Title: Senior Director Physician, Hematology SKG Lead
Location: Boston or Gaithersburg
What will you do:
The clinical Hematology Safety Knowledge Group (SKG) Lead manages a diverse range of activities related to monitoring, diagnosis, and mitigation of drug/biological-induced hematologic toxicity in a matrix environment. The haematology safety expert develops and leads the Hematology SKG, a multidisciplinary team responsible for evaluation and interpretation of potential safety signals, development of proactive and reactive minimization measures related to hematologic toxicity, including development of best practices to mitigate risk to patients.
The role holder inspires, manages, and leads cutting edge drug/biological-induced hematologic toxicity projects on a global basis. The Hematology SKG Lead will be influencing the shaping of the organisation by providing strategic direction and applying a full understanding of global issues related to drug/biological-induced hematologic toxicity. The role impacts the entire function and the broader AZ organization.
Accountabilities:
- Acts as expert involved in the design, conduct, monitoring, data interpretation and reporting of potential clinical safety signals related to hematologic toxicity which arise during the conduct of clinical trials.
- Acts as expert in hematologic safety/toxicity to provide scientific and medical input to Global Patient Safety (GPS) activities, with special focus on cross-project and cross-TA activities of a scientific nature.
- Provides specialist clinical Hematology advice to AZ project teams consulting with the Hematology SKG
- Leads co-ordination of clinical input to Hematology SKG work internally and to external initiatives.
- Drives scientific research around drug-induced hematologic toxicity, ensuring the research projects related to drug-induced hematologic toxicity adhere to Good Clinical Practice and regulatory requirements.
- Leads development of strategies to ensure that scientific assessment, mitigation and prevention of risk to patients are on a leading pharmaceutical industry level
- Leads and endorses the development of scientific methods applied to a wide range of safety data related to hematologic toxicity and potential toxicities in new therapies/novel modalities with potential hematologic toxicity concerns.
- Incorporates current, up-to-date understanding of clinical hematology practice and literature.
- Leads the development of drug/biological-induced hematologic toxicity biomarkers/assessments
- Leads initiatives to increase cross-company knowledge of drug-induced hematologic toxicity through training and other activities
- Drives projects to enhance visualisation and presentation of hematologic toxicity/safety data
- Provides support, as needed, for discussions with internal governance and international regulatory bodies
- Contributes to develop better understanding and prevention of hematology toxicity/safety issues across functions within the company and across Pharmaceutical Companies and Regulatory Authorities.
- Has a strong presence at internal and external conferences and delivers key scientific publications
- Promotes safety sciences and clinical safety across projects and therapeutic areas
Essential skills:
- Medical degree or equivalent experience with strong clinical experience
- Specialty training in clinical hematology, board certification in the field of expertise, with > 5 years of clinical practice
- Proven Continuing Medical Education activities in the field of clinical hematology
- Solid knowledge of the pharmaceutical industry, drug development, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
- Proven high quality scientific track record
- High level of interactive communication to set clear direction and directly advising others at a high level
- Enhanced cultural sensitivity to leading teams in a matrix environment
- Ability to balance business and clinical research objectives
- Excellent verbal and written communication skills
- Experience in leading cross-functional teams
- Strategic thinking
- Strategic influencing
Desirable skills:
- > 3 years of drug development and safety experience, the majority of which should be in industry, with clear evidence of delivery
- Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions
- Understanding of specialty- specific requirements at various stages of lifecycle development and relevant regulatory guidance
- Demonstrated capability to lead implementation of new guidance and/or working routines within a complex organization in response to new or novel problems
- Extensive general medical knowledge and academic/research experience
- Involvement in relevant professional society activities, involvement at national/international meetings, and contributions to the literature
- Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
The annual base pay (or hourly rate of compensation) for this position ranges from $265,781 to $398,671. 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.
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 authorization and employment eligibility verification requirements.
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