Clinical Research Associate_Biopharm_HCMC

Clinical Research Associate – Biopharm – HCM The ideal candidate is a passionate, self-motivated, and detail-oriented team player committed to our customers\’ success. If this describes you, AstraZeneca might be the right place for you! About AstraZeneca and AstraZeneca Vietnam AstraZeneca AstraZeneca (LSE/STO/Nasdaq: AZN) is a global, science-led biopharmaceutical company focused on discovering, developing, and commercializing medicines in Oncology, Rare Diseases, and BioPharmaceuticals, including Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Based in Cambridge, UK, AstraZeneca operates in over 100 countries, with medicines used by millions worldwide. Visit astrazeneca.com and follow @AstraZeneca on Twitter. AstraZeneca Vietnam As a Foreign Invested Enterprise with over 600 members, AstraZeneca has invested 360 million USD in Vietnam from 2020 to 2030, focusing on reducing non-communicable diseases, developing local talent, and enhancing R&D and manufacturing capabilities. Over the past three decades, AstraZeneca has collaborated with the Vietnamese government and healthcare partners on disease awareness, prevention, and early detection programs. The company has received multiple awards for its contributions to healthcare and has been recognized as one of Vietnam’s Top 100 Best Places to Work (2018–2024). What you’ll do The Clinical Research Associate (CRA) is responsible for delivering clinical studies at assigned sites and participating in local study teams. The CRA collaborates closely with other CRAs and the Study Team to ensure timely and efficient study execution. The CRA acts as the main contact at study sites and monitors study conduct to ensure compliance and quality. The CRA manages the preparation, initiation, monitoring, and closure of sites, ensuring adherence to AstraZeneca procedures, ICH-GCP guidelines, and local regulations. Longer-tenure CRAs may take on additional responsibilities, including Local Study Manager tasks. Key responsibilities include: Assisting in investigator selection and study start-up activities, including regulatory submissions and documentation. Training and supporting investigators and site staff in study procedures and quality standards. Participating in study meetings and monitoring visits (remote and onsite). Managing study supplies, drug accountability, and data entry in CTMS. Performing data review, source verification, and risk assessments. Ensuring timely reporting of adverse events and study documentation. Preparing for audits and inspections. Maintaining compliance with company policies, ethics, and local laws. Education, Qualifications, Skills, and Experience Essential: Bachelor’s degree in life sciences or related field. 1-2 years of clinical research experience. Knowledge of ICH-GCP, GMP/GDP, and local regulations. Good medical knowledge and understanding of drug development and clinical trial management. Strong attention to detail, communication, collaboration, and negotiation skills. Willingness to travel as needed. Desirable: Experience working remotely and managing change. Ability to optimize processes, analyze problems, and prioritize tasks. Familiarity with risk-based monitoring and digital tools. Cultural awareness and adaptability. Why AstraZeneca? Join us to make a meaningful impact, grow professionally, and help bring innovative medicines to patients worldwide. We foster a culture of empowerment, diversity, and continuous learning, offering opportunities to advance your career globally. Next steps If you’re inspired to join our team, we look forward to your application. For more information, contact recruitment.Vietnam@astrazeneca.com . Learn more Visit our website , follow us on LinkedIn , or contact us via email. #J-18808-Ljbffr