Clinical Research Medical Director, Endocrinology/Sleep Apnea, US - Remote
US - California - Thousand Oaks - Field/Remote
Career Category
ClinicalJob Description
HOW MIGHT YOU DEFY IMAGINATION?
At Amgen, every challenge is an opportunity. And every opportunity brings the potential to change lives. Our shared mission—to serve patients—has driven our status as one of the world’s preeminent biotechnology companies, reaching over 10 million patients worldwide. Leverage your high-level expertise to lead and forge partnerships that advance the biotechnical and biopharmaceutical science that can turn the tide of serious, life-interrupting illnesses.
Clinical Research Medical Director, Endocrinology/Sleep Apnea
What you will do
Let’s do this. Let’s change the world. The Obesity organization is seeking a Medical Director that will work with a team of physician-scientists that support evidence generation for obesity and obesity-related conditions with a special focus on sleep disorders.
Responsibilities:
Provide clinical/scientific knowledge into the development, design, delivery, and communication of the global evidence generation plan for multiple metabolic assets.
Support cross-functional and global collaborations to integrate broad medical, scientific, and commercial input into the development program
Participate and provide clinical input into safety and regulatory interactions
Interpret and communicate clinical trial data
Oversee the authoring of clinical study reports, publications, and regulatory submissions
Develop relationships with key opinion leaders and make scientific presentation at advisory boards, key scientific meetings and external committee meetings as delegated by Global Development Lead
Provide clinical content input to materials to be used in Scientific Affairs as well as the Commercial Organization
Contribute to TPP (target product profile) and Global Product Safety (GPS) development
Create development options and present to Global Dev Review Committee (GDRC), Therapeutic Area Governance (TAG)
Interact with TA leadership and extended team to develop strategies options
Interact with Center for Design Analysis (CfDA), Center for Observational Research (CfOR), Clinical Pharmacology Modeling & Simulation (CPMS), etc., to bring innovative later development options.
Win
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The medical professional we seek is a leader with these qualifications.
Basic Qualifications
MD or DO degree from an accredited medical school
AND2 years of clinical research experience and/or basic science research
Preferred Qualifications:
Five (5) years of clinical research experience in the biopharmaceutical industry (biotech, pharmaceutical or CRO company) in obesity or obesity-related conditions with a specific focus on sleep-related disorders like sleep apnea.
Eight (8) years of clinical research experience and/or basic science research combined with clinical teaching and patient care activities
Oversee late phase evidence generation from Phase 2 and beyond by leading the design and implementation of the Total Evidence Generation Plan (EGP), including registrational, non-registrational, and real-world evidence
Previous experience in regulatory interactions and filing activities for Endocrinology/Obesity products
Experience with developing study concepts for clinical development and clinical trial designs with cross functional input, including biostatistics, observational research and patient reported outcomes in Phase 1, 2 and/or 3 clinical trials in obesity or diabetes
Strong and versatile clinical development experience in endocrinology and accreditation in relevant sub-specialty
Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes
Knowledge of Good Clinical Practices (GCP), FDA and EMEA/CHMP regulations and guidelines, and applicable international regulatory requirements
Leadership experience/potential as a medical expert in a complex matrix environment
Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication
Strong interpersonal skills and problem-solving abilities while exhibiting superior judgment and a balanced, realistic understanding of issues and resolution path
They will also embody the Amgen leadership attributes which are:
Inspire: Create a connected, inclusive, and inspiring work environment that empowers talent to thrive
Accelerate: Enable speed that matches the urgency of patient needs by encouraging progress over perfection
Integrate: Connect the dots to amplify the collective power of Amgen to drive results for patients, staff, and shareholders
Adapt: Lead through change by adapting to an ever-changing environment and defining a clear course of action to deliver results
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 $256,334. to $318,868. 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:
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 and bi-annual company-wide shutdowns
Flexible work models, including remote work arrangements, where possible
Amgen’s Commitment to Our Staff
At Amgen, our mission is serving patients. Our staff are dedicated to pushing the boundaries of science to transform medicine and turn the tide on serious illnesses. Central to achieving this mission is our “people-first” philosophy. We recruit the best talent, build an environment that facilitates career growth, and provide staff with the opportunity to make significant contributions for patients and our business.
We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
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.
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.
.Salary Range
256,334.00 USD - 318,868.00 USD ApplyJob Profile
Field/Remote
Benefits/PerksAnnual bonus program Career development Career development opportunities Career growth Comprehensive employee benefits Comprehensive employee benefits package Discretionary annual bonus Financial plans Flexible Spending Accounts Flexible work models Health and welfare plans Life and Disability insurance Personal growth Professional and personal growth Remote work Remote work arrangements Retirement and Savings Plan Stock-based long-term incentives Time-off plans Total Rewards Plan Welfare plans
Tasks- Communication
- Develop relationships
- Develop relationships with key opinion leaders
- Lead evidence generation
- Oversee clinical study reports
- Provide clinical input
- Provide clinical input for regulatory interactions
- Support cross-functional collaborations
Analysis Basic Science Research Biopharmaceutical Biopharmaceutical Industry Biostatistics BioTech Biotechnology Clinical Development Clinical Pharmacology Clinical Research Clinical Study Reports Clinical trial data Clinical Trial Design Clinical trials Commercial Communication Data interpretation Development Diabetes Endocrinology Evidence Generation FDA GCP Good clinical practices Governance Insurance International regulatory requirements Interpersonal Key Opinion Leader Engagement Leadership Leadership Attributes Matrix Environment Metabolic Modeling Obesity Observational Research Oral communication Organization Patient care Patient reported outcomes People Pharmaceutical Pharmaceutical Product Development Pharmacology Presentation Problem-solving Product Development Product Lifecycle Publications Real-World Evidence Regulatory Interactions Regulatory Submissions Research Safety Sales Scientific communication Scientific Knowledge Simulation Sleep disorders
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