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Astrazeneca Clinical Research Jobs (NOW HIRING)

AstraZeneca

Senior Scientist - Evinova

Gaithersburg, MD · On-site

$98K - $135K/yr

Evinova draws on AstraZeneca's deep experience developing novel therapeutics, informed by insights from thousands of patients and clinical researchers. Together, we can accelerate the delivery of ...

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Astrazeneca Clinical Research information

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$49K

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$189K

How much do astrazeneca clinical research jobs pay per year?

As of Aug 7, 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 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 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.

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 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.

Is it hard to get a Astrazeneca Clinical Research job?

Securing a Clinical Research position at AstraZeneca typically requires relevant education, such as a degree in life sciences or healthcare, and experience in clinical trials or research. The hiring process can be competitive, often involving multiple interview stages and demonstrating knowledge of Good Clinical Practice (GCP) and regulatory standards.
More about Astrazeneca Clinical Research jobs
What cities are hiring for Astrazeneca Clinical Research jobs? Cities with the most Astrazeneca Clinical Research job openings:
What states have the most Astrazeneca Clinical Research jobs? States with the most job openings for Astrazeneca Clinical Research jobs include:
What job categories do people searching Astrazeneca Clinical Research jobs look for? The top searched job categories for Astrazeneca Clinical Research jobs are:
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, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Associate, Cell Therapy - Texas

AstraZeneca

Wilmington, DE • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

21st of 86 rated pharmaceutical

Job description

The Clinical Research Associate (CRA) has local responsibility for the delivery of studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the primary contact with study sites and is responsible for monitoring study conduct to ensure proper delivery of clinical trials.
This is a field-based position with a strong preference for candidates based in Texas.
The CRA is responsible for the preparation, initiation, monitoring, and closure of assigned sites in clinical studies in compliance with AstraZeneca Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations, ensuring that sites deliver according to study commitments.
A CRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Associate Director (LSAD) role.
Typical Accountabilities
  • Contributes to the selection of potential investigators.

  • Supports study start-up and regulatory maintenance activities, including Site Qualification Visits (SQVs), collection and review of regulatory documents, and submission activities to EC/IRB and Regulatory Authorities as applicable.

  • Trains, supports, and advises investigators and site staff on study-related matters, including Risk Based Quality Management (RbQM) principles.

  • Confirms site staff have completed required training, including ICH-GCP training, prior to and throughout the study duration. Ensures sites remain inspection ready at all times.

  • Actively participates in Local Study Team (LST) meetings.

  • Contributes to Investigator Meetings as applicable.

  • Initiates, monitors, and closes study sites in compliance with AstraZeneca Procedural Documents. Shares updates on patient recruitment and site performance within the LST.

  • Drives site performance by proactively identifying, resolving, and escalating study-related issues as appropriate.

  • Updates CTMS and other clinical systems within required timelines.

  • Manages study supplies, ISF documentation, investigational product accountability, and study drug reconciliation/destruction activities where applicable.

  • Performs onsite and remote monitoring visits, including remote data review activities, in accordance with study-specific Monitoring Plans.

  • Performs Source Data Review (SDR), Source Data Verification (SDV), and CRF review activities.

  • Conducts Site Quality Risk Assessments and adjusts monitoring intensity accordingly throughout the study.

  • Ensures timely resolution of data queries and collaborates with Data Management to maintain high-quality study data.

  • Ensures accurate and timely reporting of Serious Adverse Events (SAEs) and follow-up documentation.

  • Prepares and finalizes monitoring visit reports and follow-up letters within required timelines and in accordance with AstraZeneca SOPs.

  • Follows up on outstanding site actions to ensure timely resolution.

  • Escalates significant quality issues, compliance concerns, data privacy breaches, or ICH-GCP deviations to Local Management and/or Quality teams as required.

  • Assists sites in maintaining inspection-ready Investigator Site Files (ISF).

  • Supports audit and regulatory inspection readiness activities in collaboration with LSAD and Quality teams.

  • Ensures timely collection and upload of essential documents into the eTMF in compliance with ICH-GCP, AstraZeneca SOPs, and local requirements.

  • Ensures study documentation is complete and ready for final archiving activities.

  • Provides insights regarding investigators, sites, and competing studies relevant to the local market.

  • Ensures compliance with AstraZeneca's Code of Ethics and company policies related to Safety, Health & Environment (SHE), security, technology, finance, and people practices.

  • Ensures compliance with local, national, and regional regulations as applicable.

  • Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management.

Minimum Qualifications
  • Bachelor's degree in Life Sciences or related discipline, or equivalent qualification.

  • Minimum 3 years of CRA or similar relevant clinical research experience within the pharmaceutical, biotechnology, or CRO industry.

  • Excellent knowledge of ICH-GCP guidelines and basic knowledge of GMP/GDP.

  • Good knowledge of relevant local regulations and clinical trial requirements.

  • Strong medical and scientific aptitude with the ability to learn AstraZeneca therapeutic areas.

  • Basic understanding of the drug development process.

  • Good understanding of Clinical Study Management, including site monitoring, study drug handling, and data management.

  • Strong attention to detail and documentation accuracy.

  • Excellent written and verbal communication skills.

  • Strong collaboration, interpersonal, and relationship-building skills.

  • Good negotiation and conflict-resolution skills.

  • Ability to travel nationally and internationally as required.

Desirable Qualifications
  • Clinical trial or relevant experience in Cell Therapy preferred. Ability to work effectively in an environment with remote collaborators and cross-functional teams.

  • Positive and adaptable approach to change management.

  • Ability to identify and champion process improvements that increase efficiency and quality.

  • Strong analytical and problem-solving capabilities.

  • Ability to prioritize and manage multiple competing deadlines effectively.

  • Familiarity with risk-based monitoring methodologies, including remote monitoring.

  • Good cultural awareness and ability to work within global teams.

  • Proficiency with clinical systems, software platforms, and technology-enabled environments.

  • Team-oriented, flexible, and responsive to shifting priorities and business needs.

Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
So, what's next?
Are you already imagining yourself joining our team? Good, because we can't wait to hear from you!
The annual base pay for this position ranges from $112,154.40 - $168,231.60. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. 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). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
31-Jul-2026
Closing Date
06-Aug-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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