AstraZeneca Hiring Clinical Research Associate
Position: Clinical Research Associate
Organization: AstraZeneca
- Location: Bengaluru East, Karnataka, India
- Experience Required: 1 to 2 Years
- Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
- Salary: Not disclosed
About AstraZeneca
AstraZeneca is a global, science-led biopharmaceutical company committed to the discovery, development, and commercialization of prescription medicines that address some of the world’s most serious diseases. As one of the world’s leading pharmaceutical companies, AstraZeneca offers an environment where innovation and entrepreneurship thrive. If you’re passionate about science and eager to make a difference, AstraZeneca is the place for you.
Job Description: Clinical Research Associate (CRA)
The Clinical Research Associate (CRA) at AstraZeneca will play a critical role in the local delivery of oncology studies. The primary focus will be on recruitment and quality data collection at assigned sites. This role involves collaboration with other CRAs, the Local Study Team, and Local Study Managers to ensure timely and efficient study delivery.
Key Responsibilities
- Investigator Selection: Contribute to the selection of potential investigators for clinical trials.
- Study Start-Up & Maintenance: Responsible for study start-up and ongoing regulatory maintenance, including site qualification visits and document management.
- Training & Support: Train, support, and advise investigators and site staff on study-related matters to ensure compliance with AstraZeneca procedures and local regulations.
- Compliance Monitoring: Ensure that sites are inspection-ready and compliant with ICH-GCP Good Clinical Practice training requirements.
- Site Performance Monitoring: Regularly monitor site performance and address any study-related issues.
- Site Visits: Perform monitoring visits, including source data review and case report form review, ensuring that data is accurate and complete.
- Serious Adverse Event Reporting: Ensure accurate and timely reporting of Serious Adverse Events (SAEs) as per AstraZeneca and regulatory guidelines.
- Documentation: Assist sites in maintaining inspection-ready documentation throughout the study.
- Collaboration: Collaborate with local stakeholders for the successful delivery of site studies.
- Innovation: Support the implementation of innovative processes and technologies to enhance study efficiency.
Qualifications
To be successful in this role, the following qualifications are required:
- Educational Background: Bachelor’s degree in a related discipline, preferably in life sciences.
- Knowledge of Guidelines: Excellent understanding of ICH-GCP guidelines and basic knowledge of GMP/GDP.
- Clinical Study Management: Good understanding of clinical study management and drug development processes.
- Attention to Detail: Strong attention to detail with excellent written and verbal communication skills.
- Interpersonal Skills: Good collaboration, negotiation, and interpersonal skills.
- Travel Requirements: Ability to travel nationally and internationally as required.
- Driving License: Must possess a valid driving license.
Why Join AstraZeneca?
At AstraZeneca, we are committed to fostering a culture of innovation and collaboration. We believe in empowering our employees to push the boundaries of science and achieve professional growth. Our inclusive environment values diversity and continuous learning, making it an ideal place to pioneer the future of healthcare.
How to Apply
If you are passionate about contributing to the advancement of science and meet the qualifications listed above, we encourage you to apply for the Clinical Research Associate position at AstraZeneca.
Application Deadline: September 30, 2024
Apply Now: Click Here to Apply
Additional Information
- Job Type: Full-time
- Location: Bengaluru East, Karnataka, India
- Travel Requirements: Yes, as needed
For more details about AstraZeneca and our commitment to science, please visit our official website.
