AstraZeneca

Clinical Research Associate, Oncology

AstraZeneca$101K — $152K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required, preferably in Life Sciences.
  • Minimum 2 years CRA or Study Coordinator experience in Oncology.
  • Fluent in spoken and written English.
  • Strong understanding of ICH/GCP guidelines and basic GMP/GDP knowledge.
  • Familiar with local regulations related to clinical studies.
  • Good medical knowledge in relevant AZ Therapeutic Areas.
  • Basic understanding of the drug development process.

Responsibilities

  • Manage the delivery of studies at assigned centers.
  • Collaborate with local teams to ensure study quality and timelines are met.
  • Prepare, initiate, monitor, and close clinical trial centers as per guidelines.
  • Ensure compliance with AZ Procedural Documents and international regulations.
  • Deliver according to trial commitments, maintaining high standards.

Benefits

  • 401(k) qualified retirement program.
  • Paid vacation and holidays.
  • Health benefits including medical, dental, and vision coverage.
  • Paid leaves available.
  • Short-term incentive bonus opportunity.
Full Job Description
Clinical Research Associate (CRA), Oncology,

As a Field Based Clinical Research Associate, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives.

In this role as an Oncology CRA, you will have the local responsibility for the delivery of the studies at allocated centers and are active participants in the local study team(s). You'll work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner.

You will also be responsible for the preparation, initiation, monitoring and closure of an agreed number of centers in clinical studies according to AZ Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations. Deliver according to the commitment in the individual trials.

Minimum Requirements:
  • Bachelor's degree required, preferably in Life Science field
  • Minimum 2 years of CRA experience or Study Coordinator in Oncology therapeutic experience required
  • Fluent knowledge of spoken and written English
  • Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
  • Good knowledge of relevant local regulations
  • Good medical knowledge in 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
  • Ability to travel as required, 50-70%


Competencies and Skills:
  • Ability to deliver quality according to the requested standards
  • Ability to work in an environment of remote collaborators
  • Manages change with a positive approach for self, team, and the business. Sees change as an opportunity to improve performance and add value to the business
  • Ability to look for and champion more efficient and effective methods/processes of delivering quality clinical trials with a reduced budget and in less time
  • Excellent written and verbal communication skills, negotiation, collaboration, and interpersonal skills
  • Good analytical and problem-solving skills
  • Demonstrates ability to prioritize and manage multiple tasks with conflicting deadlines
  • Good cultural awareness
  • Ability to understand the impact of technology on projects and to use and develop computer skills while making appropriate use of systems/software in an e-enabled environment
  • Team-oriented and flexible; ability to respond quickly to shifting demands and opportunities


The annual base salary (or hourly rate of compensation) for this position ranges from $ 101,948.00 - 152,922.00. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Date Posted
07-Apr-2026

Closing Date
29-Apr-2026

About AstraZeneca

AstraZeneca is a British-Swedish multinational pharmaceutical company that specializes in the research, development, and manufacturing of prescription drugs. The company was formed in 1999 through the merger of Astra AB and Zeneca Group plc. AstraZeneca's products are used to treat a wide range of medical conditions, including cancer, cardiovascular disease, respiratory disease, and diabetes. The company has operations in over 100 countries and employs more than 76,000 people worldwide. AstraZeneca is committed to developing innovative medicines that improve the health and well-being of people around the world.
Learn more about AstraZeneca
Size
83,100 employees
Market Cap
$211.5 billion
Industry
Net Income
$3.1 billion
Founded
1999
5 Year Trend
+10.2%
Revenue
$26.6 billion
NASDAQ

Similar Jobs

More Jobs at AstraZeneca

More Pharmaceuticals & Biotech Jobs

Find similar Clinical Research Associate, Oncology jobs: