3277 2024 copenhagen English-speaking jobs in Capital Region of Denmark

You'll be working in-person in your HQ in Copenhagen where you will constantly be pushed out of your

You'll be working in-person in our HQ in Copenhagen where you will constantly be pushed out of your

You'll be working in-person in our HQ in Copenhagen where you will constantly be pushed out of your

You'll be working out of our HQ in Copenhagen and to ensure a never ending growth curve, we provide

You'll be working in-person in our HQ in Copenhagen where you will constantly be pushed out of your

Sell CPM software and related services in a defined territory. Cross-sell products to existing customers and complete the entire sales cycle.

You'll be working in-person in your HQ in Copenhagen where you will constantly be pushed out of your

You'll be working in-person in your HQ in Copenhagen where you will constantly be pushed out of your

You'll be working out of our HQ in Copenhagen and to ensure a never ending growth curve, we provide

You'll be working in‐person in your HQ in Copenhagen where you will constantly be pushed out of your

You'll be working out of our HQ in Copenhagen and to ensure a never-ending growth curve, we provide

You'll be working out of our HQ in Copenhagen and to ensure a never ending growth curve, we provide

You'll be working out of our HQ in Copenhagen and to ensure a never-ending growth curve, we provide

You'll be working out of our HQ in Copenhagen and to ensure a never ending growth curve, we provide

You'll be working in‐person in your HQ in Copenhagen where you will constantly be pushed out of your

The full-time position is based in Copenhagen and reports to the Chief Legal Officer.

Senior Clinical Research Manager oversees clinical operations, ensuring high-quality study execution in compliance with ICH GCP, SOPs, and protocols. Leads, supports, and provides oversight to CRAs, develops monitoring plans, and manages site activities. Requires a degree in life sciences, minimum 7 years of clinical research experience, and experience with line management or functional oversight of CRAs.

The Senior Clinical Trial Associate coordinates and maintains study documentation, ensuring compliance with ICH GCP, SOPs, and regulatory requirements. Supports study team across all phases, from start-up through close-out. Dedicated to one sponsor, supporting a Phase 2 cardiology study.

Clinical Scientist provides scientific support to clinical development programs, contributing to study design, execution, and data interpretation. Requires advanced scientific degree, clinical research experience, and knowledge of GCP principles. Experience in neuroscience is required.

permanent role with hybrid working location based in Helsinki, Finland, Gdansk / Gdynia / Warsaw, Poland, Copenhagen