Clinical Research Associate, Oncology

Are you passionate about making a difference in the fight against cancer? Do you thrive in a fast-paced and dynamic environment? If so, we have an exciting opportunity for you! AstraZeneca is seeking a highly motivated and detail-oriented Clinical Research Associate to join our Oncology team. In this role, you will play a critical role in the development of life-saving therapies and treatments for patients with cancer. We are looking for someone with a strong background in oncology research and a keen attention to detail. If you are dedicated to improving patient outcomes and have a passion for advancing scientific research, we want to hear from you. Join us in our mission to make a meaningful impact in the lives of cancer patients worldwide.

1. Conduct clinical trials: The primary responsibility of the Clinical Research Associate (CRA) will be to conduct clinical trials for oncology treatments. This includes coordinating with study sites, monitoring patient progress, and ensuring compliance with study protocols.
2. Data collection and analysis: The CRA will be responsible for collecting and analyzing data from clinical trials, including patient demographics, treatment outcomes, and adverse events. They will also be responsible for maintaining accurate and organized records of all data collected.
3. Compliance with regulations: The CRA will be responsible for ensuring that all clinical trials are conducted in compliance with applicable regulations and guidelines, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
4. Communication with study sites and investigators: The CRA will be responsible for maintaining strong relationships with study sites and investigators, providing support and guidance as needed, and ensuring timely and accurate communication throughout the duration of the clinical trials.
5. Quality control: The CRA will be responsible for performing quality control checks on all study data and ensuring the accuracy and completeness of all study documentation.
6. Collaborate with cross-functional teams: The CRA will work closely with cross-functional teams, including medical affairs, regulatory affairs, and biostatistics, to ensure the successful execution of clinical trials and the development of new treatments.
7. Identify and resolve issues: The CRA will be responsible for identifying any issues or challenges that arise during clinical trials and working with the appropriate teams to resolve them in a timely and efficient manner.
8. Stay updated on industry trends: The CRA will be responsible for staying informed about the latest developments and trends in oncology research and incorporating this knowledge into their work.
9. Travel to study sites: The CRA may be required to travel to study sites to conduct site visits, monitor patient progress, and ensure compliance with study protocols.
10. Uphold ethical standards: The CRA will be responsible for upholding ethical standards in the conduct of all clinical trials, ensuring the safety and

According to JobzMall, the average salary range for a Clinical Research Associate, Oncology in Wilmington, NC, USA is $75,000 to $95,000 per year. However, this can vary depending on factors such as experience, education, and company size. Some larger companies may offer higher salaries or additional benefits such as bonuses or stock options.

AstraZeneca plc is a British-Swedish multinational pharmaceutical and biopharmaceutical company.