Sr. Medical Director, Cell Therapy, Early Global Development, Oncology R&D

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. We have a bold ambition to provide cures for cancer in every form. We are following the science to understand cancer and all its complexities to discover, develop and deliver life-changing treatments and increase the potential to save the lives of people around the world. Join the team dedicated to Oncology, with an ambition to eliminate cancer as a cause of death. It’s our big vision that unites and inspires us.

We are seeking a Medical Director, with a focus on Cell Therapy, who is a clinician with strong leadership skills, driven by science and the desire to develop novel therapies for cancer patients. The Medical Director, Cell Therapy is accountable of the medical aspects related to cell and gene therapy trial conduct in multiple tumor indications across multiple geographies, The ideal candidate will have proficiency in the drug development process (especially early phase clinical trials), protocol writing & study conduct, data review and reconciliation, the principles of translational medicine, and what it takes to lead teams successfully. This individual will have the opportunity for growth and development while working in a vibrant environment by:

• Providing long-range clinical development planning, planning and managing of clinical research projects and clinical development programs in oncology

• Contribute to and support Department/Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional/organization processes designed to effectively deliver our R&D portfolio.

• Serve as medical monitor with primary responsibility for patient safety and conduct of assigned trials as well as overall data interpretation and safety surveillance

• Establish and approve scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports

• Responsible for assisting in design of clinical development plans and overall strategy for compounds, therapeutic classes of compounds or indications in light of developments in the area of clinical and pharmaceutical oncology

• Collaborate with pre-clinical and translational sciences, and senior management in assessing requirements for emerging products; Provide leadership on cross-functional product development team(s) as experience allows

• Participate in identification, selection and conduct of negotiations with clinical research centers and investigators;

• Participate in the selection and management activities of CROs; Supervise project team members in planning, conducting and evaluating clinical trials

• Lead all aspects of planning and management of investigator meetings, advisory boards and other scientific committees.

Minimum Qualifications:

• MD or MBBS degree and a professional qualification in Oncology and/or Hematology (Pediatric Onco-hematology allowed)

• Significant understanding of the overall drug development and commercialization process

• 3+ years of experience in clinical research and/or oncology drug development in pharmaceutical, academic or CRO environment.

• Conceptual, analytical, and strategic thinking

• Ability to influence strategically and persuade tactfully, to obtain desired outcomes while maintaining effective, positive, organizational relationships

Preferred Qualifications:

• MD/PhD in a scientific discipline related to immunology, oncology and/or gene therapy

• Experience in molecular oncology and/or translational science

• Medical specialty and subspecialty training and Board Certification

• Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment.

So, what’s next?

Are you already imagining yourself joining our team? Do you want to be part of building an innovative pipeline and deliver potentially high impact treatments to patients? If this describes you, submit an application today!

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The annual base pay (or hourly rate of compensation) for this position ranges from $265,780.80 to $398,671.20. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as 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.