Global Development Medical Director

AstraZeneca; Gaithersburg (MD); On-site; USD 250,000 - 375,000; Full time

Job summary

AstraZeneca in Gaithersburg, MD seeks a Global Development Medical Director to drive medical and scientific leadership for late-phase CVRM trials. You will design, monitor, interpret, and report data to support labeling and pricing across markets.

The role requires 3+ years in clinical research, a medical degree or PhD, and fluency in English, with strong communication, leadership and team collaboration skills. Office-based in Gaithersburg with global collaboration.

Qualifications

• Medical degree or PhD in a scientific discipline with regulatory knowledge.
• 3+ years of clinical research expertise in relevant therapy areas.
• Strong knowledge of biostatistics, global regulatory environment and pharmacovigilance.
• Proven teamwork and collaboration skills; fluent in English.
• Excellent presentation and communication abilities.

Responsibilities

• Provide strategic medical and scientific expertise for study design and execution in CVRM/NASH.
• Drive study design decisions and deliver medical information to regulators and investigators.
• Ensure compliance with GCP, safety reporting and study documentation.
• Collaborate with global colleagues and alliance partners across R&D sites.
• Lead induction and education of new study team members and ensure risk mitigation.

Skills

Leadership

Teamwork

Communication

English fluency

Education

Medical degree (M.B.B.S./M.D.)

PhD or equivalent in scientific discipline

Job description

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.

Welcome to Gaithersburg, MD one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities, it’s important to us that you bring your full self to work every day. To help you maintain your best self, here’s a sneak peek into some of the things this site provides for you…g"ym access, after-work events, lunch & learns, bright and spacious environment, sustainable office working environment and networking events.

As a Global Development Medical Director in Gaithersburg, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. The successful Study Clinical Lead in Late Phase CVRM (Cardiovascular, Renal, and Metabolic diseases) will be responsible for the design, conduct, monitoring, data interpretation and reporting of individual clinical trials ensuring that the clinical data collected within the study will allow determination of the benefits and risks of the compound, as well as will allow for the intended label indication and price in markets globally. The individual will operate according to the highest ethical standards in compliance with internal SOPs, local regulations, laws, Good Clinical Practice, and regulatory requirements.

Responsibilities/Accountabilities

Medical expert accountabilities

• Provides strategic medical and scientific knowledge (Cardiovascular, Renal, and/or NASH) and supports the design, initiation, execution, completion, and interpretation of a clinical study
• Is accountable for study designs
• Is accountable to deliver medical information, answers, and clarifications to Regulators, Ethic Committees, Marketing Companies, Investigators/Sites

Trial Conduct And Hands-on Delivery Accountabilities

• Is accountable to the Global Clinical Head (GCH) or delegate for the medical aspects and designs of studies
• Is responsible for driving decisions within Study Team (ST) remits together with other ST members and for solving medical issues in the study team
• Is accountable for the medical and ethical components of studies including patient safety on a study level in compliance with GCP
• Is accountable for delivery of all relevant study documents (e.g Protocol, Amendments, Statistical Analysis Plan, Informed Consent Form, Case Report Forms, and Safety and Risk-Based Monitoring Plans)
• Is accountable for safety surveillance on a study level including the process for Adverse Events (AE)/ Serious AE reporting, the querying of missing/unclear data, the review of blinded safety data, and the escalation to the GCH/Global Safety Physician when needed.
• Is medically accountable for international investigator meetings, and supports Marketing Companies (MC) in national activities
• Approves (with the GCH) the Clinical Study Report; including preparation and production thereof (Introduction, Results, Discussion).
• Is accountable for ST induction and education of new members in the study team, as well as others involved in the study
• Collaborates seamlessly and efficiently with global colleagues at other R&D sites
• May be accountable to GCH (or delegate) and leadership for identifying risks and proposing mitigation strategies to deliver successful Phase II, III, IV or Life Cycle Management studies

Scientific Medical Analytical Accountabilities

• Stays updated on relevant scientific literature
• Delivers analyses of clinical data in a balanced, statistically sound fashion, to drive interpretations and further idea generation
• Serves as a source of medical expertise for the Product Team, in analyses and interpretation of medical data

Messaging And External Impact Accountabilities

• Maintains a high degree of understanding and awareness on new and emerging medical development, globally.
• Works with international colleagues and with external Alliance partners on development initiatives and regulatory issues
• Applies strategic intent of AstraZeneca when working with Alliance partners, Regulatory Authorities, payers, opinion leaders, prescribers and consumers of AstraZeneca products
• Able to provide guidance for investigator-initiated trials in cooperation with regional marketing companies

Minimum Requirements

• Graduate of a recognized school of medicine with an M.B.B.S., M.D. degree or equivalent, and/or a graduate of a scientific doctorate (e.g. PhD ) or equivalent in a scientific discipline or Pharmaceutical Medicine
• 3+ years clinical research expertise in relevant therapy area in study design, protocol development, monitoring and implementing clinical trials, interpreting and reporting trial results
• Good knowledge of biostatistics, global regulatory environment and pharmacovigilance
• Proven teamwork and collaboration skills
• Fluent in oral and written English
• Good presentation skills and effective communication

A Clear Demonstration Of

• Leadership qualities, with particular focus on collaborative working skills, trust and openness, irrespective of cultural setting
• AstraZeneca values and behaviors
• Agile responsiveness to scientific data
• Credibility in scientific and commercial environments

Desired Experience

• Good general medical knowledge preferably in nephrology or NASH
• An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence drug development
• An understanding of the interplay between clinical, commercial objectives, drug safety and regulatory requirements

The annual base salary for this position ranges from $249,827.00 to $374,740.00. However, 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).

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire 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. But that doesn't mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

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, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey.

So, what’s next!

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

Where can I find out more?

Our Social Media, Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/

Follow AstraZeneca on Facebook https://www.facebook.com/astrazenecacareers/

Follow AstraZeneca on Instagram https://www.instagram.com/astrazeneca_careers/?hl=en

Date Posted

17-Aug-2026

Closing Date

29-Oct-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.