Senior Group Director, Clinical Scientist at AstraZeneca

Gaithersburg, Maryland, United States -

Full Time

Start Date

Immediate

Expiry Date

18 Apr, 26

Salary

332250.0

Posted On

18 Jan, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Development, Hematology-Oncology, Global Study Leadership, Data Management, Clinical Trial Conduct, Scientific Writing, Analytical Skills, Stakeholder Engagement, People Leadership, Communication, Problem-Solving, Matrix Influence, Performance Management, Process Improvement, Mentorship, Collaboration

Industry

Pharmaceutical Manufacturing

Description

At AstraZeneca, we pride ourselves on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation – ultimately providing employees with the opportunity to work across teams, functions and even the globe. Recognizing the importance of individualized flexibility, our ways of working allow employees to balance personal and work commitments while ensuring we continue to create a strong culture of collaboration and teamwork by engaging face-to-face in our offices 3 days a week. Our dedication to sustainability is also central to our culture and part of what makes AstraZeneca a great place to work. We know the health of people, the planet and our business are interconnected which is why we’re taking ambitious action to tackle some of the biggest challenges of our time, from climate change to access to healthcare and disease prevention. The Role: The Senior Group Director, Clinical Scientist will lead a group clinical scientists within Hematology Research and Development and will also serve as a member of the Clinical Development leadership team. You will also be assigned to a project and are leading a team of clinical scientists and will be an important part of the project Team, working collaboratively with the program and study level physician or clinical lead as their guide in medical scientific aspects of the compound and its development. As a key member of the Global Project Team, this position demands strong collaborative communication skills, including the ability to engage with and influence a diverse range of business partners both within and external to AstraZeneca. You will drive and provide guide input to other non-assigned programs, process improvement initiatives, development of junior clinical scientists within Hematology and provides strategic contributions to the global clinical scientist team. In this role, you: Will be required to line lead other Clinical Scientists including project allocations/resource management, recruitment & selection, personal development and performance management May serve as the Skills Lead for the Clinical Science group thereby being responsible for ensuring appropriate procedures, training and personal development approaches are in place for the skill group and standard methodology is identified and implemented Contribute to the Departmental Leadership Team to ensure effective ways of working, identification and resolution of issues, departmental objective setting and may extend to prioritization and supervising at the departmental level Will lead or contribute to continuous improvement initiatives and may be required to run key alliances (provider and academic) Lead or supports clinical input to the clinical development plan at all stages of the program. Provide scientific/medical mentorship to the study team, including the CRO team. Follow important developments and trends in the medical & scientific literature and disseminates updates to the project team and beyond ensuring all involved parties are aware of key developments and the impact on the strategy Leads the development and review of content and quality of publications and inputs to development of the publication strategy Guide aspects of the Clinical Development Plan (CDP) and Clinical Study Protocols in keeping with the approved CDP and ensuring linkage of trial data to target product profile Attend (in person or by TC) the Site Initiation Visits, to present the study design and key aspects of the protocol Lead (or supports as required), clinical data review and interpretation of the study and program level with input from the study or program Physician/Clinical Lead Own the compilation and interpretation of the data for and from the dose escalation committee/safety review committee, in collaboration with the program physician Provide input for the protocols, amendments, Investigator Brochure, DSURs and other relevant strategic documents. Acts as lead clinical reviewer for Clinical Study Reports Support due diligence activities for potential in-licensing or collaborative opportunities and provides recommendations to senior management Drives key critical initiatives within and beyond the Hematology Clinical Development group Develops, coaches, mentors, motivates and encourages individuals within the organization Operates in compliance with GCP and relevant regulatory guidelines. Essential Requirements: Advanced degree: PhD or PharmD with 12+ years of relevant industry experience and a proven track record in clinical development. Therapeutic expertise: Extensive knowledge of GCP and end-to-end drug development (Phases I–III), with a strong preference for Hematology-Oncology. Global study leadership: Significant experience designing, organizing, and executing global clinical studies in pharma/biotech environments. Data and systems proficiency: Deep understanding of clinical data collection and reporting; advanced proficiency with data management systems and analytical tools, with a demonstrated ability to optimize processes and drive continuous improvement. Clinical trial Conduct: Robust experience managing and interpreting clinical trial results, with strong exposure to protocol development and writing. Scientific writing: Experience authoring scientific documents (e.g., protocols, study reports, publications). Analytical strength: Strong analytical and problem‑solving skills with the ability to translate insights into decisions. Matrix influence: Proven ability to work effectively in a matrixed environment and influence stakeholders at all levels without direct authority. Execution under pressure: Demonstrated success prioritizing and delivering under tight deadlines while maintaining high quality standards. Communication: Excellent verbal and written communication skills in English; able to communicate complex information clearly and drive alignment and efficiency. Stakeholder engagement: Sufficient technical and disease area knowledge to interact confidently with internal and external partners. People leadership: Proven track record of line management, including coaching and performance development. Language: High proficiency in English (written and spoken). Are you interested in working at AZ, apply today! AstraZeneca is an equal opportunity employer that is committed to diversity and inclusion and providing a workplace that is free from discrimination. AstraZeneca is committed to accommodating persons with disabilities. Such accommodation is available on request in respect of all aspects of the recruitment, assessment and selection process and may be requested by emailing AZCHumanResources@astrazeneca.com. The annual base pay for this position ranges from $221,500 to $332,250 USD. 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. #LI-Hybrid Date Posted 17-Jan-2026 Closing Date 30-Jan-2026 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. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Responsibilities

The Senior Group Director, Clinical Scientist will lead a team of clinical scientists within Hematology Research and Development and contribute to the Clinical Development leadership team. This role involves guiding clinical input for development plans and ensuring effective collaboration across various teams.