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- Tasks: Deliver clinical studies, monitor compliance, and support site staff in research activities.
- Company: AstraZeneca is a global biopharmaceutical leader focused on innovative medicines and healthcare solutions.
- Benefits: Enjoy a culture of empowerment, diversity, and opportunities for global career advancement.
- Why this job: Make a meaningful impact in healthcare while growing your skills in a supportive environment.
- Qualifications: Bachelor’s degree in life sciences and 1-2 years of clinical research experience required.
- Other info: Recognised as one of Vietnam’s Top 100 Best Places to Work from 2018 to 2024.
The predicted salary is between 28800 - 43200 £ per year.
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 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.
AstraZeneca Vietnam is a Foreign Invested Enterprise with over 600 members, having 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.
Clinical Research Associate_Biopharm_HCMC employer: AstraZeneca GmbH
Contact Detail:
AstraZeneca GmbH Recruiting Team
recruitment.Vietnam@astrazeneca.com
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate_Biopharm_HCMC
✨Tip Number 1
Familiarise yourself with AstraZeneca's core values and recent projects in the biopharmaceutical field. This knowledge will help you demonstrate your alignment with their mission during interviews.
✨Tip Number 2
Network with current or former Clinical Research Associates at AstraZeneca through LinkedIn. They can provide valuable insights into the company culture and expectations, which can be beneficial for your application.
✨Tip Number 3
Stay updated on the latest trends in clinical research and drug development. Being knowledgeable about ICH-GCP guidelines and local regulations will show your commitment to the role and industry.
✨Tip Number 4
Prepare specific examples from your past experience that highlight your attention to detail and problem-solving skills. These anecdotes will help you stand out during interviews and showcase your suitability for the CRA position.
We think you need these skills to ace Clinical Research Associate_Biopharm_HCMC
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a Clinical Research Associate at AstraZeneca. Familiarise yourself with the key tasks mentioned in the job description, such as monitoring study conduct and ensuring compliance with regulations.
Tailor Your CV: Customise your CV to highlight relevant experience in clinical research. Emphasise your knowledge of ICH-GCP guidelines and any previous roles that demonstrate your attention to detail and ability to collaborate effectively.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the biopharmaceutical industry. Mention specific experiences that align with AstraZeneca's values and how you can contribute to their mission of improving healthcare.
Proofread Your Application: Before submitting your application, carefully proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial for a Clinical Research Associate.
How to prepare for a job interview at AstraZeneca GmbH
✨Know Your ICH-GCP Guidelines
Familiarise yourself with the International Council for Harmonisation Good Clinical Practice (ICH-GCP) guidelines. Being able to discuss these in detail will show your understanding of clinical research standards and your commitment to compliance.
✨Demonstrate Attention to Detail
As a Clinical Research Associate, attention to detail is crucial. Prepare examples from your past experiences where your meticulous nature led to successful outcomes, especially in data management or study execution.
✨Showcase Your Teamwork Skills
AstraZeneca values collaboration. Be ready to share instances where you worked effectively within a team, highlighting your communication and negotiation skills, as well as how you supported others in achieving common goals.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities and adaptability. Think about challenges you've faced in previous roles and how you managed them, particularly in a clinical research context.
