines and budgets
• Manage regulatory submissions, ethics committee approvals, and site activation
• Oversee risk assessment, mitigation strategies, and troubleshooting
• Collaborate with internal teams, sponsors, and regulatory authorities

• Clinical trial project management
• Cardiology medical device studies
• Regulatory compliance
• Stakeholder communication
• Leadership

Seniority Level: Senior Level

Job Functions: Project Management

• Clinical Research
• Regulatory Compliance

Industries : Healthcare

• Medical Devices
• Clinical Trials