Senior Director, Clinical Operations Strategic Enablement R&I
Astrazeneca, Toledo, Ohio, United States, 43614
Senior Director, Clinical Operations Strategic Enablement
TheSenior Director, Clinical Operations Strategic Enablement will lead the design, build, innovation and continuous improvement ofclinical operations capabilities to support the delivery of clinical development programs in the R&I and V&I Therapeutic Area. They will partner cross-functionally within Clinical Operations, Clinical Development, Medical Affairs, Commercial, other aligned internal functions and external partners to lead the collation of data insights to support clinical trial design in new disease areas and strengthen investigator/site identification and engagement. Working with R&I and V&I TA strategy, the role will support identification and connection of data sources to champion data driven, patient-centric practices that improve trial design, performance, study start‑up, recruitment, and data quality. This global role provides deep understanding of historical trends, industry benchmarks and cycle times to drive acceleration, innovative approaches, inform planning, portfolio oversight and performance management, including milestone tracking, KPI development and monitoring. This senior leader brings extensive clinical operations portfolio leadership, strong stakeholder collaboration and strategic thinking to drive innovative, effective trial design and delivery for R&I indications.
Accountabilities
Planning, Governance and Analytics: Collating historical trends, industry benchmarks and cycle times to define KPIs and identify opportunities for improved performance, innovation and continuous improvement
Partner in development of data standards, metrics and dashboards to facilitate use of information providing business insights and informed decision making relating to trial design and execution to support clinical operations leadership/department
Support long‑range planning through provision of Clinical Operations data insights and metrics during Therapeutic Area (TA) strategy, Medium‑Term Plan (MTP), and Long‑Term Plan (LTP), embedding operational considerations and feasibility insights into strategic decision‑making for new and emerging indications
Facilitate discussions in monthly resource reviews and performance insights on clinical portfolio
Identify opportunities to leverage technology, AI and automation and support adoption across the R&I Clinical Operations department
Align and share data insights and expertise cross‑functionally
TA Strategy
Collate insights to inform study design and delivery team planning considering specific therapy area standards of care, regulations and advancements in practice
Define the vision, and roadmap for building R&I clinical operations capabilities to support new and established indications, innovative trial design and technologies
Partner in oversight of the work of Clinical Trial Liaisons and Clinical Trial Educators (if utilized), setting priorities, providing coaching, and monitoring performance to ensure consistent, high‑quality execution
Disease area and site network development
Lead set‑up and execute a comprehensive investigator engagement strategy for new and established R&I indications covering scientific exchange, operational enablement, performance feedback, recognition and long‑term partnership models
Support cross‑functionally in development of high‑performing, diverse global investigator and site networks to deliver development programs in new and established R&I indications
Ensure aligned engagement across SMM, Clinical Development, Medical Affairs, and Commercial and ensure consistent messaging across these groups on R&I portfolio priorities
Coordinate Therapeutic Area R&D‑focused congress activities, including planning, content alignment, stakeholder preparation, and post‑congress follow‑up to translate insights into operational actions
Essential
Scientific/technical (e.g. BS, MS) or PhD, PharmD)
10+ years' experience in drug development, clinical trial conduct, clinical operations, and site level interactions including experience in clinical development (pharmaceutical industry, CRO, or academia)
Portfolio leadership experience across early and late phase stages and change management
Proven experience in data analysis and depth of knowledge in clinical operations data insights
Experienced in project and budget management technologies and process
Proven ability to develop successful collaborations with internal stakeholders and external partners
Excellent communication skills and stakeholder management
Ability to influence in a matrixed, ambiguous environment
Strong strategic influencing skills, innovative, and adept at effectively solving complex problems.
Knowledge and experience to work across projects, with a fast‑learning curve when moving into new disease areas
Proven track record of self‑management, planning, prioritization, and delivery success
Behaviors
Ability to develop and maintain strong customer and business partner relationships
Flexibility to work in a fast‑paced and constantly changing environment
Demonstrated leadership qualities with focus on collaborative working skills, prioritization, trust, and openness – irrespective of cultural setting
Proven teamwork and collaboration skills
Demonstrates AstraZeneca Values and Behaviors
Desirable
Experience in either respiratory or allergy/immunology/autoimmune diseases
Experience in matrix team environment with interplay between clinical, operations, commercial, drug safety and regulatory
Experience of working with external specialty providers, clinical sites, and patient advocates
Experience of working as part of a clinical trial team within a clinical site
Knowledge and capability with digital solutions/tools
Benefits and Compensation The annual base pay for this position ranges from $233,586.40 to $350,379.60. 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.
Work Environment When we put unexpected teams in the same room, we ignite bold thinking with the power to inspire life‑changing medicines. In‑person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca Here, work is driven by the real journeys of people living with rare and devastating diseases, and your decisions will contribute directly to therapies that matter. We pair the agility of a biotech mindset with the reach and resources of a global biopharma, empowering you with cutting‑edge science, data, and collaboration tools. We value kindness alongside ambition, bringing diverse thinkers together to challenge conventions and build better solutions for patients. You will grow with peers and leaders who invest in your development and trust you to lead with integrity, inclusiveness, and scientific excellence.
Call to Action Step into this Medical Director role to steer neurology programs that change lives and see your leadership turn rigorous science into real‑world impact.
Date Posted 27-Jan-2026
Closing Date No closing date specified.
EEO Statement Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
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Accountabilities
Planning, Governance and Analytics: Collating historical trends, industry benchmarks and cycle times to define KPIs and identify opportunities for improved performance, innovation and continuous improvement
Partner in development of data standards, metrics and dashboards to facilitate use of information providing business insights and informed decision making relating to trial design and execution to support clinical operations leadership/department
Support long‑range planning through provision of Clinical Operations data insights and metrics during Therapeutic Area (TA) strategy, Medium‑Term Plan (MTP), and Long‑Term Plan (LTP), embedding operational considerations and feasibility insights into strategic decision‑making for new and emerging indications
Facilitate discussions in monthly resource reviews and performance insights on clinical portfolio
Identify opportunities to leverage technology, AI and automation and support adoption across the R&I Clinical Operations department
Align and share data insights and expertise cross‑functionally
TA Strategy
Collate insights to inform study design and delivery team planning considering specific therapy area standards of care, regulations and advancements in practice
Define the vision, and roadmap for building R&I clinical operations capabilities to support new and established indications, innovative trial design and technologies
Partner in oversight of the work of Clinical Trial Liaisons and Clinical Trial Educators (if utilized), setting priorities, providing coaching, and monitoring performance to ensure consistent, high‑quality execution
Disease area and site network development
Lead set‑up and execute a comprehensive investigator engagement strategy for new and established R&I indications covering scientific exchange, operational enablement, performance feedback, recognition and long‑term partnership models
Support cross‑functionally in development of high‑performing, diverse global investigator and site networks to deliver development programs in new and established R&I indications
Ensure aligned engagement across SMM, Clinical Development, Medical Affairs, and Commercial and ensure consistent messaging across these groups on R&I portfolio priorities
Coordinate Therapeutic Area R&D‑focused congress activities, including planning, content alignment, stakeholder preparation, and post‑congress follow‑up to translate insights into operational actions
Essential
Scientific/technical (e.g. BS, MS) or PhD, PharmD)
10+ years' experience in drug development, clinical trial conduct, clinical operations, and site level interactions including experience in clinical development (pharmaceutical industry, CRO, or academia)
Portfolio leadership experience across early and late phase stages and change management
Proven experience in data analysis and depth of knowledge in clinical operations data insights
Experienced in project and budget management technologies and process
Proven ability to develop successful collaborations with internal stakeholders and external partners
Excellent communication skills and stakeholder management
Ability to influence in a matrixed, ambiguous environment
Strong strategic influencing skills, innovative, and adept at effectively solving complex problems.
Knowledge and experience to work across projects, with a fast‑learning curve when moving into new disease areas
Proven track record of self‑management, planning, prioritization, and delivery success
Behaviors
Ability to develop and maintain strong customer and business partner relationships
Flexibility to work in a fast‑paced and constantly changing environment
Demonstrated leadership qualities with focus on collaborative working skills, prioritization, trust, and openness – irrespective of cultural setting
Proven teamwork and collaboration skills
Demonstrates AstraZeneca Values and Behaviors
Desirable
Experience in either respiratory or allergy/immunology/autoimmune diseases
Experience in matrix team environment with interplay between clinical, operations, commercial, drug safety and regulatory
Experience of working with external specialty providers, clinical sites, and patient advocates
Experience of working as part of a clinical trial team within a clinical site
Knowledge and capability with digital solutions/tools
Benefits and Compensation The annual base pay for this position ranges from $233,586.40 to $350,379.60. 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.
Work Environment When we put unexpected teams in the same room, we ignite bold thinking with the power to inspire life‑changing medicines. In‑person working gives us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
Why AstraZeneca Here, work is driven by the real journeys of people living with rare and devastating diseases, and your decisions will contribute directly to therapies that matter. We pair the agility of a biotech mindset with the reach and resources of a global biopharma, empowering you with cutting‑edge science, data, and collaboration tools. We value kindness alongside ambition, bringing diverse thinkers together to challenge conventions and build better solutions for patients. You will grow with peers and leaders who invest in your development and trust you to lead with integrity, inclusiveness, and scientific excellence.
Call to Action Step into this Medical Director role to steer neurology programs that change lives and see your leadership turn rigorous science into real‑world impact.
Date Posted 27-Jan-2026
Closing Date No closing date specified.
EEO Statement Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
#J-18808-Ljbffr