
10,000+ employees
Founded 1999
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
💰 Post-IPO Debt on 2023-02
Biotechnology • Pharmaceuticals • Science
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines. It primarily works in areas of oncology, cardiovascular, renal & metabolism, and respiratory diseases. With operations in over 100 countries, AstraZeneca is dedicated to scientific research and a commitment to providing effective treatments and improving patient health across a wide array of conditions.
🕒 5 days ago
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10,000+ employees
Founded 1999
🧬 Biotechnology
💊 Pharmaceuticals
🔬 Science
💰 Post-IPO Debt on 2023-02
Biotechnology • Pharmaceuticals • Science
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines. It primarily works in areas of oncology, cardiovascular, renal & metabolism, and respiratory diseases. With operations in over 100 countries, AstraZeneca is dedicated to scientific research and a commitment to providing effective treatments and improving patient health across a wide array of conditions.
• Contributes to the selection of potential investigators. • CRAs are accountable for study start-up and regulatory maintenance. • Trains, supports and advises Investigators and site staff in study-related matters, including Risk Based Quality Management (RbQM) principles. • Ensures the sites are inspection ready at all times. • Initiates, monitors and closes study sites in compliance with AZ Procedural Documents. • Manages study supplies and drug accountability at study site. • Performs monitoring visits (remote and onsite). • Works with data management to ensure robust quality of the collected study data. • Ensures accurate and timely reporting of Serious Adverse Events and their follow-ups. • Prepares and finalises monitoring visit reports in CTMS and provides timely feedback to the Principal Investigator.
• Bachelor degree in related discipline, preferably in life science, or equivalent qualification. • Excellent knowledge of international guidelines ICH-GCP, basic knowledge of GMP/GDP. • Good knowledge of relevant local regulations. • Good medical knowledge and ability to learn relevant AZ Therapeutic Areas. • Basic understanding of the drug development process. • Good understanding of Clinical Study Management including monitoring, study drug handling and data management. • Excellent attention to details. • Good written and verbal communication skills. • Good collaboration and interpersonal skills. • Good negotiation skills. • Ability to travel nationally/internationally as required. • Valid G driving license.
• Competitive Flex Benefits & Retirement Savings Program • 4 weeks’ paid vacation • Annual Personal Days • Contract Benefits Program
Apply Now🕒 June 5
Clinical Research Associate at ICON designing and analyzing clinical trials, ensuring protocol compliance and contributing to the advancement of innovative treatments.
🕒 May 27
Clinical Research Associate II responsible for monitoring oncology clinical trials at IQVIA Biotech. Ensuring compliance and managing site activities for clinical studies.
🇨🇦 Canada – Remote
💵 $73.6k - $140k / year
💰 $1G Post-IPO Debt on 2023-05
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🗣️🇫🇷 French Required
🕒 May 5
Legal Research Analyst handling legal research and retrieval tasks for law firm clients. Requires strong research skills using various legal databases and tools.