Clinical Research Associate

Welcome to Abbott, a global healthcare company dedicated to improving lives through the development of innovative medical solutions. We are currently seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. In this role, you will play a crucial part in the research and development of cutting-edge medical products that will make a meaningful impact in the lives of patients around the world. As a Clinical Research Associate at Abbott, you will have the opportunity to work alongside a team of passionate individuals and contribute to the advancement of healthcare. We are looking for candidates who possess a strong understanding of clinical research, excellent communication and organizational skills, and a commitment to delivering high-quality results. If you are driven, dedicated, and eager to make a difference, we encourage you to apply for this exciting opportunity at Abbott.

1. Conduct clinical research: The primary responsibility of the Clinical Research Associate is to conduct clinical research in accordance with established protocols and regulations.
2. Monitor clinical trials: Monitor the progress of clinical trials, ensuring that they are conducted according to established protocols and regulations, and that data is collected accurately and efficiently.
3. Coordinate with study sites: Collaborate with study sites to ensure smooth and timely execution of clinical trials, including scheduling visits, reviewing study documents, and providing support and guidance.
4. Maintain study documentation: Responsible for maintaining accurate and complete documentation of all study-related activities, including participant records, study logs, and regulatory documents.
5. Ensure compliance: Ensure compliance with all applicable regulations and guidelines, as well as Abbott's internal policies and procedures.
6. Communicate with study team: Communicate regularly with the study team to provide updates on trial progress, identify and troubleshoot any issues, and make recommendations for improvement.
7. Data management: Responsible for managing and analyzing clinical trial data, maintaining data integrity, and preparing reports for review by the study team.
8. Conduct site visits: Conduct regular site visits to monitor study progress, answer questions, and provide training and support to study staff.
9. Participate in study meetings: Participate in study team meetings to discuss trial progress, identify areas for improvement, and make recommendations for future studies.
10. Maintain ethical standards: Adhere to ethical standards and guidelines in all aspects of clinical research, including patient confidentiality and informed consent.
11. Train study staff: Provide training and guidance to study staff on study protocols, procedures, and regulations.
12. Stay updated on industry developments: Stay up-to-date on industry developments and changes in regulations to ensure compliance and improve study processes.
13. Contribute to study design: Provide input and recommendations for study design and protocol development.
14. Quality control: Conduct quality control checks on study data and documentation to ensure accuracy and completeness.
15. Participate in audits and inspections: Assist with audits

According to JobzMall, the average salary range for a Clinical Research Associate in Alameda, CA, USA is $89,000 to $105,000 per year. This can vary depending on factors such as experience, education, and specific job duties. Some CRAs may also receive bonuses or other benefits as part of their compensation package.

From removing the regular pain of finger sticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s blood donations to ensure a healthy supply, our purpose is to make the world a better place by bringing life-changing health technologies to the people who need them. That’s our commitment to helping you live your best life.