Strong knowledge of the drug development process, GCP/ICH guidelines, and relevant regulatory requirements; Significant operational experience in the planning, delivery, and oversight of clinical ...
Strong knowledge of the drug development process, GCP/ICH guidelines, and relevant regulatory requirements; Significant operational experience in the planning, delivery, and oversight of clinical ...
Strong knowledge of the drug development process, GCP/ICH guidelines, and relevant regulatory requirements;Significant operational experience in the planning, delivery, and oversight of clinical ...
New
Strong knowledge of the drug development process, GCP/ICH guidelines, and relevant regulatory requirements;Significant operational experience in the planning, delivery, and oversight of clinical ...
New
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences andClinical Development(TSCD)team, we are investigating the drivers of ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences andClinical Development(TSCD)team, we are investigating the drivers of ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249.83 - $374.74/hr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249.83 - $374.74/hr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Sr. Principal Scientist (Sr. Director) - Regulatory Liaison
Rockville, MD · On-site
$152K - $201K/yr
S., with minimum of 10 years relevant drug development experience, with a majority in regulatory affairs * M.S. with minimum of 10 years relevant drug development experience, with a majority in ...
Sr. Principal Scientist (Sr. Director) - Regulatory Liaison
Rockville, MD · On-site
$152K - $201K/yr
S., with minimum of 10 years relevant drug development experience, with a majority in regulatory affairs * M.S. with minimum of 10 years relevant drug development experience, with a majority in ...
TypicalAccountabilities Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical research ...
New
TypicalAccountabilities Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical research ...
New
Senior Scientist I, Method Development
Germantown, MD · On-site
$95K - $115K/yr
Senior Scientist I, Method Development Location: Germantown, MD Compensation: $95k - $115k About ... drug discovery through to manufacturing with fully integrated high-quality services. We're proud of ...
Senior Scientist I, Method Development
Germantown, MD · On-site
$95K - $115K/yr
Senior Scientist I, Method Development Location: Germantown, MD Compensation: $95k - $115k About ... drug discovery through to manufacturing with fully integrated high-quality services. We're proud of ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Medical Director, Respiratory, Early Clinical Development
Gaithersburg, MD · On-site
$249K - $374K/yr
If you are a motivated drug developer, this is an excellent time to join! Who We Are In the Respiratory Translational Sciences and Clinical Development (TSCD) team, we are investigating the drivers ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
Key Responsibilities Drug Product Platform Development Strategy * Help to define and execute the long-term drug product platform strategy for lentiviral vectors supporting AstraZeneca's In-vivo Cell ...
... drug discovery through to manufacturing with fully integrated high-quality services. We're proud of ... Lead day-to-day method development activities for assigned preclinical and clinical programs.
... drug discovery through to manufacturing with fully integrated high-quality services. We're proud of ... Lead day-to-day method development activities for assigned preclinical and clinical programs.
Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases
Rockville, MD · On-site
$210K - $331K/yr
D. with minimum of 3 years relevant drug development or clinical experience required, or * Ph.D. with minimum of 5 years relevant drug development experience required, or * M.S. with minimum of 7 ...
Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases
Rockville, MD · On-site
$210K - $331K/yr
D. with minimum of 3 years relevant drug development or clinical experience required, or * Ph.D. with minimum of 5 years relevant drug development experience required, or * M.S. with minimum of 7 ...
Typical Accountabilities • Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical ...
Typical Accountabilities • Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical ...
Typical Accountabilities • Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical ...
Typical Accountabilities • Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical ...
Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases
Rockville, MD · On-site
$152K - $201K/yr
D. with minimum of 3 years relevant drug development or clinical experience required, or * Ph.D. with minimum of 5 years relevant drug development experience required, or * M.S. with minimum of 7 ...
Director, Regulatory Affairs Liaison, Vaccines & Infectious Diseases
Rockville, MD · On-site
$152K - $201K/yr
D. with minimum of 3 years relevant drug development or clinical experience required, or * Ph.D. with minimum of 5 years relevant drug development experience required, or * M.S. with minimum of 7 ...
Associate Director/Senior Manager Regulatory Affairs
Germantown, MD · On-site
$150K - $180K/yr
This role is responsible for knowledge and application of global regulations governing pharmaceutical drug development. Working with the Vice President, Regulatory Affairs this position will ...
Quick apply
Associate Director/Senior Manager Regulatory Affairs
Germantown, MD · On-site
$150K - $180K/yr
This role is responsible for knowledge and application of global regulations governing pharmaceutical drug development. Working with the Vice President, Regulatory Affairs this position will ...
Are you ready to be part of the solution, turning drug development strategies into reality? As an Associate Director in Clinical Regulatory Writing, you'll play a pivotal role in translating life ...
Are you ready to be part of the solution, turning drug development strategies into reality? As an Associate Director in Clinical Regulatory Writing, you'll play a pivotal role in translating life ...
Drug Development information
See Washington, DC salary details
$37.4K - $47.7K
2% of jobs
$47.7K - $58K
8% of jobs
$65.8K is the 25th percentile. Wages below this are outliers.
$58K - $68.3K
19% of jobs
$68.3K - $78.6K
20% of jobs
The median wage is $78.9K / yr.
$78.6K - $88.9K
16% of jobs
$96.8K is the 75th percentile. Wages above this are outliers.
$88.9K - $99.2K
13% of jobs
$99.2K - $109.4K
5% of jobs
$109.4K - $119.7K
11% of jobs
$119.7K - $130K
2% of jobs
$130K - $140.3K
2% of jobs
$140.3K - $150.6K
2% of jobs
$37.4K
$87.7K
$150.6K
How much do drug development jobs pay per year?
What career develops drugs?
What is the difference between Drug Development vs Pharmacologist?
| Aspect | Drug Development | Pharmacologist |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related fields; often requires experience in clinical trials | Degree in Pharmacology, Pharmacy, or related fields; may require licensing or certification for clinical practice |
| Work Environment | Research labs, pharmaceutical companies, clinical trial sites | Research labs, hospitals, academic institutions, regulatory agencies |
| Industry Usage | Developing new drugs, overseeing clinical trials, regulatory submissions | Studying drug effects, mechanisms, safety, and efficacy; advising on drug use |
While both roles are integral to the pharmaceutical industry, Drug Development focuses on creating and bringing new drugs to market through research, testing, and regulatory processes. Pharmacologists primarily study how drugs interact with biological systems, often working in research or clinical settings to understand drug effects and safety. The two roles often collaborate but differ in their core responsibilities and career focus.
What are the key skills and qualifications needed to thrive in drug development, and why are they important?
What is drug development?
How much do drug development professionals make?
How do you get into drug development?
What are the typical stages of collaboration between different teams in a drug development role?
- Director Of Development And Communications
- Associate Medical Director Clinical Development
- Director Leadership Development
- Business Affairs Remote
- Director Proposal Development
- Sr Director Of Business Development
- Director Of Technical Development
- Senior Political Fundraising
- Cmc Msat Director Biologics
- Associate Director Biopharma Pharmaceutical

Full-time
Posted 4 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
22nd of 86 rated pharmaceutical
Job description
Externally recognized as a thought leader with deep expertise in both clinical research and development with deep understanding of autoimmune disease, specifically inflammatory myopathies, JIA and/or Sjogren's disease. Knowledge and expertise in cell therapy is a plus. Drive the integrated clinical research and development strategy and execution, to ensure value creation and regulatory/market success through innovative, cross-functional leadership. Operate independently and at scale, influencing both operational excellence and strategic direction at the highest organizational levels.
Typical Accountabilities
• Develop and align strategies and objectives for Clinical Research & Development, ensuring they support AstraZeneca's global goals and product vision.
• Lead and oversee execution and delivery of clinical research & development studies, ensuring scientific rigor, commercial viability, and patient-centric focus throughout the drug lifecycle.
• Lead the work with Line Managers to identify resource need and secure resources to ensure flexible and timely formation of the Clinical Research & Development Teams and progression of deliverables
• Provide strategic and operational input to ensure implementation of best practices, new technologies, processes, and global clinical strategies.
• Manage resource planning in collaboration with line managers, securing talent and flexible teams to support dynamic project requirements.
• Oversee budgeting, timelines, contingency and risk management planning, and escalate operational or strategic issues as appropriate.
• Lead the negotiation and management of contracts with CROs and external service providers.
• Drive the preparation, review, and delivery of regulatory submission materials and actively participates in regulatory defense/approval processes.
• Has personal responsibility for creating a culture of courageous leadership, creativity and collaboration
• Mentor, develop, and manage performance of line management and project teams, ensuring alignment with organizational goals and fostering succession planning.
• Ensure all work is compliant with internal and external standards, including Safety, Health, Environment, and regulatory guidelines.
Qualifications and Skills
- Essential: Advanced degree (Master's, PhD, or equivalent) in a scientific, medical, or health-related discipline; Extensive experience in both clinical research and clinical development within the pharmaceutical or biotechnology industry; Familiarity with the scientific and clinical community; Proven leadership experience managing cross-functional and/or senior project teams; Demonstrated success in strategy development and execution in both clinical research and clinical development environments; Strong knowledge of the drug development process, GCP/ICH guidelines, and relevant regulatory requirements; Significant operational experience in the planning, delivery, and oversight of clinical trials and regulatory submissions; Budgetary, resource, and risk management expertise on a global or regional scale; Exceptional written and verbal communication skills and ability to present to diverse stakeholders; Demonstrated ability to mentor, develop, and lead teams; Highly skilled in stakeholder engagement, negotiation, strategic influencing, and cross-functional collaboration; Commitment to compliance and safety, health, and environmental standards; Ability and willingness to travel nationally and internationally as required
- Desirable: Experience as a recognized expert or thought leader within the business and wider industry; Project management certification or formal training; Experience in the introduction or implementation of new technologies or innovative approaches within clinical research or development; Experience in change management and process improvement initiatives; Experience managing complex organizational structures or leading in a global organizational context; Extensive familiarity with key therapeutic areas relevant to AstraZeneca's portfolio; Record of effective succession planning and leadership development within multi-level teams; Experience in successful regulatory defense and participation in external advisory boards or similar expert panels; Advanced negotiation and contracting experience with CROs or external service providers; Ability to identify and leverage emerging trends in drug development, technology, and scientific innovation
Key Relationship to Reach Solutions
- Internal: Study Delivery personnel; Data Management Centre representatives; Clinical Project Team and therapy area personnel; Clinical Development personnel; Clinical Pharmacology Units; Study Site personnel; Regional Monitoring personnel; Other Skill Centres as appropriate
- External: External service providers; Investigators and scientists and patient advocacy groups; and external Alliance partners
Date Posted
09-Aug-2026
Closing Date
03-Sep-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.
What AstraZeneca employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom