Search by job, company or skills

AstraZeneca

Clinical Research Associate (CRA) Graduate Programme (1 year period)

Fresher
Save
new job description bg glownew job description bg glownew job description bg svg
  • Posted 3 hours ago
  • Be among the first 10 applicants
Early Applicant

Job Description

About Clinical Research at AstraZeneca

AstraZeneca's vision in Oncology Research & Development (R&D) is to push the boundaries of science to change the practice of medicine, transform the lives of patients living with cancer, and ultimately eliminate cancer as a cause of death. Our broad pipeline of next-generation oncology medicines has nearly 100 clinical trials ongoing. The Site Management and Monitoring (SMM) organization is responsible for delivering cost-effective and high-quality study data to Oncology R&D. We work across approximately 40 countries, managing and monitoring activities focused on protecting patients, supporting investigators, and ensuring reliable data is delivered. Our scope includes phase I-IV studies at global, local, and regional levels. We focus on internally-led studies supporting various Therapeutic Areas including lung, breast, gastrointestinal, genitourinary, and hematology.

About the Programme

Our program provides a springboard to your future career as a Clinical Research Associate (CRA). Our Graduate Programme offers opportunities throughout the 1-year program to make real contributions and work on projects supporting teams in three placements including Trial Master File Administration, Study Start-Up, and Site Monitoring. Supported by experts in their field, you will receive mentoring and training to expand your knowledge and prepare you for a career as an Oncology CRA.

What you can expect

  • An assigned mentor throughout the program, dedicated training, and opportunities to learn the AstraZeneca way.
  • Activities and training designed to build your oncology knowledge and expertise.
  • A highly supportive and collaborative environment with opportunities to connect with internal and external oncology SMM stakeholders, building your clinical research network.
  • Continuous opportunities to hone your communication and critical thinking skills.

What you will be doing

Our program is designed to help you understand the way we work support the overall delivery of the oncology portfolio and provide insights into the collaborative, cross-functional CRA role. Through the placements, you will develop skills in building and maintaining multi-disciplinary relationships. Over the course of the program, you will receive mentoring and feedback from managers and colleagues, so you'll be able to identify areas of strength, as well as those you want to further develop.

Placement 1: Trial Master File Administration

You will learn and become an expert on the essential documents required to support a site's electronic Trial Master File (eTMF). You will collect, quality-check and file regulatory documents from oncology institutions that support the delivery of the study.

Placement 2: Study Start-Up

You will join the internal Study Start-Up (SSU) team, working to quickly and efficiently support a site through to activation.

Placement 3: Site Monitoring

You will be undergoing a series of trainings including oncology-focused modules and mock visit opportunities, all to learn how to be a successful oncology monitor. There will also be opportunities to attend and observe a monitoring visit with an experienced oncology monitor.

Post-Programme:

Upon completion of the program, there is an opportunity for a full-time CRA position based on participant interest, performance, and business needs.

To be eligible for the program, you'll need:

  • Bachelor's degree in a related discipline, preferably in life sciences, or equivalent.
  • Welcome fresh graduate of pharmacy.
  • Strong interest in clinical research as a career.
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines.
  • Good attention to detail and critical-thinking skills
  • Good written and verbal communication skills (English and Thai)
  • Strong organizational, interpersonal, and collaboration skills.
  • A passion for working in pharmaceuticals, with a real desire to make a difference to patients.
  • Team-oriented and flexible; ability to respond quickly to shifting demands and opportunities.
  • Ability to travel nationally as required.
  • Excellent in Thai and English languages in both communication and written
  • Team: Site Management & Monitoring Thailand
  • Location: Bangkok, Thailand.

Application Period: 9 April to 3 May 2026.

Interview Period: 13 May to 15 May 2026

On-Boarding Period: 1 June 2026

Why AstraZeneca

At AstraZeneca, we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference in medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and is always committed to lifelong learning, growth, and development. We're on an exciting journey to pioneer the future of healthcare.

Find out more

Our social media, Follow AstraZeneca on LinkedIn

Follow AstraZeneca on Facebook

Follow AstraZeneca on Instagram

More Info

Job Type:
Industry:
Employment Type:

About Company

Job ID: 146591641