Senior Director, Innovative Research Methods
Company: AstraZeneca
Location: Montgomery Village
Posted on: January 11, 2026
|
|
|
Job Description:
Do you have expertise in, and curiosity for driving innovation
in evidence generation in Oncology, including introduction of new
research methods, data collection approaches or the application of
GenerativeAI to improve operational efficiencies? Apply your
experience to changing the way cancer is treated at AstraZeneca, a
company that follows the science and turns ideas into life changing
medicines. Help to advance our incredible pipeline by applying
expertise and accelerating our pathway to finding a cure. The
NextGen Sciences (NGS) team is composed of highly functional
individuals with strong research skills, operating globally across
AstraZeneca’s brand and tumour areas to support the broader
Evidence Generation to Publications (EG2P) and Global Medical
Affairs organizationsin the identification of novel approaches for
evidence generation, including formation of global data assets,
streamlining prospective data collection efforts, and identifying
new paradigms forconducting research or generating impactful
communication. The Innovative Research Methods (IRM) function is a
key component of the NGS team, driving a ‘seed to sprout’ approach
for introducing new methods across the broader EG2P organization.
The Senior Director, IRMis responsible for: setting the innovation
agenda and identifying methods for downstream operationalization
that will improve the quality and turnaround time for clinical
studies conducted within EG2P, and the delivering impactful digital
and patient-focused solutions that support research for the
AstraZeneca oncology portfolio. This role will work collaboratively
to identify new opportunities for introducing innovation into our
new or ongoing Phase 3b/4 studies, externally sponsored research
(ESR) or Early Access Programmes (EAPs). Typical Accountabilities:
Be responsible for multiple initiatives within NGS and EG2P, and
therefore must be comfortable with ambiguity and able to flex
across different workstreams, cross-functional teams and discussion
topics. Conceive and pilotinnovations related to the conduct of
clinical studies, including recruitment, data collection, data
management or analysisthat enhance efficiencies or reduce burden
across multiple tumour types, geographies and settings. Lead
external academic partnerships, method co-development (e.g.,
external control arms, EMR-to-EDC pipelines, synthetic arms, DCT
design science), and cross-AZ alignment with R&D Biostatistics,
Data Science/ML, and Regulatory to ensure consistency and
scientific rigor Inform the development of plans and playbooks that
clearly outline key steps for implementationof
identifiedinnovations within current workstreams to increase
adoption across study teams. Collaborate closely with internal
global cross-functional partners including broader Evidence
Generation to Publications (EG2P) team, Oncology Medical Affairs
leadership and global Medical teams to enable implementation of new
/ innovative approaches to data collection, generation or
communication. Outline EG2P’s strategy for innovative digital
health or Artificial Intelligence (AI) solutions for evidence
generation (including use-cases, risk taxonomy, validation
frameworks, etc) and seek opportunities for innovation and
simplification. Be a thought partner inoptimizing data collection
in projects led by EG2P organization, such as Phase 3b/4 studies,
ESRs, or where applicable, EAPs, including publication of position
papers/guidance and contributions to industry standards Lead
discussions within broader AZ organization, including Research &
Development, regarding trends in clinical research innovation.
Provide leadership, mentor, feed forward to teams and individuals
to upskill and develop future capabilities in line with
AstraZeneca’s dedication to a culture of performance development
and lifelong learning. Lead stewardship of method qualification,
evidentiary standards, and regulatory engagement (e.g., dialogues
on RWE/external controls, DCT acceptability), ensuring methods meet
ICH/GCP and regional expectations before handoff to DIRA Education,
Qualifications, Skills and Experience Essential MS, PharmD or PhD
in relevant scientific subject area (outcomes research,
epidemiology, biostatistics) Minimum 10 years’ experience in the
pharmaceutical industry / consulting with proven track record in
clinical operations, clinical development, biostatistics, digital
healthor related subject areas. Ability to be creative and
collaborate on innovative research methods for conducting
prospective / clinical studies. Proven experience in conducting
innovative study approaches, including decentralized trials,
creation of external control arms, using EMR to EDC or digital
health tools for data collection. Recognized as a subject matter
authority with deep technical expertise with Phase 3b/4 clinical
trials, generation ofreal worldevidence, and HEOR projects Deep
understanding of Good Clinical Practice (GCP), US and Global
technical and regulatory requirements for conducting clinical
studies Strong verbal and written communication skills,
particularly related to conducting clinical research. Desirable
Scientific and business expertise in oncology with a strong
understanding of key global and regional issues and concerns.
Experience / knowledge of application of GenAI solutions within the
medical affairs or evidence generation fields Familiarity with the
latest research and thinking. Effective problem and conflict
resolution skills and validated team focus Proven track record of
operating within cross-functional / matrixed environment,
displaying ability to partner with other collaborators / teams. The
annual base pay (or hourly rate of compensation) for this position
ranges from $229,047 to $343,570. Our positions offer eligibility
for various incentives—an opportunity to receive short-term
incentive bonuses, equity-based awards for salaried roles and
commissions for sales roles. Benefits offered include qualified
retirement programs, paid time off (i.e., vacation, holiday, and
leaves), as well as health, dental, and vision coverage in
accordance with the terms of the applicable plans.
Keywords: AstraZeneca, Wilmington , Senior Director, Innovative Research Methods, Science, Research & Development , Montgomery Village, Delaware