What are the responsibilities and job description for the Medical Director, Global Medical Affairs Lead, Diabetes and Metabolism - US, Remote position at Amgen?
HOW MIGHT YOU DEFY IMAGINATION?
If you feel like youre part of something bigger, its because you are. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of.
Medical Director, Global Medical Affairs Lead, Diabetes and Metabolism - US, Remote
Live
What you will do
Lets do this. Lets change the world. In this vital role the Medical Director is the single point of Medical accountability for their allocated product in the relevant indications. The Medical Director drives the development and execution of product Medical strategies to maximize Amgen's value proposition in alignment with product strategies across relevant geographies.
Responsibilities :
Strategy Development and Implementation :
- Contribute to the development and execution of the global medical affairs strategy for Diabetes related products.
- Serve as the Medical Affairs Representative on various global strategic teams.
- Support the development of the integrated evidence generation plan for Diabetes and related conditions.
- Capture clinical / scientific insights across all key markets and translate them into concrete strategies.
- Facilitate scientific engagements across a broad range of partners (e.g. KOLs, Professional Organizations, Payers, Regulators)
- Align and implement strategy for medical communications and related activities.
- Develop medical strategic plans and ensure consistent execution of outputs through Medical Affairs Teams.
- Provide strategic direction for study design and execution for medical affairs and other global studies.
- Enable access to medicines through clear understanding and education of treatment value.
- Facilitate and continue to build Amgens role as a science-based, patient-focused partner.
- Provide input to Value Dossiers.
- Determine resource and budget allocation necessary to deliver on medical strategies.
Evidence Generation and Communication :
Collaboration and Coordination :
Compliance and Performance :
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The ideal candidate we seek is a team player that can adapt easily to a fast-changing environment and possesses the following qualifications :
Basic Qualifications :
Doctorate degree and 4 years experience in a leadership role in clinical research and / or medical affairs
Masters degree and 8 years experience in a leadership role in clinical research and / or medical affairs
Bachelors degree and 10 years experience in a leadership role in clinical research and / or medical affairs
In addition to meeting at least one of the above requirements, you must have at least 4 years experience directly managing people and / or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above
Preferred Qualifications :
MD plus accredited fellowship in Endocrinology, Diabetology, Obesity, Internal Medicine or related medical field. Board-certified or board eligible
PAs, NPs, RDs, PhDs or PharmDs will be considered based on individuals profile
Clinical experience and disease knowledge base in diabetes and metabolic conditions.
MD plus accredited fellowship in Endocrinology, Diabetology, Obesity, Internal Medicine or related medical field. Board-certified or board eligible
3 years of clinical research and / or medical affairs experience in a leadership role
5 years of Medical Affairs experience in industry (biotech, pharmaceutical or CRO)
Experience in building Integrated Evidence Generation Plans
Ability to establish interactions and engagements with partners (e.g., Opinion Leaders, advocacy groups, patients, payers, vendors)
Familiarity with global regulatory organizations, guidelines, and practices
Knowledge of Good Clinical Practices (GCP) and global regulations and guidelines
Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including but not limited to, clinical operations, commercial, regulatory, and medical affairs
History of solving problems while exhibiting sound scientific / medical judgment and a balanced, realistic understanding of issues
Good understanding of healthcare systems around the world (e.g. US, EU, Asia)
Track record of success working with matrixed cross-functional teams
Thrive
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $240,179. to $288,484. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications.
In addition to the base salary, Amgen offers a Total Rewards Plan comprising health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work / life balance, and career development opportunities including :
Apply now
for a career that defies imagination
Objects in your future are closer than they appear. Join us.
careers.amgen.com
Application deadline
Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.
obesity
Salary : $240,179 - $288,484
