Associate Director / Director Study Leader, Cell Therapy

Do you have a passion for Science? Would you like to apply your expertise to impact a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you!

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.

At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most sophisticated diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

Position Summary

The Director Study Leader, Cell Therapy delivers a single or several smaller Cell Therapy development programs or leads multiple Cell Therapy studies or single complex/novel studies such as platform, basket. The exact accountabilities will differ depending on the nature of the clinical studies or program. You will report to the Sr. Director Group Leader, Cell Therapy or equivalent.

The Director Study Leader, Cell Therapy may provide authoritative input to other non-drug programs and process improvement projects.

Supervisory Responsibilities

• May have 5 direct/indirect reports

Responsibilities

• Provide guide clinical operational input into project or study level documents and may lead the delivery of study documents.

• With oversight from the Clinical Program Director, Cell Therapy may lead and deliver outstanding and operational options for review at Investment Decision Governance interactions.

• Lead the delivery of the clinical study(s) or program(s) from concept to final CSR and through to study closed and archived to agreed budget, time, project standards, quality and scientific standards

• Lead and optimize the performance of study delivery teams ensuring GCP compliance, including provision of and accurate performance feedback for study team members to the appropriate AZ manager or CRO representative

• Accountable for overall study or program deliverables, maintaining oversight throughout the life of the study or program.

• Implement agreed study level process and technology for assigned Cell Therapy clinical studies.

• Lead risk management/mitigation plans to ensure delivery to quality, budget and time and raise issues to partners

• Provide input to forecasting and management of study delivery costs, resource, and timelines

• Accountable for the quality of study/program planning information into relevant planning systems (e.g, PLANIT) in collaboration with counterpart in relevant therapeutic area

• May guide the Study Team in the development of outsourcing specifications and vendor selection.

• Provision to procurement clear specifications for study or program specific outsourcing

• Perform review and operational approval of study or program specific contracts or work orders

• Responsible for oversight of CROs and other clinically outsourced third-party vendors

• Communicate study level reports and status updates for assigned Cell Therapy studies, including progress issues

• Lead risk management and quality efforts to ensure study compliance and inspection readiness for apheresis and cell therapy infusion activities

• May lead the study delivery related activities associated with regulatory inspections/audits in liaison with Clinical QA for apheresis and cell therapy infusion activities

• Contribute to operational interactions with external entities including regulatory agencies, preferred partners/suppliers, and external collaborators

• Be responsible for the submission of trial-rcruciald essential documents to the Trial Master File, maintenance and final closeout.

Experience and Education:

Associate Director: Bachelor's degree in related field in medical or biological science. Must have at least 8 years drug development experience demonstrated in multiple role and 3 years of experience leading studies/programs in clinical development. Minimum 3 years of direct Cell Therapy experience

Director Level: Bachelor's degree in related field in medical or biological science Must have at least 10 years drug development experience demonstrated in multiple roles and 5 years of experience leading studies/programs in clinical development. Minimum 3 years of direct Cell Therapy experience

Required Skills:

• Extensive knowledge of the clinical drug development process

• Experience leading delivery through internal and external organizations.

• Excellent knowledge of ICH-GCP principles

• Experience in selection and oversight of external providers and development/providing clear requirements of contracts

• Experience in variety of academic/CRO/Sponsor organizations and countries

• Experience of early phase clinical delivery and in autologous or allogeneic therapies in oncology

When we put unexpected teams in the same room, we fuel bold thinking with the power to encourage 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.

The annual base salary for this position ranges from $126,805 to $212,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related experience. If hired, employee will be in an "at-will position" and we reserve the right to modify base salary (and any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, groundbreaking powerful methods and bringing unexpected teams together. Interested? Come and join our journey.

So, what’s next!

Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.

Where can I find out more?

Check out our landing page for more information on our BPD group  https://careers.astrazeneca.com/bpd

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AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.