Lead Medical Specialist in Rare Blood Disorders
4 weeks ago
About the Role
We are seeking a highly skilled Lead Medical Specialist to join our team at Novo Nordisk A/S. As a key member of our Medical & Science, Rare Blood Disorders department, you will play a vital role in driving clinical development strategies and programs for our rare disease portfolio.
Job Description
As a Lead Medical Specialist, you will be responsible for designing and implementing clinical trials, providing medical oversight, interpreting trial results, and supporting submissions to health authorities. You will also have a key role as an author for publications of clinical trial data and engage with scientific experts and health authorities to achieve the best possible clinical development programs.
You will work closely with cross-functional teams and colleagues globally, requiring strong communication skills and the ability to collaborate effectively. Travel activities are estimated to be approximately 15-20 days per year.
Qualifications and Requirements
- A Medical Doctor degree, preferably with a PhD, and experience in hematology/pediatrics/hemoglobinopathies is an advantage.
- At least 3 years of clinical drug development experience from the pharmaceutical industry, with the capability of providing mentorship and training to junior colleagues.
- Excellent stakeholder management skills and proficiency in English.
What We Offer
We offer a competitive salary, estimated to be around $120,000 - $180,000 per annum, depending on location and experience. In addition, we provide a comprehensive benefits package, including opportunities for professional growth and development, a collaborative and dynamic work environment, and a chance to make a meaningful impact in the field of rare diseases.
About Us
Novo Nordisk A/S is a global healthcare company committed to making a difference in the lives of patients. Our Medical & Science, Rare Blood Disorders department is part of our larger Clinical Drug Development organization and works closely with internal stakeholders and external partners to develop innovative treatments for rare blood disorders.
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