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Astrazeneca Clinical Research information

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$49K

$107.3K

$189K

How much do astrazeneca clinical research jobs pay per year?

As of Aug 28, 2026, the average yearly pay for astrazeneca clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is AstraZeneca clinical research?

AstraZeneca Clinical Research refers to the scientific studies and trials conducted by AstraZeneca, a global pharmaceutical company, to evaluate the safety and effectiveness of new drugs and treatments in humans. These clinical research programs are essential for developing innovative medicines and ensuring they meet regulatory standards before becoming available to patients. The process typically involves multiple phases, starting with small-scale trials and progressing to larger, more comprehensive studies. AstraZeneca collaborates with healthcare professionals, research institutions, and regulatory agencies throughout the research process. This work helps advance medical knowledge and brings new therapies to market.

What are the key skills and qualifications needed to thrive in clinical research at AstraZeneca?

To thrive in Clinical Research at AstraZeneca, you need a solid background in life sciences, clinical trial processes, and regulatory compliance, usually supported by a relevant degree and experience in clinical research. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications such as GCP (Good Clinical Practice) are commonly required. Strong analytical thinking, attention to detail, and effective communication enable you to manage complex studies and collaborate with cross-functional teams. These skills are crucial for ensuring high-quality research outcomes, regulatory adherence, and successful new drug development.

What are some common challenges faced by clinical research professionals at AstraZeneca, and how can they be addressed?

Clinical Research professionals at AstraZeneca often navigate complex regulatory requirements, tight project timelines, and the need for cross-functional collaboration with global teams. Managing multiple stakeholders and adapting to evolving study protocols are frequent challenges. To address these, AstraZeneca provides structured onboarding, robust training, and encourages open communication within multidisciplinary teams, ensuring that employees have the support and resources needed to overcome obstacles and deliver high-quality research outcomes.

What is the difference between Astrazeneca Clinical Research vs Astrazeneca Medical Affairs?

AspectAstrazeneca Clinical ResearchAstrazeneca Medical Affairs
Primary FocusDesigning and managing clinical trials to evaluate drug safety and efficacyProviding scientific and medical support to healthcare professionals and internal teams
Required CredentialsTypically requires a degree in life sciences, nursing, or pharmacy; clinical research certifications are commonRequires a medical degree or advanced scientific qualification; medical licensing may be preferred
Work EnvironmentClinical trial sites, research labs, or officesCorporate offices, medical communication settings, or healthcare conferences
Industry UsageUsed in pharmaceutical companies, CROs, and research institutionsUsed within pharmaceutical companies' medical or scientific departments

In summary, Astrazeneca Clinical Research focuses on conducting and managing clinical trials, while Astrazeneca Medical Affairs provides scientific support and medical communication. Both roles require scientific credentials but differ in daily tasks and work environments.

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Astrazeneca Clinical Research jobs near you
Infographic showing various Astrazeneca Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research & Development Director

Waltham, MA • On-site

AstraZeneca
Pharmaceutical Product Wholesalers • 10K+ employees

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

People enjoy working here

Good employer

Recommended by students

Learn more about AstraZenecaexternal

Full-time

Posted 16 days ago

Job description

What You Will Do
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.
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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

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