Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians.  If you want to be part of this exciting work, you belong at Astellas!

 

Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com.

 

This position is based in Northbrook, Illinois. Remote work from certain states may be permitted in accordance with Astellas’ Responsible Flexibility Guidelines. Candidates interested in remote work are encouraged to apply.

 

Purpose and Scope:

This position is accountable for the oversight and execution of assigned pre/post-POC interventional drug programs, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approval access and post-marketing regulatory commitment trials (interventional and non-interventional).

 

This position is accountable to the Portfolio Operations Lead and clinical operations leadership team and will provide input into budget and resourcing strategies, including development and implementation of global processes and procedures, non-drug product initiatives, and mentoring and coaching of staff during execution of development trials.

 

This position has accountability for assuring strategic input and operational insight into the asset development planning lifecycle, including the Integrated Evidence Generation Plan (IEGP), Global Development Plan (GDP), Clinical Development Plan (CDP) and the implementation of patient-focused strategies for assigned programs.

 

Represents pre/post-POC Clinical Operations in Asset Teams, Portfolio and Operational review meetings, primary focus area governance, and cross-functional process improvement projects, as applicable. 

 

Individuals may serve in regional capacity to represent Clinical Operations in Key Opinion Leader (KOL) interactions, communications; Interactions and submissions to health authorities within their region/country of responsibility. 

This position may represent Clinical Operations in due diligence activities for assets that may be in-licensed or acquired.

 

Essential Job Responsibilities:

Responsible for effective planning, oversight, and execution of Clinical Development Plans and pre/post-POC trials for assigned assets and due diligence projects Ensures expert clinical operations strategy input is provided to Primary Focus Area and/or Asset Teams Develops clinical program budgets and resource estimates for assigned assets and due diligence projects Provides oversight of budget and resources during execution of clinical trials Provides oversight and guidance to extended team members in completing program deliverables according to agreed timelines and quality standards, including awareness and escalation of high impact quality-related topics for assigned programs Provides input on clinical operational matters for interactions with regulatory authorities and key opinion leaders, either globally or regionally, as applicable Participates in and/or facilitates cross-functional collaboration and strategic problem solving to ensure risk mitigation, appropriate progress and timely completion of trials and deliverables according to established objectives, milestones, and goals Works with teams to proactively identify and manage operational risks that arise during program and trial conduct, including escalation to Primary Operations Lead, functional management, and external vendor management to accelerate mitigation (as appropriate) Ensure close collaboration between Early and Late-Stage Clinical Operations Lead(s), including providing strategic and operational input during development and as the assets transition from early to late-stage development Individual can anticipate, recognize and drive problem solving to rapidly address and mitigate emerging program or trial risks Encourages individuals in investigating and applying clinical best practice methodologies in program(s) and clinical trials Represents Clinical Operations in inspection readiness activities including coordination of trial team quality deliverables Provide oversight and direction to trial team members for evaluation and implementation of patient-focused strategies for assigned trials Participates in resource allocation across the department as required for portfolio delivery and non-drug project initiatives/process improvements Acts as a change champion for Clinical Operations across the global organization Responsible for compliance of direct reports with Astellas policies, procedures, and all associated training

 

Quantitative Dimensions:

Responsible for overseeing the development and management of department and program budgets, resources and timelines for assigned assets

 

Organizational Context:

Reports to Portfolio Operations Lead or above Provides functional leadership and management globally of ≥ 3 direct reports, including international direct reports