The Senior Director, Medical Affairs EU is a strategic field-based medical leader responsible for ... Lead development and execution of the European Medical Affairs strategy aligned with global ...
The Senior Director, Medical Affairs EU is a strategic field-based medical leader responsible for ... Lead development and execution of the European Medical Affairs strategy aligned with global ...
Direct all phases of highly technical quality assurance audit activities. * Oversee the Quality ... Knowledge of the European Medical Device Regulation 2017/745. * Knowledge of US FDA Quality ...
Direct all phases of highly technical quality assurance audit activities. * Oversee the Quality ... Knowledge of the European Medical Device Regulation 2017/745. * Knowledge of US FDA Quality ...
The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Client has also entered license agreement negotiations ...
The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Client has also entered license agreement negotiations ...
The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Client has also entered license agreement negotiations ...
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The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Client has also entered license agreement negotiations ...
Direct all phases of highly technical quality assurance audit activities. * Oversee the Quality ... Knowledge of the European Medical Device Regulation 2017/745. * Knowledge of US FDA Quality ...
Direct all phases of highly technical quality assurance audit activities. * Oversee the Quality ... Knowledge of the European Medical Device Regulation 2017/745. * Knowledge of US FDA Quality ...
The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Clienthas also entered license agreement negotiations with ...
The Medical Director / Sr Medical Director will play a key role at all stages of clinical ... The European Launch is in the works. Our Clienthas also entered license agreement negotiations with ...
With global headquarters in Research Triangle Park, North Carolina, and European headquarters in ... Position Summary The Medical Director, Movement Disorders Specialist, GDNF Program will provide ...
With global headquarters in Research Triangle Park, North Carolina, and European headquarters in ... Position Summary The Medical Director, Movement Disorders Specialist, GDNF Program will provide ...
Medical Director, Autoimmunity
San Diego, CA · On-site +1
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Medical Director, Autoimmunity
San Diego, CA · On-site +1
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Medical Director, Autoimmunity
San Diego, CA · On-site +1
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Quick apply
Medical Director, Autoimmunity
San Diego, CA · On-site +1
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Medical Director, Autoimmunity
San Diego, CA · On-site
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Medical Director, Autoimmunity
San Diego, CA · On-site
$290K - $310K/yr
S. and European Health Authority interactions and submission of clinical regulatory documents is desirable. * Willingness to engage with investigators, key opinion leaders, and external advisors, as ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Executive Medical Director, Medical Strategy (hepatologist), is a key member of the Medical ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Executive Medical Director, Medical Strategy (hepatologist), is a key member of the Medical ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Executive Medical Director, Medical Strategy (hepatologist), is a key member of the Medical ...
Rezdiffra is the first and only medication approved by both the FDA and European Commission for the ... The Executive Medical Director, Medical Strategy (hepatologist), is a key member of the Medical ...
The Senior Medical Director will also provide medical safety subject matter expertise in the review ... European Summary of Product Characteristics (SmPC), Canadian Product Monograph (PM), and Risk ...
The Senior Medical Director will also provide medical safety subject matter expertise in the review ... European Summary of Product Characteristics (SmPC), Canadian Product Monograph (PM), and Risk ...
The initial focus will be overall execution and implementation of the European Medical Device ... Direct: (732)-429-1649 Tel: (732) 549 2030 x 230 Fax: (732) 549 5549
The initial focus will be overall execution and implementation of the European Medical Device ... Direct: (732)-429-1649 Tel: (732) 549 2030 x 230 Fax: (732) 549 5549
S. and European medical device regulations, and intimate knowledge of regulations regarding ... 621I DIRECT # - 732 - 318 -6506 | (W) # 732-549-2030 - Ext - 324 | (F) 732-549-5549 Email id ...
S. and European medical device regulations, and intimate knowledge of regulations regarding ... 621I DIRECT # - 732 - 318 -6506 | (W) # 732-549-2030 - Ext - 324 | (F) 732-549-5549 Email id ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
Director, Medical Affairs
Foster City, CA · On-site
Reporting to the Sr. Director of Hepatitis B and C, Global Medical Affairs, this role is a key ... Contributes to the development of European and global medical POAs * Collaborates effectively and ...
The Director Regulatory Affairs, Device is responsible for combining knowledge of scientific ... European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards ...
The Director Regulatory Affairs, Device is responsible for combining knowledge of scientific ... European Medical Device Directives and Regulation (MDR/IVDR), ISO 13485, MDSAP, technical standards ...
... introduction of the European Medical Agency (EMA) introduction of underlying infrastructure ... Direct: 732-662-7964 | (W) 732-549-2030 x 219 Inc. 5000 - 2007-2015 (9 Years in a row)
... introduction of the European Medical Agency (EMA) introduction of underlying infrastructure ... Direct: 732-662-7964 | (W) 732-549-2030 x 219 Inc. 5000 - 2007-2015 (9 Years in a row)
European Medical Director information
See salary details
$13K - $44.3K
2% of jobs
$44.3K - $75.5K
1% of jobs
$75.5K - $106.8K
5% of jobs
$106.8K - $138.1K
3% of jobs
$138.1K - $169.4K
5% of jobs
$197.7K is the 25th percentile. Wages below this are outliers.
$169.4K - $200.6K
9% of jobs
$200.6K - $231.9K
19% of jobs
The median wage is $238.9K / yr.
$231.9K - $263.2K
22% of jobs
$278.3K is the 75th percentile. Wages above this are outliers.
$263.2K - $294.5K
17% of jobs
$294.5K - $325.7K
10% of jobs
$325.7K - $357K
6% of jobs
$13K
$232.4K
$357K
How much do european medical director jobs pay per year?
What does a European Medical Director do?
What is the difference between European Medical Director vs European Medical Advisor?
| Aspect | European Medical Director | European Medical Advisor |
|---|---|---|
| Credentials | Medical degree, often with leadership experience | Medical degree, often with specialized knowledge |
| Work Environment | Strategic leadership, overseeing medical teams and projects | Providing medical expertise, supporting clinical trials and product development |
| Employer & Industry Usage | Pharmaceutical companies, biotech firms, healthcare organizations | Pharmaceutical companies, medical communications, clinical research |
The European Medical Director typically holds a leadership role with strategic responsibilities, overseeing medical teams and ensuring compliance across projects. In contrast, the European Medical Advisor focuses on providing expert medical input to support clinical and product development activities. Both roles require medical credentials, but their scope and focus differ significantly.
How does a European Medical Director typically collaborate with cross-functional teams across different countries?
What are the key skills and qualifications needed to thrive as a European Medical Director, and why are they important?

Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 20 days ago
Job description
Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary arterial hypertension (PAH). We will continue to combine our proprietary, innovative PRINT Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry's top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.
Job Summary:
The Senior Director, Medical Affairs EU is a strategic field-based medical leader responsible for advancing Liquidia's scientific and medical objectives across Europe in pulmonary hypertension and related cardiopulmonary diseases.
This role will lead regional scientific engagement, support evidence-generation initiatives, cultivate strategic relationships with key opinion leaders (KOLs), investigators, and patient advocacy organizations, and partner cross-functionally to support the successful execution of clinical development and future commercialization activities throughout Europe.
The successful candidate will possess deep therapeutic expertise in PAH and PH-ILD, strong clinical research and external engagement experience, and a demonstrated ability to influence scientific strategy within a complex matrix environment. This individual will serve as a critical scientific ambassador for Liquidia across the European pulmonary vascular community.
Job Requirements
- Advanced scientific degree (PharmD, PhD, MD) required.
- More than 15 years of Medical Affairs experience in biotech or pharmaceutical industries, including significant field-based experience as an MSL.
- Strong therapeutic expertise in PAH, PH-ILD, pulmonary hypertension, interstitial lung disease, or related cardiopulmonary conditions preferred.
- Deep understanding of clinical research processes, including best practices and support models for investigator-initiated research (IIR).
- Excellent communication, interpersonal, and coaching skills with a demonstrated ability to motivate and develop field personnel.
- Highly organized, with strong analytical ability and comfort working in a fast-paced, cross-functional environment.
- Ability to travel 60% across Europe.
Job Responsibilities
Strategic Medical Affairs Leadership
- Lead development and execution of the European Medical Affairs strategy aligned with global objectives and regional unmet medical needs in PAH and PH-ILD.
- Establish Liquidia as a scientific leader within the European pulmonary vascular community through high-impact scientific exchange and strategic external engagement.
- Develop regional and national KOL engagement plans targeting pulmonary hypertension centers of excellence, multidisciplinary care teams, investigators, and scientific societies.
- Support EU launch readiness activities, including L606 scientific platform development, stakeholder mapping, advisory engagement, and medical education initiatives.
- Maintain and develop materials related to advanced knowledge of emerging science, treatment paradigms, competitive intelligence, and evolving clinical practice within pulmonary vascular disease.
- Build and maintain strong scientific relationships with KOLs, investigators, site networks, and patient advocacy groups across Europe.
- Represent Medical Affairs at international, national, and regional scientific congresses and ensure coordinated scientific engagement and effective post-congress follow-up activities.
- Identify opportunities to influence scientific dialogue, evidence-generation priorities, and treatment paradigms in PAH and PH-ILD.
- Support scientific exchange related to clinical development programs, unmet medical needs, and real-world treatment challenges.
Job Benefits
Liquidia offers a competitive compensation package as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, Unlimited Paid Time Off and more!
Liquidia is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform the essential functions of this position.
Recruiting Agencies, Please Note :
Liquidia will not accept unsolicited assistance from recruiting/search agencies for this employment opportunity. Please, no phone calls or emails. All resumes submitted by recruiting or search agencies to any employee at Liquidia via email, the Internet or in any form and/or method without a valid written search/recruitment agreement in place for this position will be deemed the sole property of Liquidia. No fee will be paid in the event the candidate is hired by Liquidia as a result of the referral or through other means.
About Liquidia
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
Morrisville, NC, US
Year founded
2004