Clinical Research Senior Medical Director, Inflammation
US - California - Thousand Oaks - Field/Remote, United States
Career Category
Clinical DevelopmentJob Description
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Clinical Research Senior Medical Director
What you will do
Let’s do this. Let’s change the world. In this vital role you will serve as clinical expert to provide clinical/scientific knowledge into the development, delivery and communication of the global scientific/medical evidence plan for the indication(s). Additional responsibilities include:
- Provide medical leadership for clinical trial(s) and develop and implement strategies to drive patient enrollment in partnership with clinical operations and medical affairs organizations.
- Provide oversight of Patient Impact Expansion (PIE) clinical development with input on global strategy
- Support cross-functional and global collaborations to integrate broad medical, regulatory, safety, scientific, and commercial access and value input into the development program(s)
- Participate and provide clinical input into safety and regulatory interactions.
- Interpret and communicate clinical trial data.
- Author/review CSRs, publications and regulatory submissions
- Develop key opinion leaders and make scientific presentation at advisory boards, key
- scientific meetings and external committee meetings as delegated by GDL
- Identify new clinical research opportunities.
- Support in-licensing and out-licensing activities and partner relationships Support Patient Impact Expansion (PIE) for new indications as directed by Global Development Lead
- Provide clinical content input to materials to be used in Scientific Affairs as well as the Commercial Organization
- Approximate 10% travel may be required.
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a leader with these qualifications.
Basic Qualifications:
MD or DO degree from an accredited medical school
AND
5 years of clinical research and/or basic science research experience
AND
5 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources
Preferred Qualifications:
- MD plus accredited residency in relevant sub-specialty, board certified or equivalent. Five (5) or more years of clinical development experience and/or basic science research combined with clinical teaching and patient care activities.
- Clinical development experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company)
- Experience in development lifecycle management to include development strategy creation for large programs from early development, through late development and commercialization.
- Involved in filing activities as part of the moving the program through the development lifecycle.
- Key relationship development and collaboration with the expansive commercial and medical teams internal and external partners and key opinion leaders.
- Previous management experience of clinical development professionals
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. 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, based on eligibility, comprising of 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 that may include:
- A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
- A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
- Stock-based long-term incentives
- Award-winning time-off plans
- Flexible work models, including remote and hybrid work arrangements, where possible
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
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.
As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
.Salary Range
288,166.00 USD - 362,695.00 USD ApplyJob Profile
Approx. 10% travel Field/Remote Hybrid Partial remote work Remote
Benefits/PerksAnnual bonus program Career development Career development opportunities Collaborative culture Competitive benefits Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Hybrid work Life and Disability insurance Patient impact Personal growth Professional and personal growth Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans
Tasks- Author/review scientific documents
- Collaboration
- Communication
- Contribute to scientific materials
- Develop and implement strategies
- Develop key opinion leaders
- Develop strategies for patient enrollment
- Identify research opportunities
- Interpret and communicate trial data
- Lead clinical trials
- Oversee clinical development
- Present at scientific meetings
- Provide clinical input
- Provide clinical/scientific knowledge
- Support global collaboration
- Support licensing activities
Access Advisory board participation Basic Science Research Biopharmaceutical Biopharmaceutical Industry Biopharmaceutical industry experience BioTech Biotech industry experience Career Development Clinical Development Clinical development strategy Clinical operations Clinical Research Clinical Teaching Clinical trial data Clinical Trial Design Clinical trial oversight Clinical trials Collaboration Commercial Commercialization Communication Cross-functional Collaboration Data analysis Data interpretation Development Development lifecycle management External committee engagement Global Strategy Global Strategy Development Inflammation In-licensing Insurance Key opinion leader development Leadership Lifecycle Management Management Medical Affairs Medical content development Medical Director Medical Education Medical Leadership Medical Writing Oncology Operations Organization Out-licensing Partner relationship management Patient care Patient enrollment strategies People Pharmaceutical Presentation Program Management Project Management Publications Quality Rare Disease Regulatory Interactions Regulatory Submissions Research Resource Allocation Safety Safety and regulatory compliance Safety Monitoring Sales Scientific communication Scientific Knowledge Scientific presentation Scientific publications Strategy Team Leadership Teams Therapeutic Area Expertise Therapeutic Areas
Experience5 years
Education Certifications TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9