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 ...
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 ...
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 ...
Sr. Process Development Engineer - OSD
$140K - $154K/yr
You will operate within cross functional teams to ensure alignment during drug product development, join the CMC teams, and provide leadership for development teams. You will design and execute ...
Sr. Process Development Engineer - OSD
$140K - $154K/yr
You will operate within cross functional teams to ensure alignment during drug product development, join the CMC teams, and provide leadership for development teams. You will design and execute ...
Sr. Process Development Engineer - OSD
Waltham, MA · On-site
$140K - $154K/yr
You will operate within cross functional teams to ensure alignment during drug product development, join the CMC teams, and provide leadership for development teams. You will design and execute ...
Sr. Process Development Engineer - OSD
Waltham, MA · On-site
$140K - $154K/yr
You will operate within cross functional teams to ensure alignment during drug product development, join the CMC teams, and provide leadership for development teams. You will design and execute ...
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 ...
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 ...
Director, Drug Safety & Pharmacovigilance Scientist
Waltham, MA · On-site
$220 - $240/hr
The Director collaborates across Clinical Development, Clinical Operations, Regulatory Affairs ... Drug Safety & Pharmacovigilance and the broader organization. Pharmacovigilance Operations ...
Director, Drug Safety & Pharmacovigilance Scientist
Waltham, MA · On-site
$220 - $240/hr
The Director collaborates across Clinical Development, Clinical Operations, Regulatory Affairs ... Drug Safety & Pharmacovigilance and the broader organization. Pharmacovigilance Operations ...
Director, Program Management
Waltham, MA · On-site
A successful candidate must have experience managing drug development projects in a fast-paced environment, with a strong willingness to build relationships with cross-functional teams, dive into ...
Director, Program Management
Waltham, MA · On-site
A successful candidate must have experience managing drug development projects in a fast-paced environment, with a strong willingness to build relationships with cross-functional teams, dive into ...
Research Associate - RNA Synthesis Platform Development
Waltham, MA · On-site
$65 - $93/hr
In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions. About ... Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms ...
New
Research Associate - RNA Synthesis Platform Development
Waltham, MA · On-site
$65 - $93/hr
In R&D, you'll drive breakthroughs that could turn the impossible into possible for millions. About ... Work at the forefront of drug discovery, harnessing cutting‑edge AI, data, and digital platforms ...
New
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 ...
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 research ...
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 research ...
Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT)
Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT)
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159 - $195/hr
Associate Director, Formulation and Drug Product Development Apply for this job Department: 1110GL - Technical Development Location: Waltham, MA Company Overview: Dyne Therapeutics is focused on ...
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159 - $195/hr
Associate Director, Formulation and Drug Product Development Apply for this job Department: 1110GL - Technical Development Location: Waltham, MA Company Overview: Dyne Therapeutics is focused on ...
Production Automation Lead
Waltham, MA · On-site
$120 - $160/hr
Dash accelerates drug development. By fusing advanced automation-native lab workflows and integrated software into a unified platform, we provide the biopharma industry with the high-velocity, high ...
Production Automation Lead
Waltham, MA · On-site
$120 - $160/hr
Dash accelerates drug development. By fusing advanced automation-native lab workflows and integrated software into a unified platform, we provide the biopharma industry with the high-velocity, high ...
Demonstrated deep knowledge of the integrated drug development process * Demonstrated ability to find solutions and alternatives through teamwork resulting in positive business outcomes
Demonstrated deep knowledge of the integrated drug development process * Demonstrated ability to find solutions and alternatives through teamwork resulting in positive business outcomes
The Hematology Research and Development (R&D) team is accountable for all drug development activities in hematology research from first-in-man studies, all the way to late-stage trials leading to ...
The Hematology Research and Development (R&D) team is accountable for all drug development activities in hematology research from first-in-man studies, all the way to late-stage trials leading to ...
Qualifications Drug Safety Specialist needs 5-7 years in Cognos report development and project management, preferably within the pharmaceutical industry. Drug Safety Specialist requires:
Qualifications Drug Safety Specialist needs 5-7 years in Cognos report development and project management, preferably within the pharmaceutical industry. Drug Safety Specialist requires:
Accountabilities Integrate the research, clinical, scientific and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of ...
Accountabilities Integrate the research, clinical, scientific and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of ...
Drug Development information
See Worcester, MA salary details
$32.9K - $42K
2% of jobs
$42K - $51.1K
8% of jobs
$58K is the 25th percentile. Wages below this are outliers.
$51.1K - $60.1K
19% of jobs
$60.1K - $69.2K
20% of jobs
The median wage is $69.5K / yr.
$69.2K - $78.3K
16% of jobs
$85.3K is the 75th percentile. Wages above this are outliers.
$78.3K - $87.4K
13% of jobs
$87.4K - $96.4K
5% of jobs
$96.4K - $105.5K
11% of jobs
$105.5K - $114.6K
2% of jobs
$114.6K - $123.6K
2% of jobs
$123.6K - $132.7K
2% of jobs
$32.9K
$77.3K
$132.7K
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 Worcester, MA?
For Drug Development jobs in Worcester, MA, the most frequently searched job titles are:
What job categories do people searching Drug Development jobs in Worcester, MA look for?
The top searched job categories for Drug Development jobs in Worcester, MA are:
What cities near Worcester, MA are hiring for Drug Development jobs?
Cities near Worcester, MA with the most Drug Development job openings:

AstraZeneca rating
8.4
Based on 45 frontline employees who took The Breakroom Quiz
23rd 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
25-Aug-2026
Closing Date
10-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
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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