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AstraZeneca

Senior Clinical Research Associate – East Coast

AstraZeneca

. Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP) .

Posted 4/22/2026full-timeAtlanta • Florida • 🇺🇸 United StatesSeniorWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Performing selection, initiation, interim monitoring and closeout visits (remote and onsite), as well as remote data checks, in accordance with the timelines specified in the study specific Clinical Monitoring Plan (CMP)
  • Driving performance at the sites
  • Proactively identifying and ensuring timely resolution to study-related issues and escalate them as appropriate
  • Training, supporting and advising Investigators and site staff in study related matters, including Risk Based Quality Management (RBQM) principles
  • Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones
  • Document recruitment barriers and mitigation plans
  • Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator, including follow-up letter, within required timelines and in line with Alexion SOPs
  • Ensuring timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Alexion SOPs and local requirements

Requirements

What you’ll need
  • Minimum of 4 years of CRA monitoring experience
  • Bachelors degree in related discipline, preferably in life science, or equivalent qualification
  • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP
  • Excellent knowledge of relevant local regulations
  • Good medical knowledge and ability to learn relevant Alexion Therapeutic Areas
  • Good understanding of the drug development process
  • Excellent understanding of Clinical Study Management including monitoring, study drug handling and data management
  • Excellent attention to detail
  • Excellent written and verbal communication skills
  • Excellent collaboration and interpersonal skills
  • Good negotiation skills
  • Valid driving license

Benefits

Comp & perks
  • Health insurance
  • Competitive salary
  • Paid time off

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
CRA monitoring experienceClinical Monitoring Plan (CMP)Risk Based Quality Management (RBQM)monitoring visit reportseTMFICH-GCPGMPGDPClinical Study Managementdata management
Soft Skills
attention to detailwritten communicationverbal communicationcollaborationinterpersonal skillsnegotiation skills