Executive Medical Director Early Dev Inflammation - Thousand Oaks CA
Company: Msccn
Location: Thousand Oaks
Posted on: April 1, 2026
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Job Description:
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization
works with partner companies to source qualified talent for their
open roles. The following position is available to Veterans,
Transitioning Military, National Guard and Reserve Members,
Military Spouses, Wounded Warriors, and their Caregivers . If you
have the required skill set, education requirements, and
experience, please click the submit button and follow the next
steps. Unless specifically stated otherwise, this role is "On-Site"
at the location detailed in the job post. What you will do Amgen is
advancing a broad/deep pipeline of Inflammation programs spanning
multiple modalities. We need collaborative and innovative
world-class talent to ensure these molecules become medicines and
reach their full potential while helping patients. Let’s do this.
Let’s change the world. In this vital role the Executive Medical
Director you will serve as an Early Development Inflammation
Portfolio lead for key assets in the Amgen portfolio. You will
serve as the principal representative for an early development
portfolio to a range of audiences, including executive leadership,
development partners, and global regulatory agencies. You will
develop and translate Inflammation development program strategies
into the design and implementation of clinical studies that can be
executed without compromising scientific rigor. The Executive
Medical Director will report into the Associate Vice President,
Early Development. Responsibilities Develop an Early Development
Inflammation team in collaboration with the Early Development
Therapeutic Area Head Ensure the best way to develop and prosecute
an early development portfolio Drive the timely execution of
multiple assets and studies within the early development portfolio
Ensure strategy and execution, and partner closely with Research,
Translational Safety (toxicology), Precision Medicine, Clinical
Pharmacology, Biostatistics, and Clinical Operations colleagues
Partner closely with Regulatory leaders to support regulatory
interactions and develop regulatory strategies Keep major
stakeholders and other senior management updated as the portfolio
evolves and matures Guide their team to think broadly as they
create innovative portfolio development strategy options. Ensure
all avenues and options have been explored and evaluated before
final recommendations are sent for review by senior leadership
Oversee activities related to planning for studies including
execution and oversight of study outlines and Protocols for early
development clinical studies Collaborate with Business Development
colleagues in the evaluation of external opportunities. Mentor,
coach, and supervise the performance of direct reports to build a
highly skilled, diverse, and inclusive team, leading and motivating
staff in a complex, multi-functional matrix environment Additional
Qualifications/Responsibilities What we expect of you We are all
different, yet we all use our unique contributions to serve
patients. The candidate we seek is an experienced leader with the
following qualifications. Basic Qualifications: MD or DO from an
accredited medical school AND Five (5) years of industry or
academic research AND Six (6) years of managerial experience
directly managing people and/or leadership experience leading
teams, projects, programs or directing the allocation of resources
Preferred Qualifications: MD or MD/PhD plus accredited residency in
relevant sub-specialty, board certified or equivalent Relevant
subspecialty board eligibility/certification or equivalent Clinical
research experience in the biopharmaceutical industry (biotech,
pharmaceutical or CRO company) Eight (8) or more years of clinical
research experience and/or basic science research combined with
clinical teaching and patient care activities Proven success record
in how to conceptualize, design, conduct, and analyze early
development clinical trials Ability to anticipate problems and find
creative solutions In-depth understanding of the scientific method
and clinical applications based on medical, scientific and
practical rationale including working knowledge of biomarker
methods and clinical imaging endpoints A record of high-quality
peer-reviewed publications Experience functioning as a medical
expert in a complex matrixed environment Previous experience in
conducting translational and/or clinical research for both small
molecules and large molecules History of solving problems while
exhibiting judgment and a balanced, realistic understanding of
issues including the ability to anticipate problems and find
creative solutions Knowledge of Good Clinical Practices (GCP), FDA
regulations and guidelines, and applicable international regulatory
requirements Knowledgeable in current and possible future, trends,
technology, policies, practices and information of the competitive
landscape of oncology development and global health authority
requirements for oncology drug approval Ability to effectively
present ideas and document complex medical/clinical concepts in
both written and oral communication Understanding of resource and
budgeting 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 The expected annual salary range for this role in
the U.S. is $361,379 - $413,638.
Keywords: Msccn, Compton , Executive Medical Director Early Dev Inflammation - Thousand Oaks CA, Science, Research & Development , Thousand Oaks, California