Lead project management of cross functional drug development teams andensuredelivery of strategic objectives * Createa shared sense of purpose, inspiring andenergisingothers to build andmaintaina ...
Lead project management of cross functional drug development teams andensuredelivery of strategic objectives * Createa shared sense of purpose, inspiring andenergisingothers to build andmaintaina ...
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 ...
Lead project management of cross functional drug development teams andensuredelivery of strategic objectives * Createa shared sense of purpose, inspiring andenergisingothers to build andmaintaina ...
Lead project management of cross functional drug development teams andensuredelivery of strategic objectives * Createa shared sense of purpose, inspiring andenergisingothers to build andmaintaina ...
Director Clinical Development
Gaithersburg, MD · On-site
$87K - $118K/yr
At least 3 years of relevant experience in clinical drug development across academia or pharmaceutical industry (must include experience conducting early phase trials) * 2 years or more experience as ...
New
Director Clinical Development
Gaithersburg, MD · On-site
$87K - $118K/yr
At least 3 years of relevant experience in clinical drug development across academia or pharmaceutical industry (must include experience conducting early phase trials) * 2 years or more experience as ...
New
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 ...
Lead development of drug project, cross-project, or portfolio strategies * Where applicable, work with alliance partners and run joint alliance forums and governance committee * Identify key business ...
Lead development of drug project, cross-project, or portfolio strategies * Where applicable, work with alliance partners and run joint alliance forums and governance committee * Identify key business ...
Extensive experience leading drug development projects including success in multiple roles/development phases/TAs related to drug development project or program management. Track-record of expertly ...
Extensive experience leading drug development projects including success in multiple roles/development phases/TAs related to drug development project or program management. Track-record of expertly ...
Increased numbers of novel therapeutic agents and the progressively greater complexity of early-phase clinical trials have led to a need for more physicians with special skills in drug development.
Increased numbers of novel therapeutic agents and the progressively greater complexity of early-phase clinical trials have led to a need for more physicians with special skills in drug development.
Strong knowledge of Biometrics standards and workflows (e.g., biostatistics, statistical programming, and clinical data management) in drug development. * Comfort interfacing with IT and enterprise ...
Strong knowledge of Biometrics standards and workflows (e.g., biostatistics, statistical programming, and clinical data management) in drug development. * Comfort interfacing with IT and enterprise ...
The Hematology Research and Early Development (R&D) team has the accountability for all drug development activities in hematology research from first in man studies, all the way to late-stage trials ...
The Hematology Research and Early Development (R&D) team has the accountability for all drug development activities in hematology research from first in man studies, all the way to late-stage trials ...
Senior Manager/Manager, Regulatory Affairs
Germantown, MD · On-site
$110K - $130K/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
Senior Manager/Manager, Regulatory Affairs
Germantown, MD · On-site
$110K - $130K/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 ...
Senior Manager/Manager, Regulatory Affairs
Germantown, MD · On-site
$110K - $130K/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 ...
Senior Manager/Manager, Regulatory Affairs
Germantown, MD · On-site
$110K - $130K/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 ...
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
Quick apply
Generic drug development and approval * Strategic API stockpiling initiatives * Domestic manufacturing expansion and reshoring efforts * Manufacturing technology modernization * Supply chain ...
You will have the opportunity to play an integral role helping our clients and the industry shape the future of drug development * You will be part of an exciting new chapter in Cytel's history with ...
You will have the opportunity to play an integral role helping our clients and the industry shape the future of drug development * You will be part of an exciting new chapter in Cytel's history with ...
S & P Specialist
Bethesda, MD · Hybrid
Knowledge of GCP and ICH guidelines preferred; drug development/clinical trial experience essential. Knowledge of safety databases and/or MedDRA coding preferred Experience leading clinical and cross ...
S & P Specialist
Bethesda, MD · Hybrid
Knowledge of GCP and ICH guidelines preferred; drug development/clinical trial experience essential. Knowledge of safety databases and/or MedDRA coding preferred Experience leading clinical and cross ...
With one of the industry's most diverse and successful portfolios spanning multiple therapeutic areas and modalities, we offer a unique opportunity to contribute to drug development from early ...
With one of the industry's most diverse and successful portfolios spanning multiple therapeutic areas and modalities, we offer a unique opportunity to contribute to drug development from early ...
With one of the industry's most diverse and successful portfolios spanning multiple therapeutic areas and modalities, we offer a unique opportunity to contribute to drug development from early ...
With one of the industry's most diverse and successful portfolios spanning multiple therapeutic areas and modalities, we offer a unique opportunity to contribute to drug development from early ...
Director, Program Management, Late-Stage Development
Gaithersburg, MD · On-site
$157K - $245K/yr
Extensive late-stage R&D drug development knowledge. * Proficiency with MS Project/Smartsheet and PM tools/processes. * Strong cross-functional leadership, stakeholder management, communication, and ...
Director, Program Management, Late-Stage Development
Gaithersburg, MD · On-site
$157K - $245K/yr
Extensive late-stage R&D drug development knowledge. * Proficiency with MS Project/Smartsheet and PM tools/processes. * Strong cross-functional leadership, stakeholder management, communication, and ...
Drug Development information
See Washington 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 is drug development?
What are the typical stages of collaboration between different teams in a drug development role?
What are the key skills and qualifications needed to thrive in drug development, and why are they important?
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.
How much do drug development professionals make?
Is drug development a good career?
What career develops drugs?
What are popular job titles related to Drug Development jobs in Washington?
For Drug Development jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Drug Development jobs in Washington look for?
The top searched job categories for Drug Development jobs in Washington are:
What cities in Washington are hiring for Drug Development jobs?
Cities in Washington with the most Drug Development job openings:

Senior Director, Global Project Management, Cell Therapy
Gaithersburg, MD • Hybrid
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 24 days ago
AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
Job description
Senior Director, Global Project Management, Cell Therapy
Gaithersburg, MD, candidates from Boston, MA will also be considered
Global Portfolio & Project Management (GPPM)
Hybrid Work- on average 3 days/week in office
The Senior Director, Global Project Management, Cell Therapy is a key leadership position,accountable for theprojectmanagementofGlobal Project Teams (GPTs), working alongsideGlobalProduct, Scientific, ClinicalCommercialLeaderstoestablishthe brand strategy and deliverthe approved project plans.
You will be assigned to leadprogrammesof the highest complexity and priority and are regarded as key leaders within theGPT andGPPM organization.This is a critical and exciting opportunity to use your scientific knowledge and strategicexpertiseto lead and influence decisions that will have a direct impact on patients' lives. Working at the highest levels, you will ensure the decisions we make position AstraZeneca for maximum return on investment and positive patient outcomes.
What you'll do
StrategicBusiness Partnership
Provide program management leadership and excellence through active input into the project strategy ensuring alignment of the programstrategy with operational reality
Leaddevelopment of drug project, cross-project, or portfolio strategies
Where applicable, work with alliance partners and run joint alliance forums and governance committee
Identifykey business opportunities orneedsfor strategic shifts based on external and internal events
Partner with Business Development to provide strategic input to potential deal cases (investment & divestment)
Ensureappropriate linkagesbetween project strategy and key internal processes (TA strategy, TA prioritization, corporate scorecard)
Cross-functional Team Leadership and Delivery
Lead project management of cross functional drug development teams andensuredelivery of strategic objectives
Createa shared sense of purpose, inspiring andenergisingothers to build andmaintaina cohesive High Performing Team.
Coach project teamsandGPT towards successful issue resolution and decision making.Engage with critical stakeholders to address barriers or challenges facing team
Focusthe GPT on the right activities at the right time. Coordinate the efforts of sub-teams to ensure delivery at multiple levels of the development team.
Design, implement, andoptimizeeffective communication within and outside the team. Coordinate with corporate communicationstolead the team's external communication plan.
Ensurethe team hasa good informationmanagement system in line with AZ best practice.Ensure integrity of information management systems to connect to external parties. Drive continuous improvement in how the team approaches information management
Ensuredata quality as per agreed standards and monitoring metrics
Identifydevelopment opportunities for team members
Governance and Investment Decisions
Lead team towards optimized governance decisions -e.g.evaluate multiple strategic options and drive team to value-maximizing drug development decisions
Provide guidance to both the team and senior management / governance bodies that allows efficient (timelyand informed) decision making
Leverage broad influential network and ensures engagement at all levels prior to key decisions
Planning, Monitoring and Delivery
Ensure that overall GPT deliverables, budgets, schedules, and performance standards are realistically set, governance approved andattained, and that the project effectively fulfils all information management and business reporting requirements
Direct project support staff inmaintainingplans of the highest data quality, accountable for all integrated project management deliverables associated with the GPT
Accountable for all integrated Project Management deliverables associated with the program
Entrepreneurship
Serve as a role model for cross-functional collaboration and effective conflict resolution
Lead by example in learning and innovation,seek opportunities to change paradigms and remove barriers within and outside the team
Applyextensive business insight to drive cross project learning,championand embed better ways of working across the enterprise.
Proactivelypromotelearning and knowledge sharing. Expected to mentor or supervise other project managers. May provide input for staff development, recruitment, successionplanningand resource model.Helpestablishnew company best practices
Share lessons learned and communicate those throughout the GPM community to drive adoption of knowledge beyond the GPT
Essential for the role
Bachelor's degree in a scientific or business related field
Minimum of 10 years of relevant experience with cross-functional drug development teams.
Extensive experience leading drug development projects including success in multiple roles/development phases/TAs related to drug development project or program management.
Track-record of expertly navigating governance processes to drive complex projects forward.
Successful track record of delivering complex/ high strategic business impact projects within agreed time, quality and cost. Expert knowledge of project management tools and processes.
Experience of driving cross portfolio, above-asset DA or TA drug development projects.
Experience in developing Business Development business cases including pressure testing of proposed timelines, and where applicable, Due Diligence activities.
Skilled at building, motivating, leading and inspiring high performing teams. Proven ability to develop and educate team members and mentor individuals within and outside own function.
Experience in project control, project reporting and ensuring high quality project data (milestone, cost, risk) in enterprise systems.
Track record of effective senior stakeholder management, demonstrating effective communication skills and strong ability to influence strategically using data.
Desirable for the role
Late stage drug development experience
Relevant therapeutic area expertise - CVRM and/or Respiratory & Immunology, and/or cell therapy experience.
Strong internal network with experience in AZ ways of working.
Track-record of building diverse, inclusive teams and delivering in multi-cultural environments.
Office Working Requirements
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.
The annual base pay for this position ranges from $206,993.60 - 310,490.40 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.
Ready to make a difference? Apply now and join us on this exciting journey.
#LI-Hybrid
Date Posted
27-Aug-2026Closing Date
09-Sept-2026Our 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
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About AstraZeneca
Sourced by ZipRecruiter
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. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.
Industry
Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Cambridge, Cambridgeshire, GB