Clinical Research Associate Job at AstraZeneca, USA | Life Sciences Candidates, Apply Now & Earn Upto $168,231

Clinical Research Associate Job at AstraZeneca, USA | Life Sciences | Earn Upto $168,231

If you are an experienced clinical operations professional, a specialized field monitor, or an analytical life scientist looking to anchor your career with a premier global biopharmaceutical leader, this full-time role at AstraZeneca is an exceptional opportunity. Strategically located within either Ohio or Michigan, this field-based position places you on the frontline of clinical trial delivery and localized data integrity. For detail-oriented monitoring experts searching for a high-impact Clinical Research Associate Job, this position offers total operational ownership over Risk-Based Quality Management (RbQM), electronic Trial Master File (eTMF) curation, and full site-lifecycle governance. It serves as an elite launchpad to advance a long-term AstraZeneca career and stands out as a premier choice for anyone tracking a competitive Life Sciences Job within a world-class therapeutic development network.

About The Company

AstraZeneca is a global, science-led biopharmaceutical powerhouse focused on the discovery, development, and commercialization of prescription medicines across multiple therapeutic areas, including Oncology, Rare Diseases, Cardiovascular, Renal, Metabolism, and Respiratory & Immunology. Operating in over 100 countries, AstraZeneca transforms innovative science into life-saving medicines that protect millions of patients worldwide. This position integrates directly into the local US clinical operations division, placing you in either the Ohio or Michigan regional node. Operating within a highly collaborative Local Study Team (LST), you will work in tandem with regional Clinical Trial Associates, Line Managers, and Local Study Managers (LSM). Rather than navigating chaotic multi-vendor variables, you will focus deeply on AstraZeneca’s specific pipeline protocols and proprietary data systems, ensuring that investigational molecules transition smoothly through crucial clinical phases.

Clinical Research Associate Job – Key Responsibilities

The Clinical Research Associate (CRA) assumes local responsibility for the operational preparation, execution, compliance, and clinical data integrity of allocated investigative sites.

Your core site management, document auditing, and milestone verification duties include:

• Site Evaluation & Start-Up: Contributing to the selection of potential investigators and executing Site Qualification Visits (SQV), collection, review, and tracking of documents for the health authority application process.
• ICH-GCP Quality Assurance: Initiating, monitoring, and closing study sites in strict compliance with AstraZeneca Procedural Documents, international ICH-GCP frameworks, and local FDA regulations to advance this Clinical Research Associate Job.
• Comprehensive Monitoring visits: Performing regular monitoring visits (both remote and onsite) alongside routine remote data checks in strict accordance with the study-specific Monitoring Plan.
• Data Verification & Auditing: Executing Source Data Review (SDR), Case Report Form (CRF) audits, and comprehensive Source Data Verification (SDV) to protect data entry quality.
• Risk-Based Quality Management: Applying fundamental Risk-Based Quality Management (RbQM) principles, performing regular Site Quality Risk Assessments, and adapting monitoring intensity dynamically during the study.
• Safety & Deviation Triage: Securing the accurate, timely reporting of Serious Adverse Events (SAEs) and protocol deviations, while escalating systematic compliance or data privacy breaches to Clinical Quality Management (CQM).
• eTMF Architecture Maintenance: Ensuring the timely collection and uploading of essential documents into the electronic Trial Master File (eTMF) to support a prominent Life Sciences Job.
• Supply & Drug Accountability: Managing the chain of custody for investigator site files (ISF), tracking drug supply storage, and preparing investigational medicinal products for witnessed destruction when required.

Qualifications & Profile Requirements For Clinical Research Associate Job

AstraZeneca seeks a systematic, detail-oriented clinical research professional who demonstrates strong negotiation skills and an uncompromising commitment to protocol compliance.

• Required Academic Criteria:
  • Educational Foundation: A completed formal Bachelor’s degree in a related natural science discipline, preferably in the Life Sciences, or an equivalent qualification calibrated to successful clinical trial conduct.
• Essential Knowledge & Experience:
  • Industry Track Record: Direct, independent clinical monitoring experience executed within the pharmaceutical or CRO industry sectors to build an AstraZeneca career.
  • Regulatory Grounding: Excellent working knowledge of international ICH-GCP guidelines, combined with a basic functional understanding of Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP).
  • Clinical Operations Fluency: Strong, practical understanding of clinical study management mechanics, including remote monitoring tools, electronic case report forms, data management, and drug handling.
  • Therapeutic Aptitude: Good medical knowledge and the immediate capability to adapt to specific AstraZeneca therapeutic areas and protocols.
• Soft Skills & Mobility:
  • Excellent attention to detail, strong verbal and written communication traits, and exceptional interpersonal collaboration skills.
  • Mobility Credentials: Possession of a valid domestic driving license, with the complete flexibility to travel nationally or internationally as required by monitoring plans.

Logistics, Compensation & Corporate Employee Perks

• Location Base: Field-Based (Residing in either Ohio or Michigan, United States).
• Employment Status: Salaried / Salaried Non-Exempt Full-Time Position.
• Annual Base Salary Range: $112,154.40 – $168,231.60 USD Annually (Actual starting offers are calibrated based on individualised factors, including local geography, specific therapeutic experience, and monitoring skill level; overtime eligibility applies when working qualifying hours).
• Short & Long-Term Incentives: Eligibility to participate in a short-term incentive bonus opportunity alongside AstraZeneca’s equity-based long-term incentive program.
• Financial Protection: Qualified retirement program [401(k) plan] featuring competitive corporate contribution matching structures.
• Health & Welfare Rewards: Comprehensive health benefits package starting early in your onboarding, including medical, prescription drug, dental, and vision coverage.
• Work-Life Balance Support: Generous paid vacation allocations, observed company holidays, and comprehensive paid leave options.

In short, the regional Clinical Research Associate position at AstraZeneca is a definitive route to transitioning your field monitoring background into a high-visibility global biopharmaceutical asset. Securing an appointment here allows you to bypass transactional multi-CRO workloads and take centralised, strategic charge of the RbQM systems, eTMF metrics, and investigator relationships that advance next-generation therapeutics safely through US clinical pipelines. If you reside in Ohio or Michigan, meet the life sciences degree benchmarks, and possess an uncompromising eye for clinical data integrity, apply today to secure this premier Clinical Research Associate Job, launch an exceptional AstraZeneca career, and lock in this outstanding Life Sciences Job.

APPLY ONLINE HERE