✨ The Role in One Sentence

Join COLDPLASMATECH as a Medical Affairs Manager to drive clinical studies, optimize processes, and support regulatory affairs in wound therapy innovation.

📋 What You'll Likely Do

• 30%: Support clinical studies and projects, ensuring alignment with company goals.

• 25%: Analyze clinical data and create scientific publications to advance wound care knowledge.

• 25%: Assist in regulatory affairs for medical device commercialization and clinical evaluation.

🧑‍💻 Profiles Doing This Job

• High Priority: Completed scientific studies in medicine, medical technology, biology, or pharmacy.

• High Priority: 5+ years in Medical Affairs or Clinical Research in the medical device industry.

• High Priority: Strong knowledge of regulatory requirements for clinical studies and medical device evaluations.

📈 How This Role Will Look on Your CV

• Managed clinical studies and regulatory processes in a MedTech company focused on innovative wound therapies.